EP0885952A1 - Composition de nettoyage et de dégraissage sans point d'éclair - Google Patents
Composition de nettoyage et de dégraissage sans point d'éclair Download PDFInfo
- Publication number
- EP0885952A1 EP0885952A1 EP98111117A EP98111117A EP0885952A1 EP 0885952 A1 EP0885952 A1 EP 0885952A1 EP 98111117 A EP98111117 A EP 98111117A EP 98111117 A EP98111117 A EP 98111117A EP 0885952 A1 EP0885952 A1 EP 0885952A1
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- EP
- European Patent Office
- Prior art keywords
- composition according
- compound
- organic compound
- weight
- composition
- 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.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 65
- 238000004140 cleaning Methods 0.000 title claims abstract description 10
- 238000005238 degreasing Methods 0.000 title claims abstract description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 150000001924 cycloalkanes Chemical class 0.000 claims abstract description 13
- 150000001335 aliphatic alkanes Chemical class 0.000 claims abstract description 9
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical class ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002576 ketones Chemical class 0.000 claims abstract description 6
- RIQRGMUSBYGDBL-UHFFFAOYSA-N 1,1,1,2,2,3,4,5,5,5-decafluoropentane Chemical compound FC(F)(F)C(F)C(F)C(F)(F)C(F)(F)F RIQRGMUSBYGDBL-UHFFFAOYSA-N 0.000 claims abstract description 5
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims abstract 4
- 150000002894 organic compounds Chemical class 0.000 claims description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 11
- -1 ether alcohols Chemical class 0.000 claims description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 10
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical group CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 claims description 5
- 239000012736 aqueous medium Substances 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- PQMAKJUXOOVROI-UHFFFAOYSA-N 2,2,3,3,5,5,6,6-octafluoro-4-(trifluoromethyl)morpholine Chemical compound FC(F)(F)N1C(F)(F)C(F)(F)OC(F)(F)C1(F)F PQMAKJUXOOVROI-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 4
- ZJIJAJXFLBMLCK-UHFFFAOYSA-N perfluorohexane Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F ZJIJAJXFLBMLCK-UHFFFAOYSA-N 0.000 claims description 4
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- 229920001774 Perfluoroether Polymers 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- UJBOOUHRTQVGRU-UHFFFAOYSA-N 3-methylcyclohexan-1-one Chemical compound CC1CCCC(=O)C1 UJBOOUHRTQVGRU-UHFFFAOYSA-N 0.000 description 2
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
- WNHVGQQCXWXANA-UHFFFAOYSA-N 1,1,2-triethylcyclohexane Chemical class CCC1CCCCC1(CC)CC WNHVGQQCXWXANA-UHFFFAOYSA-N 0.000 description 1
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 description 1
- GCYUJISWSVALJD-UHFFFAOYSA-N 1,1-diethylcyclohexane Chemical class CCC1(CC)CCCCC1 GCYUJISWSVALJD-UHFFFAOYSA-N 0.000 description 1
- DPGQSDLGKGLNHC-UHFFFAOYSA-N 1,1-diethylcyclopentane Chemical class CCC1(CC)CCCC1 DPGQSDLGKGLNHC-UHFFFAOYSA-N 0.000 description 1
- VYJNCGOCKAPHLC-UHFFFAOYSA-N 1,1-dipropylcyclohexane Chemical class CCCC1(CCC)CCCCC1 VYJNCGOCKAPHLC-UHFFFAOYSA-N 0.000 description 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical class C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- CUVLMZNMSPJDON-UHFFFAOYSA-N 1-(1-butoxypropan-2-yloxy)propan-2-ol Chemical compound CCCCOCC(C)OCC(C)O CUVLMZNMSPJDON-UHFFFAOYSA-N 0.000 description 1
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 description 1
- ZGERHTZOISZNPV-UHFFFAOYSA-N 1-butyl-1-ethylcyclohexane Chemical class CCCCC1(CC)CCCCC1 ZGERHTZOISZNPV-UHFFFAOYSA-N 0.000 description 1
- LEAZMNSJMNFPHJ-UHFFFAOYSA-N 1-butyl-1-methylcyclohexane Chemical class CCCCC1(C)CCCCC1 LEAZMNSJMNFPHJ-UHFFFAOYSA-N 0.000 description 1
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
- YPJRYQGOKHKNKZ-UHFFFAOYSA-N 1-ethyl-1-methylcyclohexane Chemical class CCC1(C)CCCCC1 YPJRYQGOKHKNKZ-UHFFFAOYSA-N 0.000 description 1
- RATJFMILSANRRH-UHFFFAOYSA-N 1-ethyl-1-propylcyclohexane Chemical class CCCC1(CC)CCCCC1 RATJFMILSANRRH-UHFFFAOYSA-N 0.000 description 1
- SSOKTUYAEOXEPO-UHFFFAOYSA-N 1-methyl-1-propylcyclohexane Chemical class CCCC1(C)CCCCC1 SSOKTUYAEOXEPO-UHFFFAOYSA-N 0.000 description 1
- JSZOAYXJRCEYSX-UHFFFAOYSA-N 1-nitropropane Chemical compound CCC[N+]([O-])=O JSZOAYXJRCEYSX-UHFFFAOYSA-N 0.000 description 1
- 229940054273 1-propoxy-2-propanol Drugs 0.000 description 1
- FENFUOGYJVOCRY-UHFFFAOYSA-N 1-propoxypropan-2-ol Chemical compound CCCOCC(C)O FENFUOGYJVOCRY-UHFFFAOYSA-N 0.000 description 1
- GQCZPFJGIXHZMB-UHFFFAOYSA-N 1-tert-Butoxy-2-propanol Chemical compound CC(O)COC(C)(C)C GQCZPFJGIXHZMB-UHFFFAOYSA-N 0.000 description 1
- OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical class FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229940093475 2-ethoxyethanol Drugs 0.000 description 1
- HIVFIUIKABOGIO-UHFFFAOYSA-N 2-ethyl-1,1-dimethylcyclohexane Chemical class CCC1CCCCC1(C)C HIVFIUIKABOGIO-UHFFFAOYSA-N 0.000 description 1
- BTZVKSVLFLRBRE-UHFFFAOYSA-N 2-methoxypropyl acetate Chemical compound COC(C)COC(C)=O BTZVKSVLFLRBRE-UHFFFAOYSA-N 0.000 description 1
- LFSAPCRASZRSKS-UHFFFAOYSA-N 2-methylcyclohexan-1-one Chemical compound CC1CCCCC1=O LFSAPCRASZRSKS-UHFFFAOYSA-N 0.000 description 1
- 101100117972 Caenorhabditis elegans sdf-9 gene Proteins 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- FJOGZSYFGOIRQZ-UHFFFAOYSA-N acetic acid ethene propane-1,2-diol Chemical compound C(C)(=O)O.C(C(C)O)O.C=C FJOGZSYFGOIRQZ-UHFFFAOYSA-N 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004148 curcumin Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- NKDDWNXOKDWJAK-UHFFFAOYSA-N dimethoxymethane Chemical compound COCOC NKDDWNXOKDWJAK-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 description 1
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- MQWCXKGKQLNYQG-UHFFFAOYSA-N methyl cyclohexan-4-ol Natural products CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- VLZLOWPYUQHHCG-UHFFFAOYSA-N nitromethylbenzene Chemical compound [O-][N+](=O)CC1=CC=CC=C1 VLZLOWPYUQHHCG-UHFFFAOYSA-N 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- HTSABYAWKQAHBT-UHFFFAOYSA-N trans 3-methylcyclohexanol Natural products CC1CCCC(O)C1 HTSABYAWKQAHBT-UHFFFAOYSA-N 0.000 description 1
- DECPGQLXYYCNEZ-UHFFFAOYSA-N tris(6-methylheptyl) phosphite Chemical compound CC(C)CCCCCOP(OCCCCCC(C)C)OCCCCCC(C)C DECPGQLXYYCNEZ-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/024—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5036—Azeotropic mixtures containing halogenated solvents
- C11D7/5068—Mixtures of halogenated and non-halogenated solvents
- C11D7/509—Mixtures of hydrocarbons and oxygen-containing solvents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5013—Organic solvents containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
- C23G5/00—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents
- C23G5/02—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents
- C23G5/028—Cleaning or de-greasing metallic material by other methods; Apparatus for cleaning or de-greasing metallic material with organic solvents using organic solvents containing halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/16—Metals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/263—Ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/264—Aldehydes; Ketones; Acetals or ketals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/28—Organic compounds containing halogen
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3281—Heterocyclic compounds
Definitions
- the present invention relates to a composition for cleaning and cold degreasing of solid surfaces in a non-aqueous medium, said composition comprising at least one mixture of alkanes or cycloalkanes, at least one halogenated organic compound, in particular fluorinated or perfluorinated and at least one organic compound comprising one or more functions oxygenated.
- This composition can be used in particular for applications of degreasing of solid surfaces such as metal parts, cement, ceramic, glass, synthetic materials having been soiled by oils or greases for machining and / or their temporary protection.
- This composition can also be used for defluxing printed circuits. This defluxing operation consists in eliminating the flow of welding.
- hydrocarbons and mainly chlorinated solvents such as in particular 1,1,1-trichloroethane known in the art under the designation T 111, chlorofluoroalkanes such as 1,1,2-trichloro-1,2,2-trifluoroethane known in the trade under the designation F113 and hydrochlorofluoroalkanes (HCFC) such than 1,1-dichloro-1-fluoroethane (141-b).
- chlorinated, fluorochlorinated and hydrochlorofluorocarbon compounds are believed to be responsible for the shrinking layer stratospheric ozone which provides protection against certain radiations.
- a cold cleaning and degreasing composition for a solid surface in a non-aqueous medium characterized in that it consists of at least one organic compound (A) chosen from the group consisting of perfluoro- (N -alkylmorpholines), n-tridecafluorohexane (C 6 F 13 H), 2,3-dihydrodecafluoropentane (C 5 H 2 F 10 , 4310 mee), 3,3,4-trihydroheptafluorobutane (C 4 F 7 H 13 , 347 mcf), 2,2,4,4,4-pentahydropentafluorobutane (C 4 F 5 H 5 , 365 mcf), perfluoroalkanes, hydrofluoroalkenes, chloromethanes, fluorinated ethers, at least one mixture of alkanes or cycloalkanes (B), and at least one organic compound (C) chosen from the group consisting of ketones
- Rf and R 1 f which are identical or different, represent a linear or branched perfluorinated aliphatic radical, having a carbon number ranging from 1 to 4, n is a number ranging from 0 to 8, and the symbol F inside of the ring means that the saturated ring is completely fluorinated, that is to say that all of the carbon atoms are linked to fluorine atoms (or to R 1 f).
- perfluoroalkanes which can be used according to the invention, mention may be made of n-perfluorohexane (C 6 F 14 ).
- fluorinated ethers which can be used according to the present invention, mention may be made of n-nonafluorobutylmethyl ether (C 4 H 9 OCH 3 ).
- chloromethanes which can be used according to the present invention, mention may be made of methylene chloride CH 2 Cl 2 .
- isoparaffinic solvents sold by TOTAL under the names ISANE IP 155 and ISANE IP 165, the ISOPAR G and ISOPAR E oil cuts marketed by the company EXXON Chemical.
- mixtures of (alkyl) cycloalkanes obtained by catalytic hydrogenation of petroleum fractions consisting of compounds aromatics such as in particular, alkylbenzenes and divinylbenzenes and cyclic olefins.
- the mixtures of (alkyl) cycloalkanes thus obtained are essentially made up of saturated cyclic hydrocarbons which may have one or more alkyl radicals having from 1 to 4 carbon atoms.
- diethylcyclohexanes mixture of isomers 1,2, 1,3 and 1,4, cis and trans
- mixtures containing two or more of the following compounds: methylethylcyclohexanes, methylpropylcyclohexanes, ethylpropylcyclohexanes, dipropylcyclohexanes, methylbutylcyclohexanes, ethylbutylcyclohexanes.
- diethylcyclopentanes mono, di, and triethylcyclohexanes, ethyldimethylcyclohexanes, cyclooctane.
- naphthenic solvents sold by EXXON CHEMICAL under the name NAPPAR 10.
- ether alcohols and derivatives which can be used according to the present invention, mention may be made of methoxypropanol, 1-ethoxy-2-propanol, 1-propoxy-2-propanol, 1-n-butoxy-2-propanol, 1-tert-butoxy-2-propanol, 2-methoxyethanol, 2-ethoxyethanol, propylene glycol acetate methyl ether, acetate ethylene propylene glycol, ethylene glycol methyl ether acetate, di (propylene glycol) monomethyleter, di (propylene glycol) butyl ether.
- the composition can comprise from 1% to 40% by weight, and preferably from 1% to 25% by weight of compound (A), 60% to 98% by weight and preferably 75% to 98% by weight of a mixture of alkanes or cycloalkanes (B) and from 1% to 15% by weight and, preferably from 1% to 10% by weight of compound (C).
- composition according to the present invention can be used in cold degreasing applications in non-aqueous medium, solid surfaces such as metal parts, cement, glass, plastics having been contaminated with oils or greases used during operations machining and / or their temporary protection.
- composition can be used in so-called “non-closed” applications such as cleaning with a brush, cloth or as a spray.
- the composition according to the invention can be packaged in a non-flammable aerosol.
- a mixture comprising of 25% at 35% by weight of the composition according to the invention and from 75% to 65% by weight of a propellant, after the casing has been certified.
- propellants usable in such an application we include nitrogen, carbon dioxide, heptafluoropropane (227 ea), tetrafluoroethane (134 a) containing about 4% by volume of dimethyl ether.
- composition can be stabilized.
- the presence of an alcohol function may in the presence of light metals, lead to evolutionary reactions undesirable hydrogen that could jeopardize installation by explosion.
- derivatives may be used nitrates such as nitromethane, nitroethane, nitropropane, nitrotoluene; ethers or acetals such as dimethoxymethane, 1,3-dioxolane, dimethoxyethane; amines such as triethylamine, dipropylamine, dimethylamine; phosphorus derivatives such as triisodecylphoshite, triisooctylphosphite.
- the composition can also contain one or more masking agents smell.
- composition according to the invention has the advantage of not having flash point according to ASTM D3828 and can be easily removed after the degreasing operation.
- the flash points of the compositions are determined according to the standard ASTM D 56.
- compositions are effective for cleaning greasy soiling on cleanable surfaces.
- N means that there is no flash point according to ASTM D3828.
- CONSTITUENTS OF THE COMPOSITION EXAMPLES 1 2 3 4 5 6 7 8 9 10 11 12 13 ISO G 100 90 85 80 80 90 80 88 88 ISO E 100 90 62 60 nC 6 F 13 H 10 nC 6 -F 14 2 C 5 F 11 NO 15 5 2 5 nC 4 F 9 CH CH 2 15 5 CH 2 Cl 2 15 2 5 EAK 5 5 5 5 5 5 5 5 MP 5 DPM 8 8 5 C 5 H 2 F 10 30 C 4 H 9 OCH 3 35 Flash point (° C) 42 NOT NOT NOT NOT NOT NOT NOT NOT NOT 11 NOT NOT NOT NOT NOT NOT NOT
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
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Abstract
Description
CONSTITUANTS DE LA COMPOSITION | EXEMPLES | ||||||||||||
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | |
ISO G | 100 | 90 | 85 | 80 | 80 | 90 | 80 | 88 | 88 | ||||
ISO E | 100 | 90 | 62 | 60 | |||||||||
n-C6F13H | 10 | ||||||||||||
n-C6-F14 | 2 | ||||||||||||
C5F11NO | 15 | 5 | 2 | 5 | |||||||||
n-C4F9CH=CH2 | 15 | 5 | |||||||||||
CH 2 Cl 2 | 15 | 2 | 5 | ||||||||||
EAK | 5 | 5 | 5 | 5 | 5 | 5 | 5 | ||||||
MP | 5 | ||||||||||||
DPM | 8 | 8 | 5 | ||||||||||
C5H2F10 | 30 | ||||||||||||
C 4 H 9 OCH 3 | 35 | ||||||||||||
Point d'éclair (°C) | 42 | N | N | N | N | N | N | N | N | 11 | N | N | N |
Claims (24)
- Composition de nettoyage et de dégraissage à froid en milieu non aqueux, caractérisée en ce qu'elle est constituée par au moins un composé organique (A) choisi dans le groupe constitué par les perfluoro-(N-alkylmorpholines), le n-tridécafluorohexane (n-C6F13H, le 2,3-dihydrodécafluoropentane (C5H2F10, 4310 mee), le 3,3,4-trihydroheptafluorobutane (C4F7H13, 347 mcf), le 2,2,4,4,4-pentahydropentafluorobutane (C4F5H5, 365 mcf), les perfluoroalcanes, les hydrofluoroalcènes, les chloromethanes, les étherfluorés ; au moins un mélange d'alcanes ou de cycloalcanes (B) et au moins un composé organique (C) choisi dans le groupe constitué par les cétones, les étheralcools et dérivés et en ce que ladite composition ne présente pas de point d'éclair selon la norme ASTM D3828.
- Composition selon la revendication 1, caractérisée en ce que le composé organique (A) est une perfluoro-(N-alkylmorpholine) de formule dans laquelle Rf et R1f, identiques ou différents, représentent un radical aliphatique perfluoré, linéraire ou ramifié ayant un nombre de carbone allant de 1 à 4 et n est nombre allant de 0 à 8.
- Composition selon la revendication 1, caractérisée en ce que le composé (A) est le 2,3-dihydrodécafluoropentane (C5H2F10, 4310 mec).
- Composition selon la revendication 1, caractérisée en ce que le composé A est le n-tridécafluorohexane (n-C6F13H).
- Composition selon la revendicaiton 1, caractérisée en ce que le composé (A) est un perfluoroalcane.
- Composition selon la revendication 6, caractérisée en ce que le perfluoroalcane est le n-perfluorohexane (n-C6F14).
- Composition selon la revendication 1, caractérisée en ce que le composé (A) est un hydrofluoroalcéne.
- Composition selon la revendication 8, caractérisée en ce que l'hydrofluoroalcéne est le n-perfluorobutyléthylène (n-C4F9-CH = CH2).
- Composition selon la revendication 1, caracérisée en ce que le composé (A) est un chlorométhane.
- Composition selon la revendication 10, caractérisée en ce que le chlorométhane est le chlorure de méthylène.
- Composition selon la revendication 1, caractérisée en ce que le composé (A) est un étherfluoré.
- Composition selon la revendication 12, caractérisée en ce que l'étherfluoré est le n-nonafluorobutylméthyléther (C4H9OCH3).
- Composition selon la revendication 1, caractérisée en ce que le mélange d'alcanes (B) est une coupe pétrolière ayant un nombre de carbone allant de 8 à 12 et, de préférence allant de 9 à 11.
- Composition selon la revendication 1, caractérisée en ce que le composé organique (C) est une cétone.
- Composition selon la revendication 15, caractérisée en ce que la cétone est l'éthylamylcétone.
- Composition selon la revendication 1, caractérisée en ce que le composé (C) est un étheralcool.
- Composition selon la revendication 17, caractérisée en ce que l'étheralcool est le méthoxypropanol.
- Composition selon la revendication 17, caractérisée en ce que l'étheralcool est le di(propylène glycol)monométhyléther.
- Composition selon l'une des revendications 1 à 19, caractérisée en ce qu'elle comprend de 1 % à 40 % en poids de composé organique (A), de 60 % à 98 % en poids d'un mélange d'alcanes ou de cycloalcanes (B) et, de 1 % à 15 % en poids de composé organique (C).
- Composition selon la revendication 20, caractérisée en ce qu'elle comprend de 1 % à 25 % en poids de composé organique (A), de 75 % à 98 % en poids d'un mélange d'alcanes ou de cycloalcanes (B) et, de 1 % à 10 % en poids de composé organique (C).
- Application d'une composition selon l'une des revendications 1 à 21 au nettoyage à froid en milieu non aqueux de surfaces solides.
- Application selon la revendication 22 au dégraissage des pièces métalliques.
- Application selon l'une des revendications 22 et 23 au nettoyage et/ou dégraissage en pulvérisation.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9707725 | 1997-06-20 | ||
FR9707725 | 1997-06-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0885952A1 true EP0885952A1 (fr) | 1998-12-23 |
Family
ID=9508249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98111117A Withdrawn EP0885952A1 (fr) | 1997-06-20 | 1998-06-17 | Composition de nettoyage et de dégraissage sans point d'éclair |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0885952A1 (fr) |
JP (1) | JPH1192792A (fr) |
KR (1) | KR100284347B1 (fr) |
CN (1) | CN1213697A (fr) |
CA (1) | CA2239818A1 (fr) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001016422A1 (fr) * | 1999-09-01 | 2001-03-08 | Niran Technologies, Inc. | Compositions non aqueuses non combustibles |
GB2358189A (en) * | 2000-01-11 | 2001-07-18 | Asahi Glass Co Ltd | Fluorinated carrier solvent |
WO2002064724A1 (fr) * | 2001-02-14 | 2002-08-22 | Kaneko Chemical Co., Ltd. | Compositions detergentes a base de solvants |
EP1342776A1 (fr) * | 2002-03-06 | 2003-09-10 | Asahi Glass Company Ltd. | Composition à base de solvants |
WO2006086683A2 (fr) * | 2005-02-09 | 2006-08-17 | E.I. Dupont De Nemours And Company | Compositions a base de 1,1,1,2,2,3,4,5,5,6,6,7,7,7-tetradecafluoroheptane et leurs utilisations |
WO2006130406A2 (fr) * | 2005-05-27 | 2006-12-07 | E. I. Du Pont De Nemours And Company | Compositions contenant du 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexene |
WO2007100887A2 (fr) * | 2006-02-28 | 2007-09-07 | E. I. Du Pont De Nemours And Company | Compositions azéotropiques comprenant des composés fluorés pour des applications de nettoyage |
WO2008042066A1 (fr) | 2006-09-01 | 2008-04-10 | E.I. Du Pont De Nemours And Company | Stabilisants amine pour fluoro-oléfines |
US8075796B2 (en) | 2006-09-01 | 2011-12-13 | E. I. Du Pont De Nemours And Company | Phenol stabilizers for fluoroolefins |
US8097181B2 (en) | 2006-09-01 | 2012-01-17 | E.I. Du Pont De Nemours And Company | Ascorbic acid, terephthalate and nitromethane stabilizers for fluoroolefins |
US8101094B2 (en) | 2006-09-01 | 2012-01-24 | E. I. Du Pont De Nemours And Company | Terpene, terpenoid, and fullerene stabilizers for fluoroolefins |
US8394286B2 (en) | 2006-09-01 | 2013-03-12 | E I Du Pont De Nemours And Company | Thiol and thioether stabilizers for fluoroolefins |
US8529786B2 (en) | 2006-09-01 | 2013-09-10 | E I Du Pont De Nemours And Company | Phosphorus-containing stabilizers for fluoroolefins |
US8535555B2 (en) | 2006-09-01 | 2013-09-17 | E I Du Pont De Nemours And Company | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
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JP4826014B2 (ja) * | 2000-01-11 | 2011-11-30 | 旭硝子株式会社 | フッ素系希釈溶剤 |
US7279451B2 (en) * | 2002-10-25 | 2007-10-09 | Honeywell International Inc. | Compositions containing fluorine substituted olefins |
KR101444799B1 (ko) * | 2007-12-31 | 2014-09-29 | 동원이엠 주식회사 | 난연성 고리형 탄화수소 세정용제 조성물 및 그 제조방법 |
CN102227395A (zh) * | 2008-11-13 | 2011-10-26 | 苏威氟有限公司 | 氢氟烯烃、氢氟烯烃的制造以及使用氢氟烯烃的方法 |
JP6118450B1 (ja) * | 2016-11-10 | 2017-04-19 | 株式会社カネコ化学 | 洗浄用組成物 |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0431458A1 (fr) * | 1989-12-07 | 1991-06-12 | Daikin Industries, Limited | Composition de nettoyage |
WO1994023091A1 (fr) * | 1993-04-01 | 1994-10-13 | Minnesota Mining And Manufacturing Company | Compositions azeotropiques contenant du cycloaminoether perfluore |
WO1994023008A1 (fr) * | 1993-04-01 | 1994-10-13 | Minnesota Mining And Manufacturing Company | Compositions azeotropiques |
US5403514A (en) * | 1991-10-07 | 1995-04-04 | Canon Kabushiki Kaisha | Solvent composition and water-repellent/oil-repellent composition using the same |
JPH07113098A (ja) * | 1993-10-18 | 1995-05-02 | A G Technol Kk | 擬共沸溶剤組成物 |
US5454969A (en) * | 1993-06-18 | 1995-10-03 | Fields; Paul B. | Cleaning fluids |
EP0675193A1 (fr) * | 1993-10-18 | 1995-10-04 | Ag Technology Co. Ltd. | Composition de solvants melanges |
WO1996033261A1 (fr) * | 1995-04-20 | 1996-10-24 | Elf Atochem S.A. | Composition de nettoyage a froid a base d'alcanes ou de cycloalcanes et d'un compose organique comprenant une fonction cetone |
US5750488A (en) * | 1996-01-04 | 1998-05-12 | Crc Industries, Inc. | Fluorinated cleaning solvents |
-
1998
- 1998-06-17 EP EP98111117A patent/EP0885952A1/fr not_active Withdrawn
- 1998-06-19 CA CA002239818A patent/CA2239818A1/fr not_active Abandoned
- 1998-06-19 KR KR1019980023161A patent/KR100284347B1/ko not_active IP Right Cessation
- 1998-06-20 CN CN98117536A patent/CN1213697A/zh active Pending
- 1998-06-22 JP JP10211730A patent/JPH1192792A/ja active Pending
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0431458A1 (fr) * | 1989-12-07 | 1991-06-12 | Daikin Industries, Limited | Composition de nettoyage |
US5403514A (en) * | 1991-10-07 | 1995-04-04 | Canon Kabushiki Kaisha | Solvent composition and water-repellent/oil-repellent composition using the same |
WO1994023091A1 (fr) * | 1993-04-01 | 1994-10-13 | Minnesota Mining And Manufacturing Company | Compositions azeotropiques contenant du cycloaminoether perfluore |
WO1994023008A1 (fr) * | 1993-04-01 | 1994-10-13 | Minnesota Mining And Manufacturing Company | Compositions azeotropiques |
US5454969A (en) * | 1993-06-18 | 1995-10-03 | Fields; Paul B. | Cleaning fluids |
JPH07113098A (ja) * | 1993-10-18 | 1995-05-02 | A G Technol Kk | 擬共沸溶剤組成物 |
EP0675193A1 (fr) * | 1993-10-18 | 1995-10-04 | Ag Technology Co. Ltd. | Composition de solvants melanges |
WO1996033261A1 (fr) * | 1995-04-20 | 1996-10-24 | Elf Atochem S.A. | Composition de nettoyage a froid a base d'alcanes ou de cycloalcanes et d'un compose organique comprenant une fonction cetone |
US5750488A (en) * | 1996-01-04 | 1998-05-12 | Crc Industries, Inc. | Fluorinated cleaning solvents |
Non-Patent Citations (1)
Title |
---|
DATABASE WPI Section Ch Week 9526, Derwent World Patents Index; Class E19, AN 95-196820, XP002078350 * |
Cited By (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001016422A1 (fr) * | 1999-09-01 | 2001-03-08 | Niran Technologies, Inc. | Compositions non aqueuses non combustibles |
US6740362B2 (en) | 2000-01-11 | 2004-05-25 | Asahi Glass Company, Limited | Fluorinated carrier solvent |
GB2358189A (en) * | 2000-01-11 | 2001-07-18 | Asahi Glass Co Ltd | Fluorinated carrier solvent |
US6544595B2 (en) | 2000-01-11 | 2003-04-08 | Asahi Glass Company, Limited | Fluorinated carrier solvent |
GB2358189B (en) * | 2000-01-11 | 2004-08-11 | Asahi Glass Co Ltd | Method for coating a substance with a lubricant |
US7462591B2 (en) | 2001-02-14 | 2008-12-09 | Kaneko Chemical Co., Ltd. | Solvent composition for cleaning |
US7799750B2 (en) | 2001-02-14 | 2010-09-21 | Kaneko Chemical Co., Ltd. | Solvent composition for cleaning |
US7091170B2 (en) | 2001-02-14 | 2006-08-15 | Kaneko Chemical Co., Ltd. | Solvent composition for washing |
WO2002064724A1 (fr) * | 2001-02-14 | 2002-08-22 | Kaneko Chemical Co., Ltd. | Compositions detergentes a base de solvants |
US7053035B2 (en) | 2002-03-06 | 2006-05-30 | Asahi Glass Company, Limited | Solvent composition |
EP1342776A1 (fr) * | 2002-03-06 | 2003-09-10 | Asahi Glass Company Ltd. | Composition à base de solvants |
WO2006086683A2 (fr) * | 2005-02-09 | 2006-08-17 | E.I. Dupont De Nemours And Company | Compositions a base de 1,1,1,2,2,3,4,5,5,6,6,7,7,7-tetradecafluoroheptane et leurs utilisations |
WO2006086683A3 (fr) * | 2005-02-09 | 2007-05-18 | Du Pont | Compositions a base de 1,1,1,2,2,3,4,5,5,6,6,7,7,7-tetradecafluoroheptane et leurs utilisations |
WO2006130406A2 (fr) * | 2005-05-27 | 2006-12-07 | E. I. Du Pont De Nemours And Company | Compositions contenant du 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexene |
WO2006130406A3 (fr) * | 2005-05-27 | 2007-03-01 | Du Pont | Compositions contenant du 3,3,4,4,5,5,6,6,6-nonafluoro-1-hexene |
WO2007100887A2 (fr) * | 2006-02-28 | 2007-09-07 | E. I. Du Pont De Nemours And Company | Compositions azéotropiques comprenant des composés fluorés pour des applications de nettoyage |
WO2007100887A3 (fr) * | 2006-02-28 | 2007-11-22 | Du Pont | Compositions azéotropiques comprenant des composés fluorés pour des applications de nettoyage |
US7498296B2 (en) | 2006-02-28 | 2009-03-03 | E. I. Dupont De Nemours And Company | Azeotropic compositions comprising fluorinated compounds for cleaning applications |
US8097181B2 (en) | 2006-09-01 | 2012-01-17 | E.I. Du Pont De Nemours And Company | Ascorbic acid, terephthalate and nitromethane stabilizers for fluoroolefins |
US8663494B2 (en) | 2006-09-01 | 2014-03-04 | E I Du Pont De Nemours And Company | Terpene, terpenoid, and fullerene stabilizers for fluoroolefins |
WO2008042066A1 (fr) | 2006-09-01 | 2008-04-10 | E.I. Du Pont De Nemours And Company | Stabilisants amine pour fluoro-oléfines |
US8101094B2 (en) | 2006-09-01 | 2012-01-24 | E. I. Du Pont De Nemours And Company | Terpene, terpenoid, and fullerene stabilizers for fluoroolefins |
US8383004B2 (en) | 2006-09-01 | 2013-02-26 | E I Du Pont De Nemours And Company | Amine stabilizers for fluoroolefins |
US8394286B2 (en) | 2006-09-01 | 2013-03-12 | E I Du Pont De Nemours And Company | Thiol and thioether stabilizers for fluoroolefins |
US8496846B2 (en) | 2006-09-01 | 2013-07-30 | E I Du Pont De Nemours And Company | Phenol stabilizers for fluoroolefins |
US8529786B2 (en) | 2006-09-01 | 2013-09-10 | E I Du Pont De Nemours And Company | Phosphorus-containing stabilizers for fluoroolefins |
US8535555B2 (en) | 2006-09-01 | 2013-09-17 | E I Du Pont De Nemours And Company | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
US8075796B2 (en) | 2006-09-01 | 2011-12-13 | E. I. Du Pont De Nemours And Company | Phenol stabilizers for fluoroolefins |
US8668791B2 (en) | 2006-09-01 | 2014-03-11 | E I Du Pont De Nemours And Company | Ascorbic acid, terephthalate and nitromethane stabilizers for fluoroolefins |
US8815114B2 (en) | 2006-09-01 | 2014-08-26 | E I Du Pont De Nemours And Company | Phenol stabilizers for fluoroolefins |
US9133381B2 (en) | 2006-09-01 | 2015-09-15 | The Chemours Company Fc, Llc | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
US9777204B2 (en) | 2006-09-01 | 2017-10-03 | The Chemours Company Fc, Llc | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
US10550302B2 (en) | 2006-09-01 | 2020-02-04 | The Chemours Company Fc, Llc | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
US11130894B2 (en) | 2006-09-01 | 2021-09-28 | The Chemours Company Fc, Llc | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
US11851602B2 (en) | 2006-09-01 | 2023-12-26 | The Chemours Company Fc, Llc | Epoxide and fluorinated epoxide stabilizers for fluoroolefins |
Also Published As
Publication number | Publication date |
---|---|
KR19990007162A (ko) | 1999-01-25 |
CA2239818A1 (fr) | 1998-12-20 |
JPH1192792A (ja) | 1999-04-06 |
CN1213697A (zh) | 1999-04-14 |
KR100284347B1 (ko) | 2002-05-09 |
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