NO324456B1 - Fluorerte, hydrofile polymerer, anvendelse derav samt polyvalent brannbekjempelsesskumkonsentrat - Google Patents
Fluorerte, hydrofile polymerer, anvendelse derav samt polyvalent brannbekjempelsesskumkonsentrat Download PDFInfo
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- NO324456B1 NO324456B1 NO20005948A NO20005948A NO324456B1 NO 324456 B1 NO324456 B1 NO 324456B1 NO 20005948 A NO20005948 A NO 20005948A NO 20005948 A NO20005948 A NO 20005948A NO 324456 B1 NO324456 B1 NO 324456B1
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- Prior art keywords
- hydrophilic
- weight
- monomers
- residue
- carbon atoms
- Prior art date
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- 239000012141 concentrate Substances 0.000 title claims description 49
- 239000006260 foam Substances 0.000 title claims description 40
- 229920001477 hydrophilic polymer Polymers 0.000 title description 6
- 239000000178 monomer Substances 0.000 claims description 34
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- 239000004811 fluoropolymer Substances 0.000 claims description 27
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 24
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- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 239000006185 dispersion Substances 0.000 claims description 5
- 238000010526 radical polymerization reaction Methods 0.000 claims description 5
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- 239000006184 cosolvent Substances 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 238000001556 precipitation Methods 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims description 3
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
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- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
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- 125000002947 alkylene group Chemical group 0.000 claims description 2
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- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 claims description 2
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 claims description 2
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
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- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
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- 239000007810 chemical reaction solvent Substances 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
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- JHYYINIEKJKMDD-UHFFFAOYSA-N 1-ethenyl-3,3-dimethylpyrrolidin-2-one Chemical compound CC1(C)CCN(C=C)C1=O JHYYINIEKJKMDD-UHFFFAOYSA-N 0.000 description 1
- UBPXWZDJZFZKGH-UHFFFAOYSA-N 1-ethenyl-3-methylpyrrolidin-2-one Chemical compound CC1CCN(C=C)C1=O UBPXWZDJZFZKGH-UHFFFAOYSA-N 0.000 description 1
- LWWJIQWIJBMGKE-UHFFFAOYSA-N 1-ethenyl-4-methylpyrrolidin-2-one Chemical compound CC1CN(C=C)C(=O)C1 LWWJIQWIJBMGKE-UHFFFAOYSA-N 0.000 description 1
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- QUKRIOLKOHUUBM-UHFFFAOYSA-N 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl prop-2-enoate Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)CCOC(=O)C=C QUKRIOLKOHUUBM-UHFFFAOYSA-N 0.000 description 1
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- DYPSPXFRXXXUNB-UHFFFAOYSA-N 4-ethenylpyridine;hydrochloride Chemical class Cl.C=CC1=CC=NC=C1 DYPSPXFRXXXUNB-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
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- JEUCQCLOOYWQTN-UHFFFAOYSA-N [Cs]C(c1ccccc1)(c1ccccc1)c1ccccc1 Chemical compound [Cs]C(c1ccccc1)(c1ccccc1)c1ccccc1 JEUCQCLOOYWQTN-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
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- 235000021120 animal protein Nutrition 0.000 description 1
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- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
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- 238000009833 condensation Methods 0.000 description 1
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- BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
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- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000012688 inverse emulsion polymerization Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
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- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 description 1
- QRWZCJXEAOZAAW-UHFFFAOYSA-N n,n,2-trimethylprop-2-enamide Chemical compound CN(C)C(=O)C(C)=C QRWZCJXEAOZAAW-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
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- UUORTJUPDJJXST-UHFFFAOYSA-N n-(2-hydroxyethyl)prop-2-enamide Chemical compound OCCNC(=O)C=C UUORTJUPDJJXST-UHFFFAOYSA-N 0.000 description 1
- ZTUGCJNAJJDKDC-UHFFFAOYSA-N n-(3-hydroxypropyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCCCO ZTUGCJNAJJDKDC-UHFFFAOYSA-N 0.000 description 1
- ZEMHQYNMVKDBFJ-UHFFFAOYSA-N n-(3-hydroxypropyl)prop-2-enamide Chemical compound OCCCNC(=O)C=C ZEMHQYNMVKDBFJ-UHFFFAOYSA-N 0.000 description 1
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 description 1
- ZIWDVJPPVMGJGR-UHFFFAOYSA-N n-ethyl-2-methylprop-2-enamide Chemical compound CCNC(=O)C(C)=C ZIWDVJPPVMGJGR-UHFFFAOYSA-N 0.000 description 1
- ZOTWHNWBICCBPC-UHFFFAOYSA-N n-ethyl-n-methylprop-2-enamide Chemical compound CCN(C)C(=O)C=C ZOTWHNWBICCBPC-UHFFFAOYSA-N 0.000 description 1
- SWPMNMYLORDLJE-UHFFFAOYSA-N n-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
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- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/22—Esters containing halogen
- C08F220/24—Esters containing halogen containing perhaloalkyl radicals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/56—Acrylamide; Methacrylamide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F228/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur
- C08F228/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur by a bond to sulfur
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Business, Economics & Management (AREA)
- Emergency Management (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Fire-Extinguishing Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9806941A FR2779436B1 (fr) | 1998-06-03 | 1998-06-03 | Polymeres hydrophiles fluores |
| PCT/FR1999/001236 WO1999062972A1 (fr) | 1998-06-03 | 1999-05-31 | Polymeres hydrophiles fluores |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20005948D0 NO20005948D0 (no) | 2000-11-24 |
| NO20005948L NO20005948L (no) | 2000-11-24 |
| NO324456B1 true NO324456B1 (no) | 2007-10-22 |
Family
ID=9526958
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20005948A NO324456B1 (no) | 1998-06-03 | 2000-11-24 | Fluorerte, hydrofile polymerer, anvendelse derav samt polyvalent brannbekjempelsesskumkonsentrat |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6521730B1 (ko) |
| EP (1) | EP1084164B1 (ko) |
| JP (1) | JP4598951B2 (ko) |
| KR (1) | KR100576586B1 (ko) |
| CN (1) | CN1142954C (ko) |
| AU (1) | AU3832499A (ko) |
| BR (1) | BR9910838B1 (ko) |
| CA (1) | CA2334093C (ko) |
| DE (1) | DE69933867T2 (ko) |
| ES (1) | ES2276518T3 (ko) |
| FR (1) | FR2779436B1 (ko) |
| NO (1) | NO324456B1 (ko) |
| WO (1) | WO1999062972A1 (ko) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2816622A1 (fr) * | 2000-11-15 | 2002-05-17 | Atofina | Copolymeres fluores pour le traitement hydrophobe et oleophobe des materiaux de construction |
| US7049046B2 (en) * | 2004-03-30 | 2006-05-23 | Eastman Kodak Company | Infrared absorbing compounds and their use in imageable elements |
| CN1639640A (zh) * | 2002-03-01 | 2005-07-13 | E·I·内穆尔杜邦公司 | 用于显微平版印刷的氟化共聚物 |
| WO2005100421A1 (ja) * | 2004-04-15 | 2005-10-27 | Daikin Industries, Ltd. | 含フッ素重合体および処理剤組成物 |
| JP4997708B2 (ja) * | 2005-03-08 | 2012-08-08 | Ｄｉｃ株式会社 | フッ素化アルキル基含有オリゴマーの製造方法 |
| EP1939222B2 (en) * | 2005-10-17 | 2019-09-04 | AGC Inc. | Process for producing an AQUEOUS POLYTETRAFLUOROETHYLENE EMULSION, AND POLYTETRAFLUOROETHYLENE FINE POWDER AND POROUS MATERIAL PRODUCED FROM THE SAME |
| US7494511B2 (en) * | 2006-05-08 | 2009-02-24 | E.I. Du Pont De Nemours And Company | Hydrophilic stain release agents |
| DE602007003186D1 (de) * | 2007-03-21 | 2009-12-24 | Du Pont | Fluorobetain-copolymer und Löschschaumkonzentrate daraus |
| KR100984491B1 (ko) * | 2008-01-15 | 2010-10-01 | 한국패션산업연구원 | 스마트 의복 및 그 제조방법 |
| CN102318045B (zh) * | 2008-02-14 | 2014-08-06 | 马克斯半导体股份有限公司 | 改良式击穿电压的边缘端点 |
| CA2730971A1 (en) * | 2008-07-18 | 2010-01-21 | 3M Innovative Properties Company | Cationic fluorinated polymer compositions and methods for treating hydrocarbon-bearing formations using the same |
| US8563672B2 (en) * | 2010-12-17 | 2013-10-22 | E I Du Pont De Nemours And Company | Process for producing fluorinated copolymers of (meth)acrylates and (meth)acrylic acid amine complexes |
| CN102206298B (zh) * | 2011-04-21 | 2013-01-23 | 北京化工大学 | 一种提高高分子类化学固沙剂固沙层渗水速率且降低吸水率的聚合物、制备方法及应用 |
| CN104395363A (zh) * | 2012-06-29 | 2015-03-04 | 株式会社尼欧斯 | (甲基)丙烯酸酯系共聚物、抗菌剂、赋予抗菌性的树脂组合物和赋予抗静电性的树脂组合物 |
| US9956447B2 (en) * | 2012-09-25 | 2018-05-01 | Tyco Fire & Security Gmbh | Perfluoroalkyl functionalized polyacrylamide for alcohol resistant-aqueous film-forming foam (AR-AFFF) formulation |
| EP2920271A4 (en) | 2012-11-19 | 2016-05-25 | 3M Innovative Properties Co | METHOD FOR CONTACTING CARBONATED FORMATIONS WITH FLUORINATED IONIC POLYMERS |
| WO2014097309A1 (en) | 2012-12-17 | 2014-06-26 | Asian Paints Ltd. | Stimuli responsive self cleaning coating |
| KR101654579B1 (ko) * | 2016-04-11 | 2016-09-06 | 주식회사 라인안전산업 | 소화성능이 우수한 강화액 소화약제 및 그 제조방법 |
| CN106964300B (zh) * | 2017-03-23 | 2018-11-27 | 龙岩思康特种化学品有限公司 | 一种全氟聚醚表面活性剂及其制备方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3336269A (en) * | 1964-04-07 | 1967-08-15 | Hercules Inc | Preparation of acrylamide-type water-soluble polymers |
| DE1301532B (de) | 1966-01-21 | 1969-08-21 | Cassella Farbwerke Mainkur Ag | Verfahren zur Herstellung von festen, wasserloeslichen Homo- oder Copolymerisaten des Acrylamids oder Methacrylamids |
| DE1952585A1 (de) | 1968-10-21 | 1970-04-23 | Air Prod & Chem | Fluorhaltiges Mischpolymerisat |
| US3838753A (en) | 1970-12-21 | 1974-10-01 | Bendix Corp | Disc brake caliper and mounting structure |
| US4127711A (en) * | 1977-03-31 | 1978-11-28 | E. I. Du Pont De Nemours And Company | Fluorine-containing terpolymers |
| 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 |
| JPS5932471A (ja) | 1982-08-16 | 1984-02-21 | ダイキン工業株式会社 | 消火用水性組成物 |
| JPS5988166A (ja) * | 1982-11-10 | 1984-05-22 | ダイキン工業株式会社 | 消火剤 |
| JPS60210613A (ja) | 1984-04-03 | 1985-10-23 | Fuji Photo Film Co Ltd | 写真感光材料 |
| DE3701408A1 (de) * | 1987-01-20 | 1988-07-28 | Bayer Ag | Copolymerisate aus n-vinylamiden und perfluoralkylgruppen enthaltenden ethylenisch ungesaettigten verbindungen, ein verfahren zu ihrer herstellung und ihre verwendung |
| US5010141A (en) * | 1989-10-25 | 1991-04-23 | Ciba-Geigy Corporation | Reactive silicone and/or fluorine containing hydrophilic prepolymers and polymers thereof |
| US5496475A (en) * | 1992-10-30 | 1996-03-05 | Ciba-Geigy Corporation | Low viscosity polar-solvent fire-fighting foam compositions |
| FR2739295A1 (fr) * | 1995-09-28 | 1997-04-04 | Atochem Elf Sa | Emulseurs anti-incendies polyvalents |
| WO1997045167A1 (en) * | 1996-05-31 | 1997-12-04 | Minnesota Mining And Manufacturing Company | Fire-fighting agents containing polysaccharides and fluorochemical oligomeric surfactants |
| FR2756830B1 (fr) * | 1996-12-09 | 1999-02-26 | Atochem Elf Sa | Polymeres hydrophiles fluores |
| FR2785904B1 (fr) * | 1998-11-13 | 2000-12-15 | Atochem Elf Sa | Polymeres fluores par polymerisation en miniemulsion |
-
1998
- 1998-06-03 FR FR9806941A patent/FR2779436B1/fr not_active Expired - Fee Related
-
1999
- 1999-05-31 EP EP99920927A patent/EP1084164B1/fr not_active Expired - Lifetime
- 1999-05-31 KR KR1020007013669A patent/KR100576586B1/ko not_active IP Right Cessation
- 1999-05-31 BR BRPI9910838-0A patent/BR9910838B1/pt not_active IP Right Cessation
- 1999-05-31 DE DE69933867T patent/DE69933867T2/de not_active Expired - Lifetime
- 1999-05-31 JP JP2000552179A patent/JP4598951B2/ja not_active Expired - Fee Related
- 1999-05-31 CN CNB998093602A patent/CN1142954C/zh not_active Expired - Fee Related
- 1999-05-31 WO PCT/FR1999/001236 patent/WO1999062972A1/fr active IP Right Grant
- 1999-05-31 US US09/701,788 patent/US6521730B1/en not_active Expired - Fee Related
- 1999-05-31 AU AU38324/99A patent/AU3832499A/en not_active Abandoned
- 1999-05-31 CA CA2334093A patent/CA2334093C/en not_active Expired - Fee Related
- 1999-05-31 ES ES99920927T patent/ES2276518T3/es not_active Expired - Lifetime
-
2000
- 2000-11-24 NO NO20005948A patent/NO324456B1/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR20010071382A (ko) | 2001-07-28 |
| NO20005948D0 (no) | 2000-11-24 |
| EP1084164B1 (fr) | 2006-11-02 |
| JP2002517530A (ja) | 2002-06-18 |
| AU3832499A (en) | 1999-12-20 |
| ES2276518T3 (es) | 2007-06-16 |
| CN1142954C (zh) | 2004-03-24 |
| NO20005948L (no) | 2000-11-24 |
| FR2779436B1 (fr) | 2000-07-07 |
| US6521730B1 (en) | 2003-02-18 |
| DE69933867D1 (de) | 2006-12-14 |
| CA2334093A1 (en) | 1999-12-09 |
| DE69933867T2 (de) | 2007-06-21 |
| BR9910838B1 (pt) | 2009-01-13 |
| BR9910838A (pt) | 2001-05-08 |
| EP1084164A1 (fr) | 2001-03-21 |
| CN1311803A (zh) | 2001-09-05 |
| WO1999062972A1 (fr) | 1999-12-09 |
| CA2334093C (en) | 2010-09-21 |
| FR2779436A1 (fr) | 1999-12-10 |
| JP4598951B2 (ja) | 2010-12-15 |
| KR100576586B1 (ko) | 2006-05-04 |
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