US3663445A - Surface cleaning and defatting composition - Google Patents
Surface cleaning and defatting composition Download PDFInfo
- Publication number
- US3663445A US3663445A US852478A US3663445DA US3663445A US 3663445 A US3663445 A US 3663445A US 852478 A US852478 A US 852478A US 3663445D A US3663445D A US 3663445DA US 3663445 A US3663445 A US 3663445A
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- United States
- Prior art keywords
- concentrates
- cleaning
- ethylene oxide
- compositions
- water
- Prior art date
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- 239000000203 mixture Substances 0.000 title abstract description 47
- 238000004140 cleaning Methods 0.000 title abstract description 37
- 239000012141 concentrate Substances 0.000 abstract description 35
- 150000004665 fatty acids Chemical class 0.000 abstract description 30
- 235000014113 dietary fatty acids Nutrition 0.000 abstract description 27
- 229930195729 fatty acid Natural products 0.000 abstract description 27
- 239000000194 fatty acid Substances 0.000 abstract description 27
- 239000012895 dilution Substances 0.000 abstract description 10
- 238000010790 dilution Methods 0.000 abstract description 10
- 239000007788 liquid Substances 0.000 abstract description 7
- 239000002736 nonionic surfactant Substances 0.000 abstract description 7
- 150000003839 salts Chemical class 0.000 abstract description 5
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 32
- 235000008504 concentrate Nutrition 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 23
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 11
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 11
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 229960004418 trolamine Drugs 0.000 description 9
- 239000007859 condensation product Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- 239000002184 metal Substances 0.000 description 8
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 238000003860 storage Methods 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- -1 greases Substances 0.000 description 6
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 150000002169 ethanolamines Chemical class 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000012224 working solution Substances 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 2
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000007514 bases Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000014666 liquid concentrate Nutrition 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000004071 soot Substances 0.000 description 2
- 229940087291 tridecyl alcohol Drugs 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 125000005521 carbonamide group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002780 morpholines Chemical class 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 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
- C11D10/00—Compositions of detergents, not provided for by one single preceding group
- C11D10/04—Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
-
- 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
- C11D1/72—Ethers of polyoxyalkylene glycols
-
- 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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/30—Amines; Substituted amines ; Quaternized amines
-
- 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
- C11D1/02—Anionic compounds
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/06—Ether- or thioether carboxylic acids
-
- 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
- C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
- C11D1/521—Carboxylic amides (R1-CO-NR2R3), where R1, R2 and R3 are alkyl or alkenyl groups
Definitions
- the present invention relates to surface-cleaning and defatting compositions, particularly for metal surfaces. They should be free from strong alkali and above all they should be capable of being prepared from a liquid storable concentrate by simple dilution with water.
- compositions of the invention have the advantage that they can be built up exclusively on an aqueous basis, i.e., free from organic solvents, which is particularly advantageous in cases in which a very active and yet mild defatting and cleaning composition is required, which must be free from organic solvents in view of waste water problems, fire and explosion risks, etc. It is also possible, however, to incorporate organic solvents, in particular hydrocarbons, into them, up to about 50% of the total mixture, the product being a clear, homogeneous solution which is miscible under all conditions and in any ratio with water.
- compositions in question should be suitable for use in cleaning equipment, such as for instance immersion baths, flooding baths and spraying apparatus, in ultrasonic and steam jet equipment, in screening and centrifugal drums, as well as for the cleaning of objects and equipment by hand.
- cleaning equipment such as for instance immersion baths, flooding baths and spraying apparatus, in ultrasonic and steam jet equipment, in screening and centrifugal drums, as well as for the cleaning of objects and equipment by hand.
- the cleaning compositions should be deliverable in as concentrated a liquid form as possible, for economy of transport and packaging and so as to permit the preparation of the working solutions by simple dilution, without loss of time in dissolving solid components.
- the concentrates must not separate out or change during storage. They should also remain stable in the face of fluctuations in temperature.
- the invention relates to cleaning and defatting compositions which particularly in this respect fulfill the needs of technical practice better than those known to date, and which are distinguished both by an excellent cleaning effect and--in the form of liquid concentratesby particularly good storage properties.
- these concentrates are non-toxic; their solutions are non-corrosive, can be used without risk for manual cleaning and do not develop toxic or inflammable vapors, either in the cold or on heating. Spent solutions do not require any additional treatment before being discharged into the drainage systems.
- the cleaning compositions according to the invention can be prepared from liquid concentrates by dilution with water and are characterized in that these concentrates are prepared from three active components in specific quantitative proportions. These active components are the following:
- the ultimate concentrates and cleaning compositions contain the nonionic surfactant, the alkanolamine and the alkanolamine salt or soap of the fatty acid due to the reaction between the fatty acid and an excess of the alkanolamine under the mild temperature conditions used for preparing the concentrates.
- the fatty acids used in preparing the concentrates should amount to at least 3% by weight, the nonionic surface-active condensation products should be used in at least double the amount of the fatty acids, and the alkanolamines used in at least 1.5-fold or preferably 3- fold molar excess with respect to the fatty acids, that 15, at least 2.5 moles or preferably 4 moles alkanolamine per mole fatty acid.
- the amount of fatty acid used in preparing the concentrates lies between approximately 3.5% and 15% by weight, the amount of nonionic surface-active substances used is about 20% to 45% by weight, and the molar ratio fatty acid; alkanolamine lies between 1:6 and 1:20.
- the working solutions for cleaning and defatting use can be prepared from the concentrates by dilution with water in a concentrate to water ratio of 1: 10 to 1:200, preferably of 1:25 (parts by weight). In this connection no special demands are to be made upon the quality of the water.
- the water content in the solutions ready for cleaning and defatting use amounts to 91-99.75% by weight.
- the nonionic ethylene oxide condensation products to be used in the liquid cleaning and defatting agents can be prepared in the conventional way by the addition of about 3-15 moles ethylene oxide to a basic compound containing active hydrogen.
- Such basic compounds may include substances containing hydroxylic, carboxylic and carbonamide groups.
- nonionic addition products there can be used, for instance, the adducts of about 3-15 moles ethylene oxide to oxygen-containing compounds, such as alkyl phenols with 1-3 alkyl substituents, in which the sum of the carbon atoms of the alkyl radicals amounts to about 6-20, or primary, secondary or tertiary alcohols with 8-22 carbon atoms, or organic carboxylic acids with 8-22 carbon atoms.
- Nonionic surfactants of the above types are further described in US. Pats. Nos. 1,970,578 to Schoeller et al., 2,174,761 to Schuette et al. and 2,213,477 to Steindorlf et al., the disclosures of which compounds are incorporated by reference herein.
- nonionic, surface-active addition products those substances are preferred which effect a particularly strong decrease in the surface-tension of the water, which have a good wetting effect and which are particularly capable of emulsifying fats, oils and waxes.
- Suitable products are, for instance, the addition products of 3-15 moles ethylene oxide with alkyl phenols, alcohols and fatty acid amides.
- ethoxylated alkyl phenols are used with about 3-9 ethylene oxide moles per base molecule, in particular mixtures of nonyl phenols with about 5-6 and nonyl phenols with about 8-9 ethylene oxide moles.
- Very useful mixtures are also those consisting of a nonyl phenol condensed with 6 moles of ethylene oxide and a tridecyl alcohol condensed with about 15 moles of ethylene oxide.
- mixtures of nonionic substances instead of a single substance in the compositions of the invention gives the advantage of a particularly broad range of action with respect to all kinds of soiling, together with a further increase in the storage stability of the concentrates. It is advantageous if the nonionic component with the shorter alkylene oxide chain is present in the mixture in predominant amount, i.e., exceeds the amount of the nonionic component with the longer alkylene oxide chain.
- the fatty acid reactant to be used in preparing the concentrate may be saturated or unsaturated and contain 8-22 carbon atoms in the molecule, preferably 12-18 carbon atoms. It may be recovered from, for instance, natural fats of vegetable or animal origin. It is advantageous to use the more strongly hydrotropically-active long-chain fatty acids with 16-18 carbon atoms. Representative examples thereof include caprylic, capric, lauric, myristic, palmitic, stearic, arachidic, behenic, oleic, palmitoleic, linoleic, linolenic and elaeostearic acids. Mixtures containing oleic acid and, in particular, oleic acid itself are preferred.
- Particularly suitable as alkanolamines are short chain alkanolamines, for instance, mono-, diand triethanolamines, which may be used alone or in admixture.
- compositions prepared from nonionics, fatty acid and alkanolamines have an excellent cleaning and defatting effect, if the three components mentioned are employed in the ratios according to the invention.
- the cleaning and defatting effect is considerably greater than could be expected on the ground of the separate components present in the final compositions.
- additives commonly used in the cleaning of metals can be incorporated, such as rust inhibitors, water softening agents, passivization agents, for improving the soil-suspending power, etc.
- compositions for preparing a few concentrates according to the invention will now be given below by way of example:
- the alkanolamine component reacts in the classical process with the fatty acid component to form the alkanolamine salt or soap of the fatty acid and to leave unreacted excess alkanolamine in the final concentrates. Therefore, the final concentrates contain from about 6% to about 45% by weight of the nonionic surfactant, from about 4% to about 33% by weight of the alkanolamine salt of the fatty acid, from about 2% to about 90% by weight of the alkanolamine and from about to about 50% by weight of water.
- EXAMPLE 6 This example, prepared as above, is included to show that compositions which contain the above three essential ingredients but in which the conditions according to the invention are not fulfilled have unsatisfactory storability performance.
- compositions prepared as above, were also found to be unsatisfactory in storage stability and/ or cleaning ability.
- the content of nonionic is too low.
- compositions prepared as above, were also found to be unsatisfactory in storage stability and/ or cleaning ability.
- the content of fatty acid is too low.
- a nonionic surface active condensation product of about 3-15 moles of ethylene oxide with a basic organic compound selected from the class consisting 6 of alkyl phenols having a total of 6' to 20 alkyl carbon atoms, C to C alcohols, C to C carboxylic acids and C to C amides;
- the amount by weight of nonionic surface active condensation product is at least double the amount of the fatty acid moiety of the ethanolamine salt
- the molar ratio of the free ethanolamine to the fatty acid moiety of the ethanolamine salt is at least 1.5 :1
- the fatty acid moiety of the ethanolamine salt of a fatty acid is at least 3% by weight of the total composition.
- nonionic surface active condensation product is a mixture of a condensate of nonyl phenol with about 56 moles of ethylene oxide and a condensate of nonyl phenol with about 89 moles of ethylene oxide, the condensate with the shorter ethylene oxide chain being present in a predominant amount of said mixture of nonionic surfactants.
- nonionic surface active condensation product is a mixture of a condensate of tridecyl alcohol with about 15 moles of ethylene oxide and a condensate of nonylphenol with about 6 moles of ethylene oxide, the condensate with the shorter ethylene oxide chain being present in a predominant amount of said mixture of nonionic surfactants.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
LIQUID STORABLE CONCENTRATES AND CLEANING AND DEFATTING COMPOSITIONS, PARTICULARLY FOR METAL SURFACES, PREPARED FROM SAID CONCENTRATES BY DILUTION WITH WATER, WHEREIN THE CONCENTRATES COMPRISE A NONIONIC SURFACTANT, AN ALKANOLAMINE SALT OF A FATTY ACID AND AN ALKALOLAMINE.
Description
United States Patent 3,663,445 SURFACE CLEANING AND DEFATTING COMPOSITION Horst Augustin and Siegfried Klussendorf, Mannheim,
Germany, and Konrad Kofer, Vienna, Austria, assignors to Lever Brothers Company, New York, N.Y. No Drawing. Continuation-impart of application Ser. No. 805,966, Feb. 24, 1969, which is a continuation-in-part of application Ser. No. 537,282, Mar. 25, 1966. This application Aug. 22, 1969, Ser. No. 852,478
Int. Cl. Clld 9/30 U.S. Cl. 252-117 6 Claims ABSTRACT OF THE DISCLOSURE Liquid storable concentrates and cleaning and defatting compositions, particularly for metal surfaces, prepared from said concentrates by dilution with water, wherein the concentrates comprise a nonionic surfactant, an alkanolamine salt of a fatty acid and an alkalolamine.
This application is a continuation-in-part of our copending U.S. application Ser. No. 805,966, filed Feb. 24, 1969 (now abandoned), which in turn is a continuationin-part of our U.S. application Ser. No. 537,282, filed Mar. 25, 1966 (now abandoned).
The present invention relates to surface-cleaning and defatting compositions, particularly for metal surfaces. They should be free from strong alkali and above all they should be capable of being prepared from a liquid storable concentrate by simple dilution with water.
The compositions of the invention have the advantage that they can be built up exclusively on an aqueous basis, i.e., free from organic solvents, which is particularly advantageous in cases in which a very active and yet mild defatting and cleaning composition is required, which must be free from organic solvents in view of waste water problems, fire and explosion risks, etc. It is also possible, however, to incorporate organic solvents, in particular hydrocarbons, into them, up to about 50% of the total mixture, the product being a clear, homogeneous solution which is miscible under all conditions and in any ratio with water. This results in such an improvement of the cleaning effect as to permit even the removal of combustion residues, such as oil soot, coal soot and other cracking products, which up to now could only be removed with highly toxic cleaning agents, such as phenols or chlorinated hydrocarbons.
There is a considerable interest in many branches of industry in such fully preformulated cleaning and defatting compositions, which after dilution with water remove soiling of an organic or inorganic nature from metal or plastic objects, equipment, machinery and tools, and which can also be used for the corresponding pretreatment of metal surface before these are subjected to certain processes. The industries referred to include, for instance, the metalworking, galvanic, engineening, light engineering and motor industries, as well as the radio gramophone and optical industries. The compositions in question should also fulfill the requirement that they are simple for less skilled workmen to use. They should permit the removal of metal .bore chips, polishing paste and other polishing agents, greases, lubricating oils, plastic particles, sand, traces of hand perspiration and other contaminations without in any way damaging metal surfaces or any lacquer or plastic coating present.
The compositions in question should be suitable for use in cleaning equipment, such as for instance immersion baths, flooding baths and spraying apparatus, in ultrasonic and steam jet equipment, in screening and centrifugal drums, as well as for the cleaning of objects and equipment by hand.
In view of their universal applicability, such cleaning and defatting compositions should be fully effective at high and low solution temperatures; they must not have a corrosive eifect and should be physiologically unobjectionable. When the working solution is heated, neither toxic nor inflammable vapors should develop. Also in industry no problems should arise with respect to the disposal of waste water when the compositions are used on a large scale.
Moreover, the cleaning compositions should be deliverable in as concentrated a liquid form as possible, for economy of transport and packaging and so as to permit the preparation of the working solutions by simple dilution, without loss of time in dissolving solid components. The concentrates must not separate out or change during storage. They should also remain stable in the face of fluctuations in temperature.
It will be evident that it is not easy to meet these many demands in one product. Difficulties particularly arise in reconciling the requirements as to cleaning and defatting efficiency with the requirements that the working solution should be capable of being prepared by simple dilution with water of liquid concentrates and these concentrates should have good storage properties in the face of fluctuations of temperature.
The invention relates to cleaning and defatting compositions which particularly in this respect fulfill the needs of technical practice better than those known to date, and which are distinguished both by an excellent cleaning effect and--in the form of liquid concentratesby particularly good storage properties. In addition, these concentrates are non-toxic; their solutions are non-corrosive, can be used without risk for manual cleaning and do not develop toxic or inflammable vapors, either in the cold or on heating. Spent solutions do not require any additional treatment before being discharged into the drainage systems.
The cleaning compositions according to the invention can be prepared from liquid concentrates by dilution with water and are characterized in that these concentrates are prepared from three active components in specific quantitative proportions. These active components are the following:
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(a) nonionic surface-active condensation products of about 3-15 moles ethylene oxide with an organic compound containing an active hydrogen bound to oxygen or nitrogen atoms;
(b) fatty acids;
(c) alkanolamines.
As explained hereinafter the ultimate concentrates and cleaning compositions contain the nonionic surfactant, the alkanolamine and the alkanolamine salt or soap of the fatty acid due to the reaction between the fatty acid and an excess of the alkanolamine under the mild temperature conditions used for preparing the concentrates.
The fatty acids used in preparing the concentrates should amount to at least 3% by weight, the nonionic surface-active condensation products should be used in at least double the amount of the fatty acids, and the alkanolamines used in at least 1.5-fold or preferably 3- fold molar excess with respect to the fatty acids, that 15, at least 2.5 moles or preferably 4 moles alkanolamine per mole fatty acid.
In the preferred embodiments of the invention, particularly if the compositions are to be free from organic solvents, the amount of fatty acid used in preparing the concentrates lies between approximately 3.5% and 15% by weight, the amount of nonionic surface-active substances used is about 20% to 45% by weight, and the molar ratio fatty acid; alkanolamine lies between 1:6 and 1:20. As far as the concentrates contain water, this should amount up to 50% by weight. The working solutions for cleaning and defatting use can be prepared from the concentrates by dilution with water in a concentrate to water ratio of 1: 10 to 1:200, preferably of 1:25 (parts by weight). In this connection no special demands are to be made upon the quality of the water. Corresponding to these dilution ratios, the water content in the solutions ready for cleaning and defatting use amounts to 91-99.75% by weight.
The nonionic ethylene oxide condensation products to be used in the liquid cleaning and defatting agents can be prepared in the conventional way by the addition of about 3-15 moles ethylene oxide to a basic compound containing active hydrogen. Such basic compounds may include substances containing hydroxylic, carboxylic and carbonamide groups. As nonionic addition products there can be used, for instance, the adducts of about 3-15 moles ethylene oxide to oxygen-containing compounds, such as alkyl phenols with 1-3 alkyl substituents, in which the sum of the carbon atoms of the alkyl radicals amounts to about 6-20, or primary, secondary or tertiary alcohols with 8-22 carbon atoms, or organic carboxylic acids with 8-22 carbon atoms. Also suitable are the corresponding addition products to nitrogen-containing compounds, such as carboxylic acid amides with 8-22 carbon atoms. Nonionic surfactants of the above types are further described in US. Pats. Nos. 1,970,578 to Schoeller et al., 2,174,761 to Schuette et al. and 2,213,477 to Steindorlf et al., the disclosures of which compounds are incorporated by reference herein.
Of the above-mentioned nonionic, surface-active addition products those substances are preferred which effect a particularly strong decrease in the surface-tension of the water, which have a good wetting effect and which are particularly capable of emulsifying fats, oils and waxes. Suitable products are, for instance, the addition products of 3-15 moles ethylene oxide with alkyl phenols, alcohols and fatty acid amides.
According to the invention, in compositions which, as concentrates, possess particularly good storage properties, combined with an excellent cleaning effect in the form of their diluted aqueous solutions, ethoxylated alkyl phenols are used with about 3-9 ethylene oxide moles per base molecule, in particular mixtures of nonyl phenols with about 5-6 and nonyl phenols with about 8-9 ethylene oxide moles. Very useful mixtures are also those consisting of a nonyl phenol condensed with 6 moles of ethylene oxide and a tridecyl alcohol condensed with about 15 moles of ethylene oxide. The use of mixtures of nonionic substances instead of a single substance in the compositions of the invention gives the advantage of a particularly broad range of action with respect to all kinds of soiling, together with a further increase in the storage stability of the concentrates. It is advantageous if the nonionic component with the shorter alkylene oxide chain is present in the mixture in predominant amount, i.e., exceeds the amount of the nonionic component with the longer alkylene oxide chain.
The fatty acid reactant to be used in preparing the concentrate may be saturated or unsaturated and contain 8-22 carbon atoms in the molecule, preferably 12-18 carbon atoms. It may be recovered from, for instance, natural fats of vegetable or animal origin. It is advantageous to use the more strongly hydrotropically-active long-chain fatty acids with 16-18 carbon atoms. Representative examples thereof include caprylic, capric, lauric, myristic, palmitic, stearic, arachidic, behenic, oleic, palmitoleic, linoleic, linolenic and elaeostearic acids. Mixtures containing oleic acid and, in particular, oleic acid itself are preferred.
"Particularly suitable as alkanolamines are short chain alkanolamines, for instance, mono-, diand triethanolamines, which may be used alone or in admixture.
It has surprisingly been found that the compositions prepared from nonionics, fatty acid and alkanolamines have an excellent cleaning and defatting effect, if the three components mentioned are employed in the ratios according to the invention. The cleaning and defatting effect is considerably greater than could be expected on the ground of the separate components present in the final compositions. In this connection it is essential that the composition be prepared from a high amount of nonionic surface-active substances and that the alkanolamines are used in a considerable excess in relation to the fatty acid. Only then also is the required storability of the concentrates obtained.
With the aid of the combination according to the invention, however, it is also possible to introduce into a specific mixture organic solvents which are water-insoluble per se, such as e.g., paraflin oil, diesel oil, petroleum, and thus achieve a particularly improved cleaning effect. Such a cleaning composition permits the removal of combustion residues that are particularly difficult to remove, e.g., those from vehicle motor pistons, without the use of substances required up to now that are dangerous to health, such as phenols and cresols.
In the concentrates according to the invention and also in the cleaning solutions, if desired, additives commonly used in the cleaning of metals can be incorporated, such as rust inhibitors, water softening agents, passivization agents, for improving the soil-suspending power, etc.
The following compositions for preparing a few concentrates according to the invention will now be given below by way of example:
EXAMPLE 1 Percent Oleic acid 5 Nonyl phenol-6 moles ethylene oxide condensate 30 Triethanolamine 50 Sodium ethylene diamine tetraacetate 1.1 Water to 100%. Oleic acid:
Acid value-199-202 Iodine value--9l Titre4-6 EXAMPLE 2 Mixed oils fatty acid 3.5 Nonyl phenol-6 moles ethylene oxide condensate 21 Tridecyl alcohol-15 moles ethylene oxide condensate 7 Triethanolamine 26 Sodium ethylene diamine tetraacetate 1.35 Water to Mixed oils fatty acid 12-20 carbon atoms.
EXAMPLE 3 Oleic acid 8 Nonyl phenol-6 moles ethylene oxides condensate 20 Nonyl phenol-8 moles ethylene oxide condensate 14 Triethanolamine 25 Perfume 0.05 Water to 100%.
EXAMPLE 4 Oleic acid 5 Nonyl phenol-6 moles ethylene oxide condensate 12 Triethanolamine 15 Kerosene K 27 Citric acid 1.4 Water to 100%.
EXAMPLE 5 Oleic acid 5 Nonylphenol-S moles ethylene oxide condensate 10 Tallow fatty acid amide-11 moles ethylene oxide condensate 20 Triethanolamine 50 Water 15 The above concentrates according to the invention, were prepared by adding the required amount of alkanolamine to the fatty acid charge with stirring while the mixture was slowly heated to approximately 50 C. The heating was then stopped after which the other ingredients were incorporated with good mixing but without special precautions.
In view of the above procedure for preparing the concentrates of the invention, the alkanolamine component reacts in the classical process with the fatty acid component to form the alkanolamine salt or soap of the fatty acid and to leave unreacted excess alkanolamine in the final concentrates. Therefore, the final concentrates contain from about 6% to about 45% by weight of the nonionic surfactant, from about 4% to about 33% by weight of the alkanolamine salt of the fatty acid, from about 2% to about 90% by weight of the alkanolamine and from about to about 50% by weight of water.
EXAMPLE 6 This example, prepared as above, is included to show that compositions which contain the above three essential ingredients but in which the conditions according to the invention are not fulfilled have unsatisfactory storability performance.
Percent A B C Uleic acid 5 5 Triethanolamlne alkyl benzene sulfonate 10 1O Nonyl phenol-l0 moles ethylene oxide condensate 5 10 Nonyl phenol-6 moles ethylene oxide condensate 15 10 Trldecyl alcohol-15 moles ethylene oxide condensate 5 10 Triethanolamine 5 5 5 Isopropanol.. 10 10 Water To 100 These compositions were found to be unsatisfactory in storage stability and/or cleaning ability. The amount of triethanolamine is too low in proportion to the fatty acid present.
The following compositions, prepared as above, were also found to be unsatisfactory in storage stability and/ or cleaning ability. The content of nonionic is too low.
The following compositions, prepared as above, were also found to be unsatisfactory in storage stability and/ or cleaning ability. The content of fatty acid is too low.
Percent F G H J Olelc acid Nonyl phenol-3 moles ethylene oxide condensate Nonyl phenol-8 moles ethylene oxide condensate Nonyl phenol-6 moles ethylene oxide condensate 21 2t Nonyl phenol-15 moles ethylene oxide condensate 5 Trideeyl alcohol-15 moles ethylene oxide condensate 7 Trlethanolamine Isopropanol Water What is claimed is:
1. Liquid storable concentrates and cleaning and defatting compositions, particularly for metal surfaces, prepared from said concentrates by dilution with water, consisting essentially of:
(a) a nonionic surface active condensation product of about 3-15 moles of ethylene oxide with a basic organic compound selected from the class consisting 6 of alkyl phenols having a total of 6' to 20 alkyl carbon atoms, C to C alcohols, C to C carboxylic acids and C to C amides;
(b) the mono-, dior tri-ethanolamine salt of a fatty acid having from 8 to 22 carbon atoms;
(0) mono-, dior tri-ethanolamine; and
(d) from about 0% to about 50% by weight of water;
in which the amount by weight of nonionic surface active condensation product is at least double the amount of the fatty acid moiety of the ethanolamine salt, the molar ratio of the free ethanolamine to the fatty acid moiety of the ethanolamine salt is at least 1.5 :1 and the fatty acid moiety of the ethanolamine salt of a fatty acid is at least 3% by weight of the total composition.
2. Concentrates and cleaning compositions according to claim 1, which consist essentially of:
(a) from about 6% to about 45% by weight of the nonionic surface active condensation product;
(b) from about 4% to about 33% by weight of the ethanolamine salt;
(0) from about 2% to about by weight of the ethanolamine; and
(d) from about 0% to about 50% by weight of water.
3. Concentrates and cleaning compositions according to claim 1 wherein the nonionic surface active condensation product is a mixture of a condensate of nonyl phenol with about 56 moles of ethylene oxide and a condensate of nonyl phenol with about 89 moles of ethylene oxide, the condensate with the shorter ethylene oxide chain being present in a predominant amount of said mixture of nonionic surfactants.
4. Concentrates and cleaning compositions according to claim 1 wherein the nonionic surface active condensation product is a mixture of a condensate of tridecyl alcohol with about 15 moles of ethylene oxide and a condensate of nonylphenol with about 6 moles of ethylene oxide, the condensate with the shorter ethylene oxide chain being present in a predominant amount of said mixture of nonionic surfactants.
5. Concentrates and cleaning compositions according to claim 1 wherein said ethanolamine salt of a fatty acid is the triethanolamine salt of oleic acid and wherein the ethanolamine is triethanolamine.
6. Concentrates and cleaning compositions according to claim 1 which are free from organic solvents.
References Cited UNITED STATES PATENTS 2,466,632 4/ 1949 Borus 252-118 2,583,165 1/1952 Campbell 252-118 2,700,654 1/1955 Holman 252-118 2,831,815 4/1958 Klisch 252-152 3,156,655 11/1964 Bright 252-109 2,874,126 2/ 1959 Epstein et al 252-152 3,222,201 12/1965 Boyle et a1 252-152 3,213,028 10/1965 Wood 252-89 3,352,695 11/1967 Iaciofano 252-89 OTHER REFERENCES Rainey et al.: Nonionic Surface Active Agents, Article in Chemical and Engineering News, vol. 31, No. 44, Nov. 2, 1953, pp. 4521-4523.
McCutcheons Detergents and Emulsifiers, 1967 annual, p. 262.
Union Carbide, Alkanolamines and Morpholines, 1960, pp. 8-9.
Union Carbide, Emulsions and Detergents, 1961, pp. 7 0-71.
Bennett: The Chemical Formulary, vol. XIII, 1967.
HERBERT B. GUYNN, Primary Examiner US. Cl. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85247869A | 1969-08-22 | 1969-08-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3663445A true US3663445A (en) | 1972-05-16 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US852478A Expired - Lifetime US3663445A (en) | 1969-08-22 | 1969-08-22 | Surface cleaning and defatting composition |
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| US (1) | US3663445A (en) |
Cited By (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2170037A1 (en) * | 1972-01-31 | 1973-09-14 | Procter & Gamble | |
| FR2170036A1 (en) * | 1972-01-31 | 1973-09-14 | Procter & Gamble | |
| US3870647A (en) * | 1972-06-05 | 1975-03-11 | Seneca Chemicals Inc | Liquid cleaning agent |
| US3876563A (en) * | 1972-09-22 | 1975-04-08 | Procter & Gamble | Liquid detergent compositions |
| US3935130A (en) * | 1972-07-19 | 1976-01-27 | Kabushiki Kaisha Tsumura Juntendo | Detergent composition for cleaning bathtubs |
| US3970762A (en) * | 1971-01-28 | 1976-07-20 | Compagnie Francaise De Produits Industriels | Method of chemical peeling of fruits and vegetables with an alkanolamine |
| US3975294A (en) * | 1972-11-03 | 1976-08-17 | Rhone-Poulenc S.A. | Surface active composition |
| US4018696A (en) * | 1974-11-25 | 1977-04-19 | Berol Kemi Ab | Liquid detergent composition |
| US4053314A (en) * | 1974-08-09 | 1977-10-11 | Kabushiki Kaisha Bunshodo | Amine developer liquid for diazotype reproduction |
| US4079078A (en) * | 1974-06-21 | 1978-03-14 | The Procter & Gamble Company | Liquid detergent compositions |
| US4105592A (en) * | 1974-06-21 | 1978-08-08 | The Procter & Gamble Company | Liquid detergent compositions |
| FR2389672A1 (en) * | 1977-05-06 | 1978-12-01 | Unilever Nv | |
| US4133779A (en) * | 1975-01-06 | 1979-01-09 | The Procter & Gamble Company | Detergent composition containing semi-polar nonionic detergent and alkaline earth metal anionic detergent |
| US4212758A (en) * | 1978-10-20 | 1980-07-15 | Belkevich Petr I | Cleansing agents containing oleic acid, isopropanol and ethylacetate |
| EP0019315A1 (en) * | 1979-05-16 | 1980-11-26 | Procter & Gamble European Technical Center | Highly concentrated fatty acid containing liquid detergent compositions |
| US4284434A (en) * | 1977-03-24 | 1981-08-18 | Henkel Kommanditgesellschaft Auf Aktien | Process for spray cleaning of metal surfaces |
| US4397754A (en) * | 1980-09-27 | 1983-08-09 | Caligen Foam Limited | Personal cleaning products |
| US4486329A (en) * | 1983-10-17 | 1984-12-04 | Colgate-Palmolive Company | Liquid all-purpose cleaner |
| US4509989A (en) * | 1983-03-25 | 1985-04-09 | United States Steel Corporation | Cleaning method for removing sulfur containing deposits from coke oven gas lines |
| EP0189752A3 (en) * | 1985-01-19 | 1986-10-29 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Agent and process for stripping photoresist and stripping rests from semiconductor surfaces |
| EP0213554A3 (en) * | 1985-08-28 | 1988-09-14 | Henkel Kommanditgesellschaft Auf Aktien | Demulsifying cleaning agent retaining superficial humidity |
| US4954286A (en) * | 1988-04-14 | 1990-09-04 | Lever Brothers Company | Fabric pretreatment cleaning compositions |
| US4992212A (en) * | 1988-10-18 | 1991-02-12 | Lever Brothers Company, Division Of Conopco, Inc. | Alkaline light duty liquid detergents that are non-staining to aluminum |
| DE4001595A1 (en) * | 1990-01-20 | 1991-07-25 | Henkel Kgaa | DEMULGATING, POWDERFUL, OR LIQUID CLEANSING AGENTS AND THEIR USE |
| US5399202A (en) * | 1991-12-19 | 1995-03-21 | Hitachi, Ltd. | Resist-peeling liquid and process for peeling a resist using the same |
| US5770549A (en) * | 1996-03-18 | 1998-06-23 | Henkel Corporation | Surfactant blend for non-solvent hard surface cleaning |
| US6465404B2 (en) | 2000-03-21 | 2002-10-15 | Bbj Environmental Solutions, Inc. | Aqueous cleaning composition with controlled PH |
| RU2218385C1 (en) * | 2002-08-29 | 2003-12-10 | Закрытое акционерное общество "ЭКОХИММАШ" | Detergent-preserving fluid concentrate |
| US20080277621A1 (en) * | 2007-05-10 | 2008-11-13 | Macdonald John Gavin | Colorant neutralizer |
| US20080276379A1 (en) * | 2007-05-10 | 2008-11-13 | Macdonald John Gavin | Methods for discharging colorants |
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| US9161869B2 (en) | 2012-03-30 | 2015-10-20 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with decolorizing agents |
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-
1969
- 1969-08-22 US US852478A patent/US3663445A/en not_active Expired - Lifetime
Cited By (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3970762A (en) * | 1971-01-28 | 1976-07-20 | Compagnie Francaise De Produits Industriels | Method of chemical peeling of fruits and vegetables with an alkanolamine |
| FR2170037A1 (en) * | 1972-01-31 | 1973-09-14 | Procter & Gamble | |
| FR2170036A1 (en) * | 1972-01-31 | 1973-09-14 | Procter & Gamble | |
| US3869399A (en) * | 1972-01-31 | 1975-03-04 | Procter & Gamble | Liquid detergent compositions |
| US3870647A (en) * | 1972-06-05 | 1975-03-11 | Seneca Chemicals Inc | Liquid cleaning agent |
| US3935130A (en) * | 1972-07-19 | 1976-01-27 | Kabushiki Kaisha Tsumura Juntendo | Detergent composition for cleaning bathtubs |
| US3876563A (en) * | 1972-09-22 | 1975-04-08 | Procter & Gamble | Liquid detergent compositions |
| US3975294A (en) * | 1972-11-03 | 1976-08-17 | Rhone-Poulenc S.A. | Surface active composition |
| US4079078A (en) * | 1974-06-21 | 1978-03-14 | The Procter & Gamble Company | Liquid detergent compositions |
| US4105592A (en) * | 1974-06-21 | 1978-08-08 | The Procter & Gamble Company | Liquid detergent compositions |
| US4053314A (en) * | 1974-08-09 | 1977-10-11 | Kabushiki Kaisha Bunshodo | Amine developer liquid for diazotype reproduction |
| US4018696A (en) * | 1974-11-25 | 1977-04-19 | Berol Kemi Ab | Liquid detergent composition |
| US4133779A (en) * | 1975-01-06 | 1979-01-09 | The Procter & Gamble Company | Detergent composition containing semi-polar nonionic detergent and alkaline earth metal anionic detergent |
| US4284434A (en) * | 1977-03-24 | 1981-08-18 | Henkel Kommanditgesellschaft Auf Aktien | Process for spray cleaning of metal surfaces |
| FR2389672A1 (en) * | 1977-05-06 | 1978-12-01 | Unilever Nv | |
| US4212758A (en) * | 1978-10-20 | 1980-07-15 | Belkevich Petr I | Cleansing agents containing oleic acid, isopropanol and ethylacetate |
| EP0019315A1 (en) * | 1979-05-16 | 1980-11-26 | Procter & Gamble European Technical Center | Highly concentrated fatty acid containing liquid detergent compositions |
| US4397754A (en) * | 1980-09-27 | 1983-08-09 | Caligen Foam Limited | Personal cleaning products |
| US4509989A (en) * | 1983-03-25 | 1985-04-09 | United States Steel Corporation | Cleaning method for removing sulfur containing deposits from coke oven gas lines |
| US4486329A (en) * | 1983-10-17 | 1984-12-04 | Colgate-Palmolive Company | Liquid all-purpose cleaner |
| EP0189752A3 (en) * | 1985-01-19 | 1986-10-29 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Agent and process for stripping photoresist and stripping rests from semiconductor surfaces |
| US4786578A (en) * | 1985-01-19 | 1988-11-22 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Agent and method for the removal of photoresist and stripper residues from semiconductor substrates |
| EP0213554A3 (en) * | 1985-08-28 | 1988-09-14 | Henkel Kommanditgesellschaft Auf Aktien | Demulsifying cleaning agent retaining superficial humidity |
| US4954286A (en) * | 1988-04-14 | 1990-09-04 | Lever Brothers Company | Fabric pretreatment cleaning compositions |
| US4992212A (en) * | 1988-10-18 | 1991-02-12 | Lever Brothers Company, Division Of Conopco, Inc. | Alkaline light duty liquid detergents that are non-staining to aluminum |
| DE4001595A1 (en) * | 1990-01-20 | 1991-07-25 | Henkel Kgaa | DEMULGATING, POWDERFUL, OR LIQUID CLEANSING AGENTS AND THEIR USE |
| US5399202A (en) * | 1991-12-19 | 1995-03-21 | Hitachi, Ltd. | Resist-peeling liquid and process for peeling a resist using the same |
| US5770549A (en) * | 1996-03-18 | 1998-06-23 | Henkel Corporation | Surfactant blend for non-solvent hard surface cleaning |
| US6465404B2 (en) | 2000-03-21 | 2002-10-15 | Bbj Environmental Solutions, Inc. | Aqueous cleaning composition with controlled PH |
| RU2218385C1 (en) * | 2002-08-29 | 2003-12-10 | Закрытое акционерное общество "ЭКОХИММАШ" | Detergent-preserving fluid concentrate |
| US20080276379A1 (en) * | 2007-05-10 | 2008-11-13 | Macdonald John Gavin | Methods for discharging colorants |
| US20080277621A1 (en) * | 2007-05-10 | 2008-11-13 | Macdonald John Gavin | Colorant neutralizer |
| AU2008249735B2 (en) * | 2007-05-10 | 2013-10-03 | Kimberly-Clark Worldwide, Inc. | Methods for discharging colorants |
| US9657257B2 (en) | 2007-05-10 | 2017-05-23 | Kimberly-Clark Worldwide, Inc. | Colorant neutralizer |
| US20090062764A1 (en) * | 2007-08-30 | 2009-03-05 | Kimberly-Clark Worldwide, Inc. | Zoned application of decolorizing composition for use in absorbent articles |
| US8815791B2 (en) | 2008-12-02 | 2014-08-26 | Diversey, Inc. | Cleaning of a cooking device or appliance with a composition comprising a built-in rinse aid |
| US9347025B2 (en) | 2008-12-02 | 2016-05-24 | Diversey, Inc. | Ware washing system containing cationic starch |
| US9161868B2 (en) | 2009-09-04 | 2015-10-20 | Kimberly-Clark Worldwide, Inc. | Removal of colored substances from aqueous liquids |
| US9161869B2 (en) | 2012-03-30 | 2015-10-20 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with decolorizing agents |
| US9220646B2 (en) | 2012-03-30 | 2015-12-29 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with improved stain decolorization |
| US9283127B2 (en) | 2012-03-30 | 2016-03-15 | Kimberly-Clark Worldwide, Inc. | Absorbent articles with decolorizing structures |
| US9237975B2 (en) | 2013-09-27 | 2016-01-19 | Kimberly-Clark Worldwide, Inc. | Absorbent article with side barriers and decolorizing agents |
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