EP0265979B1 - Thickened aqueous cleaning compositions - Google Patents
Thickened aqueous cleaning compositions Download PDFInfo
- Publication number
- EP0265979B1 EP0265979B1 EP87201850A EP87201850A EP0265979B1 EP 0265979 B1 EP0265979 B1 EP 0265979B1 EP 87201850 A EP87201850 A EP 87201850A EP 87201850 A EP87201850 A EP 87201850A EP 0265979 B1 EP0265979 B1 EP 0265979B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- sulphonate
- carbon atoms
- contain
- weight
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims abstract description 92
- 238000004140 cleaning Methods 0.000 title claims abstract description 28
- 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 claims abstract description 24
- 230000008719 thickening Effects 0.000 claims abstract description 19
- 239000002253 acid Substances 0.000 claims abstract description 14
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims abstract description 11
- 150000003839 salts Chemical group 0.000 claims abstract description 11
- 239000004094 surface-active agent Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000008096 xylene Substances 0.000 claims abstract description 11
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims abstract description 10
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000000129 anionic group Chemical group 0.000 claims abstract description 9
- NIXKBAZVOQAHGC-UHFFFAOYSA-N phenylmethanesulfonic acid Chemical compound OS(=O)(=O)CC1=CC=CC=C1 NIXKBAZVOQAHGC-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000003512 tertiary amines Chemical class 0.000 claims abstract description 9
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims abstract description 5
- 230000008569 process Effects 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- 239000003760 tallow Substances 0.000 claims description 12
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 claims description 10
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 6
- 229930195735 unsaturated hydrocarbon Chemical group 0.000 claims description 6
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 5
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 8
- 230000000249 desinfective effect Effects 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 abstract description 21
- 150000001412 amines Chemical class 0.000 abstract description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 8
- 230000001747 exhibiting effect Effects 0.000 abstract description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000002304 perfume Substances 0.000 description 10
- 239000003599 detergent Substances 0.000 description 7
- -1 hydroxyl compound Chemical class 0.000 description 7
- 229960004106 citric acid Drugs 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 6
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 6
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 3
- LULAYUGMBFYYEX-UHFFFAOYSA-N 3-chlorobenzoic acid Chemical compound OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000862632 Soja Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000008043 acidic salts Chemical class 0.000 description 2
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 150000002440 hydroxy compounds Chemical class 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- GIPRGFRQMWSHAK-UHFFFAOYSA-M sodium;2-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=CC=C1S([O-])(=O)=O GIPRGFRQMWSHAK-UHFFFAOYSA-M 0.000 description 2
- KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 description 2
- XRHGYUZYPHTUJZ-UHFFFAOYSA-N 4-chlorobenzoic acid Chemical compound OC(=O)C1=CC=C(Cl)C=C1 XRHGYUZYPHTUJZ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- YASYEJJMZJALEJ-UHFFFAOYSA-N Citric acid monohydrate Chemical compound O.OC(=O)CC(O)(C(O)=O)CC(O)=O YASYEJJMZJALEJ-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 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 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- RBRXPPLNXDVMKG-GMFCBQQYSA-M bis(2-hydroxyethyl)-methyl-[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(CCO)CCO RBRXPPLNXDVMKG-GMFCBQQYSA-M 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 239000002752 cationic softener Substances 0.000 description 1
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229960002303 citric acid monohydrate Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical class [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- BGKUZGVLFHGANI-UHFFFAOYSA-M dodecyl-ethyl-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC BGKUZGVLFHGANI-UHFFFAOYSA-M 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- WSPPHMXAIHWZAH-UHFFFAOYSA-M ethyl-dimethyl-octadecylazanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC WSPPHMXAIHWZAH-UHFFFAOYSA-M 0.000 description 1
- RXHDXDIEHWVFOC-UHFFFAOYSA-M ethyl-dimethyl-octadecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC RXHDXDIEHWVFOC-UHFFFAOYSA-M 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- BZDOEVMUXJTHPS-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)hexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+]([O-])(CCO)CCO BZDOEVMUXJTHPS-UHFFFAOYSA-N 0.000 description 1
- CBLJNXZOFGRDAC-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)octadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])(CCO)CCO CBLJNXZOFGRDAC-UHFFFAOYSA-N 0.000 description 1
- OPEIOQDUOOQJEM-UHFFFAOYSA-N n,n-diethyloctadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])(CC)CC OPEIOQDUOOQJEM-UHFFFAOYSA-N 0.000 description 1
- OZYPPHLDZUUCCI-UHFFFAOYSA-N n-(6-bromopyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=CC(Br)=N1 OZYPPHLDZUUCCI-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- RJSZFSOFYVMDIC-UHFFFAOYSA-N tert-butyl n,n-dimethylcarbamate Chemical compound CN(C)C(=O)OC(C)(C)C RJSZFSOFYVMDIC-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- SZEMGTQCPRNXEG-UHFFFAOYSA-M trimethyl(octadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C SZEMGTQCPRNXEG-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
-
- 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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/34—Organic compounds containing sulfur
- C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
Definitions
- the invention relates to aqueous cleaning compositions incorporating low levels of quaternary ammonium salt or amine oxide surfactant and displaying pronounced shear thinning behaviour, i.e. exhibiting high viscosities at low rates of shear.
- This type of behaviour is of particular advantage in cleaning compositions intended to be applied to non-horizontal structural surfaces such as walls and windows and sanitary fittings such as sinks, baths, showers, wash basins and lavatories.
- the invention is especially concerned with aqueous acid-containing cleaning compositions which are commonly applied to the surfaces of sanitary fittings.
- GB 1 240 469 discloses compositions, suitable for cleaning metal, glass and painted surfaces, which compositions have a pH not higher than 7,0 and comprise (a) an inorganic acid, an organic acid or an acidic salt (b) a cationic detergent and (c) a water insoluble or partially water soluble covalent compound other than the compounds under (b) and which contains oxygen or halogen and at least one hydrocarbon chain of at least four carbon atoms.
- component (c) can more particularly be used an ester of an inorganic acid, a fatty acid or an ester of a fatty acid, a carboxylic acid ester in which the hydrocarbon chain derived from the alcohol has at least four carbon atoms, an alkyl chloride, a hydroxyl compound or substituted hydroxy compound, and the hydroxy compound is preferably water insoluble, such as a fatty alcohol, containing from 4-30 carbon atoms in at least one alkyl chain.
- cationic detergent only an amine oxide of a special structure is mentioned, which is exemplified by a large number of representatives, the actual application of quaternary ammonium salts being neither disclosed in general terms, nor in specifically exemplified representatives.
- US Patent Specification 3 997 453 discloses a stable, cold water dispersible fabric softening composition
- a stable, cold water dispersible fabric softening composition comprising from about 60 to 20% by weight of a cationic quaternary ammonium softener, an organic anionic sulfonate, the weight ratio of the cationic softener to the anionic detergent being from about 40:1 to 5:1 and wherein the anionic sulphonate being selected from amongst benzene or naphthalene sulphonate or a polyalkyl substituted aromatic sulphonate with one of the alkyl groups having not more than 18 C-atoms and each of the remaining alkyl group having not more than 2 carbon atoms.
- FR-A-2 409 303 example 98, describes a composition containing a coco dimethyl amine oxide, an amine oxide wherein R 1 is a group with 12 carbon atoms. Thickening is achieved by combining a soap and an amine oxide.
- US-A-3 892 669 discloses fabric-softening compositions which are thickened by the addition of thickeners as hydroxyethylcellulose.
- GB-A-948 396 discloses an aqueous cleaning composition which is opaque and viscous at room temperature and which contains an alkali borate, a tertiary amine oxide, one or more detergent salts of anionic organic sulfuric reaction products, a salt of a non-detergent aryl sulfonic acid hydrotrope anion, and a pyrophosphate salt.
- cleaning, desinfecting and/or odorizing agents are auxiliary detergents, acids, detergent builder salts, perfumes, antibiotics or active chlorine providing means.
- a preferred embodiment of the present invention is formed by thickened aqueous cleaning compositions having a pH of not more than 7 and preferably between 0 and 6 and more preferably between 0-4, and containing 1-15% by weight of an acid, normally occurring in cleaning compositions.
- quaternary ammonium compounds referred to under (a) are:
- a preferred group of the cationic ammonium compounds are:
- Typical examples of tertiary amine oxides referred to under (a) are:
- a preferred group of the amine oxides are:
- the amine oxide and/or quaternary ammonium compound may preferably be used in amounts from 0.1% to 5% by weight based on the total weight of the composition dependent on the viscosity and the type of the agent desired.
- a preferred embodiment of the present invention is formed by thickened compositions containing one or more salts of the specified sulphonates.
- Typical salts of the sulphonates specified under (b) are the sodium, potassium, ammonium, lower amine and alkanolamine salts, of which the sodium salts are preferred.
- Typical acids which may be applied in the compositions of the present invention are sulphuric acid, phosphoric acid, sulphamic acid, hydrochloric acid, citric acid, acetic acid, formic acid or an acidic salt of the type conventionally used in cleaning compositions, or combinations thereof in an amount of from 1-15%.
- the ratio of the weights of the quaternary ammonium compound or tertiary amine oxide to the sulphonate is in the range from 0.1-6 and preferably from 1.5-2.5 and more preferably around about 2.0.
- a preferred embodiment of the invention is formed by the thickened cleaning composition which comprises: which showed the following viscosity values at different shear rates, using a Haake Rotovisco (trade name of Haake MeBtechnik GmbH and Co, Düsseldorf, Germany) RV 100 viscosimeter.
- the thickening systems described above display a viscosity temperature relationship that has a parabolic profile with the maximum viscosity being exhibited at a temperature in the range from 0 ° C to 30 °C.
- An increase in chain length of higher alkyl chain in the quaternary ammonium ion or amine oxide in general increases the temperature at which this peak occurs while a reduction in this higher alkyl chain length and/or branching in this alkyl group, reduces the temperature at which the maximum viscosity is produced by the system.
- compositions of the present invention will be governed by the specific kind of surfactant (quaternary ammonium ion or amine oxide), kind of sulphonate, kind of acid in the composition, amount of acid electrolyte concentration in total composition, ratio of weights of the surfactant-sulphonate combinations, and counter ion of the sulphonates.
- the thickening compositions according to the present invention have however appeared to be rather insensitive to other types of ingredients occurring in the complete aqueous cleaning composition, such as perfume.
- the weight ratio of tallow trimethyl ammonium chloride and sodium xylene sulphonate in citric acid solution of 4.5% by weight (100%), i.e., 5% of hydrated citric acid, may vary from 2.0-2.5, and more preferably 2.15-2.25, while acceptable compositions for practical purposes may show ratios from 0.5-4.0 (based on 100% ingredients).
- a thickening premix composition which comprises at least:
- thickening premix compositions have appeared to be rather insensitive to the presence of other ingredients in the final cleaning composition, e.g., perfume.
- Such thickening premix compositions have been found to consist of homogeneous mixtures of components (a) and (b) and to exhibit a long storage stability. When mixed with water or an aqueous solution they display a surprising thickening effect.
- Another feature of the present invention is formed by the application of the thickened aqueous single phase compositions according to the usual methods of this specific art of cleaning non-horizontal surfaces such as walls, windows and sanitary fittings.
- Citric acid monohydrate (5.0 g) is dissolved in about 85.0 ml of demineralized water, with stirring, at 20 ° C, whereafter 2.2 g of tallow trimethyl ammonium chloride (as 50% solution Arquad T 50@) are added, followed by the addition of 1.25 g of sodium xylene sulphonate (as 40% solution), with continued stirring. The viscosity increases immediately during the addition of the sulphonate.
- the perfume may be mixed with the tallow trimethyl ammonium chloride.
- the obtained composition comprises:
- composition shows a good viscosity and is completely clear and stable at elevated temperature (40 °C). The colour does not change during storage.
- the viscosity was measured by Brookfield LVT, 60 rev/min, 230 m Pa.s (20°C). The composition did not show any cloud point on cooling down to 0 °C, and on heating up to 95 °C.
- the viscosities were measured by using a Brookfield LVT 60 rpm.
- compositions were prepared containing respectively:
- composition I was reported as becoming cloudy and thin, while composition II remained clear and had a viscosity of 190 m Pa.s. at 20 °C.
- composition II remained clear and had a viscosity of 190 m Pa.s. at 20 °C.
- the same behaviour could be observed in the case of similar compositions containing sodium cumene sulphonate or sodium toluene sulphonate, showing a rather small perfume susceptibility which permits the use of premix compositions derived from sulphonate-quaternary ammonium derivatives.
- composition II could be applied in all acids specified in Example 2.
- compositions were prepared along the lines of the process described in Example 1, starting from bis(2-hydroxy ethyl) tallowamine oxide (Aromox T12@) in amounts from 3 to 7% by weight, sodium xylene sulphonate, sodium toluene sulphonate, sodium cumene sulphonate, or secondary n-alkane sulphonates of the formulae and wherein R and R 1 represent an alkane residue of from 13-18 carbon atoms (Hostapur@ SAS wherein C 13 -n-alkanesulphonate represents 3% of the composition, C14-n-alkanesulphonate 25%, C15-n-alkanesulphonate 30%, C 16 -n-alkanesulphonate 25, C 17 -n-alkanesulphonate 15% and C 18 -n-alkanesulphonate 2%, being an example of a composition according to EP-0 137 871) in amounts of from 0-2% by weight, and hydrated citric
- compositions containing amine oxide and olefin sulphonates e.g. ELFAN OS46@ III showed inferior thickening properties as compared with combination I and moreover had an intensive yellow colour.
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Abstract
Description
- The invention relates to aqueous cleaning compositions incorporating low levels of quaternary ammonium salt or amine oxide surfactant and displaying pronounced shear thinning behaviour, i.e. exhibiting high viscosities at low rates of shear.
- This type of behaviour is of particular advantage in cleaning compositions intended to be applied to non-horizontal structural surfaces such as walls and windows and sanitary fittings such as sinks, baths, showers, wash basins and lavatories.
The invention is especially concerned with aqueous acid-containing cleaning compositions which are commonly applied to the surfaces of sanitary fittings. - It is well known that the higher the viscosity of a liquid composition, the greater will be its residence time when applied to a non-horizontal surface such as a wall. This viscosity can be increased in many ways. Especially for compositions containing a hypochlorite bleach, a variety of formulations have been proposed, but thickening systems have also been proposed for aqueous cleaning compositions of a pH not higher than 7,0 .
- GB 1 240 469, for instance, discloses compositions, suitable for cleaning metal, glass and painted surfaces, which compositions have a pH not higher than 7,0 and comprise (a) an inorganic acid, an organic acid or an acidic salt (b) a cationic detergent and (c) a water insoluble or partially water soluble covalent compound other than the compounds under (b) and which contains oxygen or halogen and at least one hydrocarbon chain of at least four carbon atoms.
- As component (c) can more particularly be used an ester of an inorganic acid, a fatty acid or an ester of a fatty acid, a carboxylic acid ester in which the hydrocarbon chain derived from the alcohol has at least four carbon atoms, an alkyl chloride, a hydroxyl compound or substituted hydroxy compound, and the hydroxy compound is preferably water insoluble, such as a fatty alcohol, containing from 4-30 carbon atoms in at least one alkyl chain.
As cationic detergent only an amine oxide of a special structure is mentioned, which is exemplified by a large number of representatives, the actual application of quaternary ammonium salts being neither disclosed in general terms, nor in specifically exemplified representatives. - US Patent Specification 3 997 453 discloses a stable, cold water dispersible fabric softening composition comprising from about 60 to 20% by weight of a cationic quaternary ammonium softener, an organic anionic sulfonate, the weight ratio of the cationic softener to the anionic detergent being from about 40:1 to 5:1 and wherein the anionic sulphonate being selected from amongst benzene or naphthalene sulphonate or a polyalkyl substituted aromatic sulphonate with one of the alkyl groups having not more than 18 C-atoms and each of the remaining alkyl group having not more than 2 carbon atoms.
- Considering the statements in US Patent Specification 3 997 453, lines 42-45 and lines 57-64 of column 1, it is clear that a person skilled in the art would only be led away from trying to use combinations of cationic quarternary compounds and an anionic sulphonate as thickening composition. A person skilled in the art was even fortified in that prejudice on account of Kunishov et al, Tr. Mezhdunar. Kongr. Paverkhn. - Akt. Veshchestvam, 7 th 1976 (publ. 1978), 3, 150-8, Nats. Komm. SSSR Poverchn. - Akt. Veschchestvam Moscow, USSR.
- From e.g. Journal of Colloid and Interface Science, vol. 57, no. 3, December 1976, 575-577; Journal of Physical Chemistry, vol. 83, no. 17, 1979, 2232-2236; Ber. Bunsenges. Phys. Chem. 85, 255-276 (1981) and ibidem 86, 37-42 (1982) a great interest appears for research relating to viscoelastic surfactant solutions, containing a quaternary ammonium compound derived from salicylic acid, m-chlorobenzoic acid and p-chlorobenzoic acid, while moreover from Journal of Colloid and Interface Science, vol. 57, no. 3, December 1976, page 576 and from Wan. L.S.C., J. Pharm. Sci. 55, 1395 (1966) it could anyhow be derived by a skilled person that the desired increase in viscosity could not generally be obtained in the pH range of from 1.6 to 2.5, depending on the organic acid to be applied with, e.g., cetyl trimethyl ammonium bromide.
- Moreover, the continued exceptional interest taken in the last few years in the rheological properties of aqueous compositions, containing quaternary ammonium ions and salicyclic acid and some sulphonates of alkyls, clearly appears from, e.g., Seifen-ole-Fetten-Wachse-111 Jg. No. 15/1985, 467-471 and 200-202 and Journal of Colloid and Interface Science, Vol. 106, No. 1, July 1985, 222-225, whereas from the European patent applications Nos. 0 144 166 and 0 137 871 it appears that people skilled in the art, when looking for alternative improved thickening systems, also began to consider the application of tertiary amine oxides in certain specific compositions.
- It will be appreciated from these two patent applications, that the former prejudice that cumene sulphonates, xylenes sulphonates or toluene sulphonates and the like were far from attractive for use in thickening compositions of aqueous solutions, continued to exist.
- More particularly, from lines 5-8 of page 3 and lines 4-25 and more particularly lines 11 and 12 of page 5 of EP 0 137 871, it appears that skilled people were primarily looking for other combinations of specific amine oxides and anionic surfactants which are substantially different from cumene sulphonate, xylene sulphonate, toluene sulphonate and which have a more complex structure and are therefore more difficult to handle. Moreover, such compounds are higher in price.
- Prior patent application EP-A-0 204 472 (not prepublished) discloses aqueous cleaning composition containing amine oxides having the formula R1 R2 R3 N-0, wherein R1 is C12-C15 group whereas applicant is claiming a cleaning composition containing amine oxides wherein R1 is a group with at least 16 carbon atoms.
- FR-A-2 409 303, example 98, describes a composition containing a coco dimethyl amine oxide, an amine oxide wherein R1 is a group with 12 carbon atoms. Thickening is achieved by combining a soap and an amine oxide.
- US-A-3 892 669 discloses fabric-softening compositions which are thickened by the addition of thickeners as hydroxyethylcellulose.
- GB-A-948 396 discloses an aqueous cleaning composition which is opaque and viscous at room temperature and which contains an alkali borate, a tertiary amine oxide, one or more detergent salts of anionic organic sulfuric reaction products, a salt of a non-detergent aryl sulfonic acid hydrotrope anion, and a pyrophosphate salt.
- As result of extensive research and experimentation it has suprisingly been found now that improved thickened aqueous single phase cleaning compositions could be obtained, which comprise:
- a. from 0.1% to 10% by weight of a surfactant selected from the group consisting of (1) quaternary ammonium compounds wherein at least one of the hydrocarbon groups linked to nitrogen is a linear or branched alkyl or unsaturated hydrocarbon group containing at least 12 carbon atoms and preferably 16-20 carbon atoms and wherein two or three of the groups linked to the nitrogen are independently optionally substituted alkyl groups which contain 1 to 6 carbon atoms and wherein one or more of the alkyl groups may contain an aryl substituent or may be replaced by an aryl group and wherein an anion is present such as halide, acetate, methosulphate and the like, and (2) tertiary amine oxides wherein at least one of the hydrocarbon groups linked to nitrogen is a linear or a branched alkyl or unsaturated hydrocarbon group containing at least 16 carbon atoms and preferably 16-20 carbon atoms and wherein two of the groups linked to the nitrogen are independently optionally substituted alkyl groups which contain 1-6 carbon atoms and wherein one or more of the alkyl groups may contain an aryl substituent or may be replaced by an aryl group.
- b from 0.01 % up to 3% by weight of an organic anionic sulphonate selected from the group consisting of cumene sulphonate, xylene sulphonate, and toluene sulphonate in their acid or salt form and mixtures thereof, and
- c. water, wherein optionally one or more cleaning, desinfecting and/or odorizing agents are dissolved or dispersed, the percentage by weight being calculated on the weight of the total aqueous composition.
- Examples of such cleaning, desinfecting and/or odorizing agents are auxiliary detergents, acids, detergent builder salts, perfumes, antibiotics or active chlorine providing means.
- A preferred embodiment of the present invention is formed by thickened aqueous cleaning compositions having a pH of not more than 7 and preferably between 0 and 6 and more preferably between 0-4, and containing 1-15% by weight of an acid, normally occurring in cleaning compositions.
- Typical examples of quaternary ammonium compounds referred to under (a) are:
- ethyl-dimethyl-stearyl ammonium chloride,
- ethyl-dimethyl-stearyl ammonium bromide
- cocoalkyl-trimethyl ammonium chloride,
- hydrogenated tallow-trimethyl ammonium chloride,
- hydrogenated tallow-trimethyl ammonium bromide
- stearyl-trimethyl ammonium chloride,
- stearyl-trimethyl ammonium bromide,
- trimethyl-cetyl ammonium bromide,
- dimethyl-ethyl-lauryl ammonium chloride,
- tallow trimethyl ammonium chloride,
- tallow trimethyl ammonium bromide,
- and the corresponding methosulphates, acetates, and the like.
- A preferred group of the cationic ammonium compounds are:
- (hydrogenated) tallow-trimethyl ammonium chloride,
- (hydrogenated) tallow-trimethyl ammonium bromide,
- tallow trimethyl ammonium bromide,
- tallow trimethyl ammonium chloride,
- soja alkyl-trimethyl ammonium chloride,
- soja alkyl-trimethyl ammonium bromide,
- cetyl-trimethyl ammonium chloride, and
- methyl-bis(2-hydroxy ethyl)oleyl ammonium chloride.
- Most preferably tallow-trimethyl ammonium chloride is used.
- Typical examples of tertiary amine oxides referred to under (a) are:
- bis(2-hydroxy ethyl) cetylamine oxide,
- bis(2-hydroxy ethyl) tallowamine oxide,
- bis(2-hydroxy ethyl) hydrogenated tallow amine oxide,
- bis(2-hydroxy ethyl) stearylamine oxide,
- bis(2-hydroxy propyl) tallowamine oxide,
- bis(2-hydroxy propyl) stearyl amine oxide,
- dimethyl tallowamine oxide,
- dimethyl cetylamine oxide,
- dimethyl stearylamine oxide, and
- di-ethyl stearylamine oxide.
- A preferred group of the amine oxides are:
- dimethyl cetylamine oxide, and
- bis(2-hydroxy ethyl) tallowamine oxide.
- Most preferably bis(2-hydroxy ethyl) tallowamine oxide is used.
- The amine oxide and/or quaternary ammonium compound may preferably be used in amounts from 0.1% to 5% by weight based on the total weight of the composition dependent on the viscosity and the type of the agent desired.
- A preferred embodiment of the present invention is formed by thickened compositions containing one or more salts of the specified sulphonates. Typical salts of the sulphonates specified under (b) are the sodium, potassium, ammonium, lower amine and alkanolamine salts, of which the sodium salts are preferred.
- Typical acids which may be applied in the compositions of the present invention are sulphuric acid, phosphoric acid, sulphamic acid, hydrochloric acid, citric acid, acetic acid, formic acid or an acidic salt of the type conventionally used in cleaning compositions, or combinations thereof in an amount of from 1-15%.
- More preferably, citric acid or hydrochloric acid should be used in an amount from 1-10% by weight, based on the total composition.
- The compositions according to the present invention exhibit a viscosity of at least 200 m.Pa.s at 20 ° C.
- For compositions exhibiting optimum thickening effects, the ratio of the weights of the quaternary ammonium compound or tertiary amine oxide to the sulphonate is in the range from 0.1-6 and preferably from 1.5-2.5 and more preferably around about 2.0.
-
- The thickening systems described above display a viscosity temperature relationship that has a parabolic profile with the maximum viscosity being exhibited at a temperature in the range from 0 ° C to 30 °C. An increase in chain length of higher alkyl chain in the quaternary ammonium ion or amine oxide in general increases the temperature at which this peak occurs while a reduction in this higher alkyl chain length and/or branching in this alkyl group, reduces the temperature at which the maximum viscosity is produced by the system.
- It will be appreciated by persons skilled in the art that the ideal situation, wherein the viscosity of the composition should be independent of temperature over a temperature range which encompasses the practical domestic use conditions, i.e., from 5°-25°C, is approached most closely by the compositions of the present invention, employing a blend of surfactants and specific sulphonate(s), the application of which would certainly be rejected by persons skilled in the art.
- It will be appreciated by persons skilled in the art that the optimal characteristics of the compositions of the present invention will be governed by the specific kind of surfactant (quaternary ammonium ion or amine oxide), kind of sulphonate, kind of acid in the composition, amount of acid electrolyte concentration in total composition, ratio of weights of the surfactant-sulphonate combinations, and counter ion of the sulphonates.
The thickening compositions according to the present invention have however appeared to be rather insensitive to other types of ingredients occurring in the complete aqueous cleaning composition, such as perfume. - For example, for optimal results, the weight ratio of tallow trimethyl ammonium chloride and sodium xylene sulphonate in citric acid solution of 4.5% by weight (100%), i.e., 5% of hydrated citric acid, may vary from 2.0-2.5, and more preferably 2.15-2.25, while acceptable compositions for practical purposes may show ratios from 0.5-4.0 (based on 100% ingredients).
- It will be appreciated that another feature of the invention is formed by the use of a thickening premix composition, which comprises at least:
- a) a surfactant selected from the group consisting of quaternary ammonium compounds and tertiary amine oxides as defined hereinbefore, and
- b) an organic, anionic sulphonate selected from the group consisting of cumene sulphonate, xylene sulphonate, and toluene sulphonate, in their acid or salt form, and mixtures thereof, in a weight ratio of both ingredients as indicated before,
for the preparation of the thickened aqueous single-phase cleaning compositions. - The application of such thickening premix compositions has appeared to be rather insensitive to the presence of other ingredients in the final cleaning composition, e.g., perfume.
Such thickening premix compositions have been found to consist of homogeneous mixtures of components (a) and (b) and to exhibit a long storage stability. When mixed with water or an aqueous solution they display a surprising thickening effect. - Another feature of the present invention is formed by the application of the thickened aqueous single phase compositions according to the usual methods of this specific art of cleaning non-horizontal surfaces such as walls, windows and sanitary fittings.
- The invention is illustrated by the following examples but not with the intention to restrict its scope to these embodiments.
- Preparation of thickened cleaning composition comprising xylene sulphonate and tallow trimethyl ammonium chloride.
- Citric acid monohydrate (5.0 g) is dissolved in about 85.0 ml of demineralized water, with stirring, at 20 ° C, whereafter 2.2 g of tallow trimethyl ammonium chloride (as 50% solution Arquad T 50@) are added, followed by the addition of 1.25 g of sodium xylene sulphonate (as 40% solution), with continued stirring. The viscosity increases immediately during the addition of the sulphonate. After addition, with stirring, of 0.001 g of Acidol Blau BE/NW@ dye previously dissolved in 6.5 ml of demineralized water and 0.1 g of Floral Rose@ Perfume, stirring is continued until the perfume is completely dispersed (about 1-15 min., dependent on the type of applied perfume).
- To facilitate dispersion of the perfume in the finished composition the perfume may be mixed with the tallow trimethyl ammonium chloride.
- The obtained composition comprises:
- 2.2 % by weight of tallow trimethyl ammonium chloride (50%)
- 1.25 % by weight of sodium xylene sulphonate (40%)
- 5.0 % by weight of hydrated citric acid
- 0.001 % by weight of dye (Acidol Blue BE/NW)
- 0.1 % of perfume
- and water to 100%.
- The composition shows a good viscosity and is completely clear and stable at elevated temperature (40 °C). The colour does not change during storage.
- The viscosity was measured by Brookfield LVT, 60 rev/min, 230 m Pa.s (20°C). The composition did not show any cloud point on cooling down to 0 °C, and on heating up to 95 °C.
-
- The viscosities were measured by using a Brookfield LVT 60 rpm.
-
- All indicated percentages are by weight, based on the weight of the total composition.
- As to the addition of perfume to both compositions, composition I was reported as becoming cloudy and thin, while composition II remained clear and had a viscosity of 190 m Pa.s. at 20 °C. The same behaviour could be observed in the case of similar compositions containing sodium cumene sulphonate or sodium toluene sulphonate, showing a rather small perfume susceptibility which permits the use of premix compositions derived from sulphonate-quaternary ammonium derivatives.
- Whereas composition I did not show significant thickening effects in, e.g., 10% HCI and 5% H2S04, composition II could be applied in all acids specified in Example 2.
- Compositions were prepared along the lines of the process described in Example 1, starting from bis(2-hydroxy ethyl) tallowamine oxide (Aromox T12@) in amounts from 3 to 7% by weight,
sodium xylene sulphonate, sodium toluene sulphonate, sodium cumene sulphonate, or secondary n-alkane sulphonates of the formulae - Comparison of the viscosity values at 20°C of above prepared aqueous compositions containing varying amounts of the amine oxides (from 3 7% by weight) clearly showed that combination I, consisting of amine oxide and sodium salts of xylene sulphonate, toluene sulphonate, or cumene sulphonate, exhibited significantly better thickening characteristics than combination II consisting of amine oxide and n-alkane sulphonate (according to relevant prior art).
- Moreover, the thickening properties of compositions containing amine oxide and olefin sulphonates (e.g. ELFAN OS46@) III showed inferior thickening properties as compared with combination I and moreover had an intensive yellow colour.
- Among the tested compositions the amine oxide (Aromox T12@) and sodium xylene sulphonate showed the most attractive characteristics.
Claims (11)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT87201850T ATE103970T1 (en) | 1986-09-29 | 1987-09-26 | THICKENED WATER CLEANING AGENTS. |
EP87201850A EP0265979B2 (en) | 1986-09-29 | 1987-09-26 | Thickened aqueous cleaning compositions |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP86201667 | 1986-09-29 | ||
EP86201667 | 1986-09-29 | ||
EP87201850A EP0265979B2 (en) | 1986-09-29 | 1987-09-26 | Thickened aqueous cleaning compositions |
Publications (4)
Publication Number | Publication Date |
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EP0265979A2 EP0265979A2 (en) | 1988-05-04 |
EP0265979A3 EP0265979A3 (en) | 1989-08-16 |
EP0265979B1 true EP0265979B1 (en) | 1994-04-06 |
EP0265979B2 EP0265979B2 (en) | 1998-06-03 |
Family
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EP87201850A Expired - Lifetime EP0265979B2 (en) | 1986-09-29 | 1987-09-26 | Thickened aqueous cleaning compositions |
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AT (1) | ATE103970T1 (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
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US5336426A (en) * | 1987-11-17 | 1994-08-09 | Rader James E | Phase stable viscoelastic cleaning compositions |
US5055219A (en) * | 1987-11-17 | 1991-10-08 | The Clorox Company | Viscoelastic cleaning compositions and methods of use therefor |
TR27379A (en) * | 1992-07-29 | 1995-02-01 | Clorox Co | Phase balanced viscoelastic cleaning compositions. |
US5399285A (en) * | 1992-10-30 | 1995-03-21 | Diversey Corporation | Non-chlorinated low alkalinity high retention cleaners |
GB2273721B (en) * | 1992-12-24 | 1996-05-01 | Jeyes Group Plc | Bleaches |
CA2107939C (en) * | 1993-01-13 | 2001-01-30 | Stephen B. Kong | Acidic aqueous cleaning compositions |
US5977054A (en) * | 1993-09-01 | 1999-11-02 | The Procter & Gamble Company | Mildly acidic hard surface cleaning compositions containing amine oxide detergent surfactants |
DE69413991T2 (en) * | 1993-09-01 | 1999-06-02 | The Procter & Gamble Co., Cincinnati, Ohio | METHOD FOR CLEANING VINYL SURFACES USING LOW ACID CLEANING AGENTS FOR HARD SURFACES WITH AMINOXIDE TENIDE |
EP0790296B1 (en) * | 1993-11-29 | 2000-09-06 | The Procter & Gamble Company | Limescale removal compositions |
CA2191135C (en) * | 1994-05-31 | 2000-01-18 | Neil James Gordon | Cleaning compositions |
ES2189834T3 (en) * | 1994-11-25 | 2003-07-16 | Procter & Gamble | THICKENED COLORING COMPOSITIONS, METHOD OF USE AND PROCEDURE TO MANUFACTURE THEM. |
EP0726309B1 (en) * | 1995-02-08 | 2001-12-12 | The Procter & Gamble Company | Limescale removal compositions |
ES2236072T3 (en) * | 1995-02-08 | 2005-07-16 | THE PROCTER & GAMBLE COMPANY | COMPOSITIONS FOR THE ELIMINATION OF CAL INCRUSTATIONS. |
DE19504192A1 (en) * | 1995-02-09 | 1996-08-14 | Henkel Ecolab Gmbh & Co Ohg | Thickening aqueous cleaning agents for hard surfaces |
NL1000065C2 (en) * | 1995-04-05 | 1996-10-08 | Dija Zeist B V | Method and means for cleaning surfaces. |
EP0745663A1 (en) | 1995-05-31 | 1996-12-04 | The Procter & Gamble Company | Colored acidic aqueous liquid compositions comprising a peroxy-bleach |
DE19731398A1 (en) | 1997-07-22 | 1999-01-28 | Henkel Ecolab Gmbh & Co Ohg | Use of enzyme-containing solutions for cleaning fermentation and storage tanks |
DE19918188A1 (en) | 1999-04-22 | 2000-10-26 | Cognis Deutschland Gmbh | Cleaning agent, especially for cleaning toilet bowls, is typically in form of high foaming viscous gel and includes ethoxylated fatty amine as a thickener |
DE19918183A1 (en) * | 1999-04-22 | 2000-10-26 | Cognis Deutschland Gmbh | Cleaning agent for hard surfaces, typically in the form of a high foaming viscous gel, includes a combination of cationic surfactants, oligoglycosides and sulf(on)ate surfactants |
GB2375356A (en) * | 2001-05-11 | 2002-11-13 | Reckitt Benckiser Nv | Cationic fabric softening compositions |
PT3008159T (en) | 2013-06-12 | 2017-02-10 | Unilever Nv | Pourable detergent composition comprising suspended particles |
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BE610313A (en) * | 1960-11-14 | |||
ZA674667B (en) * | 1966-08-11 | |||
GB1294642A (en) * | 1969-05-29 | 1972-11-01 | Colgate Palmolive Co | Fabric softening composition and process |
ZA732200B (en) * | 1972-05-04 | 1974-11-27 | Colgate Palmolive Co | Softener dispersion |
US3892669A (en) * | 1972-10-27 | 1975-07-01 | Lever Brothers Ltd | Clear fabric-softening composition |
DE2849225A1 (en) * | 1977-11-18 | 1979-05-23 | Unilever Nv | POURABLE, LIQUID BLEACHING AGENTS |
GB8312619D0 (en) * | 1983-05-07 | 1983-06-08 | Procter & Gamble | Surfactant compositions |
US4587030A (en) * | 1983-07-05 | 1986-05-06 | Economics Laboratory, Inc. | Foamable, acidic cleaning compositions |
GB8513293D0 (en) * | 1985-05-28 | 1985-07-03 | Procter & Gamble Ntc Ltd | Cleaning compositions |
-
1987
- 1987-09-26 AT AT87201850T patent/ATE103970T1/en not_active IP Right Cessation
- 1987-09-26 EP EP87201850A patent/EP0265979B2/en not_active Expired - Lifetime
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EP0265979A3 (en) | 1989-08-16 |
EP0265979A2 (en) | 1988-05-04 |
ATE103970T1 (en) | 1994-04-15 |
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