EP3144373A1 - Neutral aqueous cleaning composition - Google Patents
Neutral aqueous cleaning composition Download PDFInfo
- Publication number
- EP3144373A1 EP3144373A1 EP15185397.5A EP15185397A EP3144373A1 EP 3144373 A1 EP3144373 A1 EP 3144373A1 EP 15185397 A EP15185397 A EP 15185397A EP 3144373 A1 EP3144373 A1 EP 3144373A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fatty acid
- composition
- alkoxylate
- cleaning
- methyl ester
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 71
- 238000004140 cleaning Methods 0.000 title claims abstract description 63
- 230000007935 neutral effect Effects 0.000 title claims abstract description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 20
- 239000000194 fatty acid Substances 0.000 claims abstract description 20
- 229930195729 fatty acid Natural products 0.000 claims abstract description 20
- 150000001412 amines Chemical class 0.000 claims abstract description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims description 32
- 239000002184 metal Substances 0.000 claims description 32
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims description 27
- 235000019387 fatty acid methyl ester Nutrition 0.000 claims description 26
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 claims description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- -1 alkyl dimethylamine oxide Chemical compound 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 5
- 229910000838 Al alloy Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000010935 stainless steel Substances 0.000 claims description 4
- 229910001220 stainless steel Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000006260 foam Substances 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- 239000004094 surface-active agent Substances 0.000 description 12
- 239000000356 contaminant Substances 0.000 description 11
- 238000005187 foaming Methods 0.000 description 10
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 240000002791 Brassica napus Species 0.000 description 6
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 6
- 238000013019 agitation Methods 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 230000007613 environmental effect Effects 0.000 description 6
- PVYJZLYGTZKPJE-UHFFFAOYSA-N streptonigrin Chemical compound C=1C=C2C(=O)C(OC)=C(N)C(=O)C2=NC=1C(C=1N)=NC(C(O)=O)=C(C)C=1C1=CC=C(OC)C(OC)=C1O PVYJZLYGTZKPJE-UHFFFAOYSA-N 0.000 description 6
- 239000002736 nonionic surfactant Substances 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000001804 emulsifying effect Effects 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 150000008282 halocarbons Chemical class 0.000 description 3
- 239000004530 micro-emulsion Substances 0.000 description 3
- ONLRKTIYOMZEJM-UHFFFAOYSA-N n-methylmethanamine oxide Chemical compound C[NH+](C)[O-] ONLRKTIYOMZEJM-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000004519 grease Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 150000003138 primary alcohols Chemical class 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- DQCMWCVJSOFDSA-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl.CC(Cl)(Cl)Cl DQCMWCVJSOFDSA-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical class C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229960001701 chloroform Drugs 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 238000011086 high cleaning Methods 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/825—Mixtures of compounds all of which are non-ionic
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/74—Carboxylates or sulfonates esters 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
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/16—Metals
Definitions
- the present invention belongs to the area of metal cleaning and refers to improved aqueous compositions for hard surface cleaning.
- a variety of metal cleaners have been used to clean such mechanical parts.
- solvent-based metal cleaners have been used which contain either halogenated or non-halogenated hydrocarbons.
- Aqueous-based, highly alkaline detergent systems have also been used to clean metal parts.
- solvent-based or aqueous-based cleaners has risen environmental and/or worker safety concerns.
- halogenated hydrocarbon solvents such as chlorofluorocarbons (CFCs), trichloromethane, methylene chloride and trichloroethane (methyl chloroform) have been widely used in industry for metal cleaning, the safety, environmental and cost factors associated with their use coupled with waste disposal problems are negative aspects of the use of such solvents.
- CFCs chlorofluorocarbons
- trichloromethane methylene chloride
- trichloroethane methyl chloroform
- Non-halogenated hydrocarbon solvents such as toluene, Stoddard solvent and like organic compounds such as ketones and alcohols are generally flammable and highly volatile and have dubious ability to be recycled for continuous use. These factors, along with unfavourable safety, environmental and cost factors make the non-halogenated hydrocarbon solvents unattractive for practical consideration.
- the most useful organic solvents classified as volatile organic compounds (VOCs), pollute the atmosphere, promote formation of a toxic zone at ground level, and add to the inventory of greenhouse gases.
- VOCs volatile organic compounds
- Aqueous cleaning systems have been developed to overcome some of the inherent negative environmental and health aspects associated with the solvent-based cleaning systems.
- EP 0782610 B1 discloses an organic solvent-free aqueous metal cleaning composition comprising at least one alkaline salt and a surfactant, said surfactant comprises from about 10 wt. % to about 50 wt.
- said surfactant consists essentially of non-phenolic alkoxylated non-ionic surfactants, N-alkyl pyrrolidones and mixtures thereof, an aqueous solution containing about 0.1 to about 20% of said composition being characterized as having complete phase separation ability of contaminants whereby the contaminants form a distinct and substantially complete phase from the aqueous solution, said composition having a phosphate content of less than 3 wt. % based on phosphorous, and having an initial foam
- EP 0908534 B1 covers an alkaline, aqueous metal-cleaning composition capable of effectively removing industrial-type soil contaminants from a metal surface at temperatures as low as ambient temperature and in the absence of substantial agitation contains (A) an active-ingredient portion containing an alkalinity-providing component, and a surfactant mixture containing: (a) at least one first non-ionic, ethoxylated linear primary alcohol surfactant having a hydrophobic carbon chain length of from 9 to 11 carbon atoms and being ethoxylated with (i) an average of 2.5 moles of ethylene oxide or (ii) an average of 5.0 moles of ethylene oxide; and (b) at least one second non-ionic, ethoxylated linear primary alcohol surfactant having a hydrophobic carbon chain length of from 9 to 11 carbon atoms and being ethoxylated with an average of 6.0 moles of ethylene oxide; and (B) an aqueous portion.
- A an active-ingredient portion
- EP 1590503 B1 discloses an aqueous cleaning composition for formed metal articles, the cleaning composition comprising (a) an adduct of 10 to 41 EO to a C 12 -C 25 aliphatic alcohol, (b) an inorganic pH adjusting component present in an amount such that the pH of the cleaning composition is less than 2; and (c) at least one non-ionic surfactant that is different than component (a) present in an amount from about 0.1 to about 3 g/l, wherein the cleaning composition has a water-break-free percent from 84% to 100%, and wherein the inorganic pH adjusting component comprises inorganic acid present in an amount of greater than 1 gram/litre to an amount of less than or equal to about 20 gram/litre of the cleaning composition.
- WO 2003 029393 A2 refers to cleaning compositions for metal surfaces, including both concentrate and ready-to-use solutions. These compositions include a source of calcium ion, a source of alkalinity, a chelating agent, and a surfactant; optionally a watersoluble or water-dispersible acid-substituted polymer is also included.
- the formulations are directed to cleaning compositions for metal surfaces, including both concentrate and ready-to-use solutions.
- US 8,697,622 BB (ECOLAB) is directed to synergistic combinations alkoxylated surfactants and co-surfactants, emulsions or micro-emulsions and cleaning compositions incorporating the same.
- a surfactant system which includes alkoxylated non-ionic surfactants, and a linker surfactant, particularly partial glycerides. This system forms stable emulsions or micro-emulsions with oils, including non-trans fats and fatty acids and these emulsions or micro-emulsions are stable, irreversible and can be created at low temperature.
- aqueous cleaning systems also have drawbacks.
- aqueous solutions used to clean industrial-type soil contaminants from metal surfaces are generally effective only at relatively high wash temperatures, 80 °C and above.
- Such high wash temperatures are disadvantageous because of the higher energy costs which are involved relative to lower temperature washing and the difficulty with maintaining such high temperatures.
- a reduced wash temperature usually leads to reduced cleaning versus that obtained at higher wash temperatures. It would be desirable, therefore, to provide an aqueous metal-cleaning composition which provides high cleaning performance at relatively low wash temperatures.
- aqueous cleaners stems from the high surface tension of water and the propensity of the detersive agents in the aqueous cleaner to foam upon agitation of the cleaning bath such as induced in the bath or by the use of spray nozzles to apply the cleaning solution to the metal components being cleaned.
- the foaming profile of an aqueous cleaner is an important characteristic. The presence of foam often renders the use of machines with high mechanical agitation impractical due to excessive foaming. High foaming cleaners are particularly problematic in spray equipment. In addition to foam exiting the equipment, foaming can cause pump cavitation and selective loss of surfactants.
- foaming does not contribute to cleaning and, therefore, is not necessary for immersion or spray cleaning.
- low foaming cleaners are preferred because they can be used in dip, immersion, ultrasonic and spray equipment.
- agitation of the cleaning solution appears to induce foaming.
- one way to reduce foam formation would be to reduce or eliminate the agitation of the cleaning solution. It would be desirable, therefore, to provide an aqueous metal-cleaning composition which is capable of substantially removing industrial-type soil contaminants from metal surfaces at low wash temperatures without substantial agitation of the cleaning composition, thereby avoiding excessive foaming during use of the composition.
- These exceedingly alkaline aqueous solutions are highly corrosive to metal surfaces, highly toxic and can be dangerous to handle, thus requiring extreme safety measures to avoid contact with the skin.
- Organic solvent-containing aqueous cleaners have the toxicity and environmental problems discussed previously herein.
- aqueous metal cleaners be reusable to render such cleaners economically viable.
- Many of the aqueous-based cleaners now available use detersive agents which are effective in removing the dirt, grease or oil from the metal surface but which unfortunately readily emulsify the contaminants such that the contaminants are highly dispersed or solubilized throughout the aqueous solution.
- These highly emulsified cleaning solutions are difficult to treat to separate the contaminants from the aqueous cleaner and, accordingly, the cleaning solution gets spent in a relatively short period of time and must be replaced to again achieve effective cleaning of the metal parts and the like.
- It would be desirable to provide an aqueous metal cleaner which could effectively remove the contaminants from the metal surface but which would allow the ready separation of such contaminants from the cleaning solution to allow effective and prolonged reuse of the solution
- the problem underlying the present invention has been to provide a low-temperature aqueous metal cleaning composition which is not highly corrosive to metal surfaces, and exhibits simultaneously improved cleaning performance, high emulsifying capacity and low foaming behaviour.
- the new composition should be environmental friendly, particularly free of boron compounds, and safe to humans.
- a first object of the present invention is a neutral aqueous cleaning composition comprising
- the aqueous compositions according to the present invention fully comply with the complex profile described above.
- the compositions provide superior cleaning performance when compared with products one can find in the market. They also show higher emulsifying capacity and thus higher shelf time, and they either do not exhibit foam at all or the foam collapses in very short time.
- the formulations can easily be reused or run in cycles.
- the compositions are either fully or in the alternative to a major extend based on renewable sources, not corrosive to metal surfaces, readily biodegradable and safe to skin.
- Adducts of alkylene oxides which includes ethylene oxide, propylene oxide, butylene oxides and their mixtures
- They belong to the group of non-ionic surfactants, although they are less common as for example adducts of AO to fatty alcohols.
- the acyl moiety of the molecules can be derived from individual fatty acids, but preferably from technical sources as for example coconut oil, palm oil, palm kernel oil, olive oil, soy oil and in particular rape seed oil.
- the chain length of the acyl radical differs between 12 and 22; preferred alternatives are those having a focus on C 12 -C 14 or C 16 -C 18 .
- the acyl group may be saturated or unsaturated, in the latter case having 1, 2 or 3 double bonds. Typically, the acyl group represents a mixture of species having different chain lengths and numbers of double bonds.
- fatty acid alkyl ester alkoxylates are fatty acid methyl ester alkoxylates.
- fatty acid alkyl ester alkoxylates are fatty acid alkyl ester ethoxylates.
- the preferred species encompass the following individuals:
- the alkoxylates follow general formula (III) R 7 (OCH 2 CHR 8 ) m OH (III) in which R 7 stands for an alkyl group having 6 to 12 carbon atoms, R 8 means either hydrogen or methyl and m represents an integer of from 2 to 10.
- R 7 stands for an alkyl group having 6 to 12 carbon atoms
- R 8 means either hydrogen or methyl
- m represents an integer of from 2 to 10.
- the preferred alcohol alkoxylates are chosen from the following individuals:
- Amine oxides, forming component (c) of the composition according to the present invention are well-known non-ionic surfactants, which work as hydrotropes.
- the compounds follow general formula (I) in which R 1 stands for an alkyl group having 10 to 14, preferably 12 to 14 carbon atoms and R 2 and R 3 independently from each other for hydrogen or an alkyl group having 1 to 4 carbon atoms.
- the preferred amine oxide is C 12/14 alkyl dimethylamine oxide.
- compositions show a pH-value of from about 5 to about 8 and more preferably of about 7. It should be understood that the preferred embodiments with regard to specific chain length and degree of ethoxylation as explained above also apply for the compositions without being repeated again.
- Another object of the present invention is related to a method for cleaning hard surfaces, comprising the following steps:
- the present invention also encompasses the use of the neutral cleaning composition as described above for cleaning hard surfaces particularly made from stainless steel, copper metals and/or aluminium alloys.
- Table 1 The results are compiled in Table 1 .
- Examples 1 to 3 are according to the invention, Comparison examples C1 and C2 refer to market products (C1: “Bike Clean” (Motorex); C2: “Nigrin Performance” (Evotec).
- compositions according to the present invention provide a significantly superior cleaning performance.
- compositions according to the present invention provide significant a lower foaming power.
- compositions according to the present invention provide emulsions with significantly higher emulsion stability.
Landscapes
- 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
(a) at least one fatty acid alkyl ester alkoxylate, and
(b) at least one alcohol alkoxylate; and
(c) at least one amine oxide,
Description
- The present invention belongs to the area of metal cleaning and refers to improved aqueous compositions for hard surface cleaning.
- Many industries, such as, for example, lubricants and automobile parts repair and replacement services and the like, require that component mechanical parts be cleaned prior to inspection, repair, or replacement thereof. Generally, such parts have been exposed to various industrial-type soil contaminants such as dirt, grease, oil, ink and the like, which must be removed for effective repair or service.
- A variety of metal cleaners have been used to clean such mechanical parts. For example, solvent-based metal cleaners have been used which contain either halogenated or non-halogenated hydrocarbons. Aqueous-based, highly alkaline detergent systems have also been used to clean metal parts. However, the use of such solvent-based or aqueous-based cleaners has risen environmental and/or worker safety concerns.
- For example, although halogenated hydrocarbon solvents such as chlorofluorocarbons (CFCs), trichloromethane, methylene chloride and trichloroethane (methyl chloroform) have been widely used in industry for metal cleaning, the safety, environmental and cost factors associated with their use coupled with waste disposal problems are negative aspects of the use of such solvents. A world-wide and U.S. ban on most halogenated solvents is soon in the offing by virtue of the Montreal Protocol, Clean Air Act and Executive and Departmental directives.
- Non-halogenated hydrocarbon solvents such as toluene, Stoddard solvent and like organic compounds such as ketones and alcohols are generally flammable and highly volatile and have dubious ability to be recycled for continuous use. These factors, along with unfavourable safety, environmental and cost factors make the non-halogenated hydrocarbon solvents unattractive for practical consideration. For example, the most useful organic solvents, classified as volatile organic compounds (VOCs), pollute the atmosphere, promote formation of a toxic zone at ground level, and add to the inventory of greenhouse gases.
- Aqueous cleaning systems have been developed to overcome some of the inherent negative environmental and health aspects associated with the solvent-based cleaning systems.
- For example
EP 0782610 B1 (CHURCH & DWIGHT ) discloses an organic solvent-free aqueous metal cleaning composition comprising at least one alkaline salt and a surfactant, said surfactant comprises from about 10 wt. % to about 50 wt. % of the cleaning composition based on dry components of the cleaning composition, said surfactant consists essentially of non-phenolic alkoxylated non-ionic surfactants, N-alkyl pyrrolidones and mixtures thereof, an aqueous solution containing about 0.1 to about 20% of said composition being characterized as having complete phase separation ability of contaminants whereby the contaminants form a distinct and substantially complete phase from the aqueous solution, said composition having a phosphate content of less than 3 wt. % based on phosphorous, and having an initial foam -
EP 0908534 B1 (CHURCH & DWIGHT ) covers an alkaline, aqueous metal-cleaning composition capable of effectively removing industrial-type soil contaminants from a metal surface at temperatures as low as ambient temperature and in the absence of substantial agitation contains (A) an active-ingredient portion containing an alkalinity-providing component, and a surfactant mixture containing: (a) at least one first non-ionic, ethoxylated linear primary alcohol surfactant having a hydrophobic carbon chain length of from 9 to 11 carbon atoms and being ethoxylated with (i) an average of 2.5 moles of ethylene oxide or (ii) an average of 5.0 moles of ethylene oxide; and (b) at least one second non-ionic, ethoxylated linear primary alcohol surfactant having a hydrophobic carbon chain length of from 9 to 11 carbon atoms and being ethoxylated with an average of 6.0 moles of ethylene oxide; and (B) an aqueous portion. -
EP 1590503 B1 (HENKEL ) discloses an aqueous cleaning composition for formed metal articles, the cleaning composition comprising (a) an adduct of 10 to 41 EO to a C12-C25 aliphatic alcohol, (b) an inorganic pH adjusting component present in an amount such that the pH of the cleaning composition is less than 2; and (c) at least one non-ionic surfactant that is different than component (a) present in an amount from about 0.1 to about 3 g/l, wherein the cleaning composition has a water-break-free percent from 84% to 100%, and wherein the inorganic pH adjusting component comprises inorganic acid present in an amount of greater than 1 gram/litre to an amount of less than or equal to about 20 gram/litre of the cleaning composition. -
WO 2003 029393 A2 (ECOLAB) refers to cleaning compositions for metal surfaces, including both concentrate and ready-to-use solutions. These compositions include a source of calcium ion, a source of alkalinity, a chelating agent, and a surfactant; optionally a watersoluble or water-dispersible acid-substituted polymer is also included. The formulations are directed to cleaning compositions for metal surfaces, including both concentrate and ready-to-use solutions. - Finally,
US 8,697,622 BB - Unfortunately, aqueous cleaning systems also have drawbacks. For example, aqueous solutions used to clean industrial-type soil contaminants from metal surfaces are generally effective only at relatively high wash temperatures, 80 °C and above. Such high wash temperatures are disadvantageous because of the higher energy costs which are involved relative to lower temperature washing and the difficulty with maintaining such high temperatures. Unfortunately, with aqueous solutions, a reduced wash temperature usually leads to reduced cleaning versus that obtained at higher wash temperatures. It would be desirable, therefore, to provide an aqueous metal-cleaning composition which provides high cleaning performance at relatively low wash temperatures.
- Another advantage associated with the use of aqueous cleaners stems from the high surface tension of water and the propensity of the detersive agents in the aqueous cleaner to foam upon agitation of the cleaning bath such as induced in the bath or by the use of spray nozzles to apply the cleaning solution to the metal components being cleaned. The foaming profile of an aqueous cleaner is an important characteristic. The presence of foam often renders the use of machines with high mechanical agitation impractical due to excessive foaming. High foaming cleaners are particularly problematic in spray equipment. In addition to foam exiting the equipment, foaming can cause pump cavitation and selective loss of surfactants. Also, the presence of foam can cause the overflow of liquids onto floors as well as cause difficulties with viewing the cleaning process through vision ports and the like contained in the machinery. Contrary to popular belief, foaming does not contribute to cleaning and, therefore, is not necessary for immersion or spray cleaning. Generally, low foaming cleaners are preferred because they can be used in dip, immersion, ultrasonic and spray equipment.
- It has been found that, in conventional aqueous metal-cleaning compositions, foam formation will decrease with increased temperature. Thus, with such compositions, the use of relatively low wash temperatures tends to lead to high foam formation, which renders such cleaning compositions unsuitable for use at low temperatures.
- As stated above, agitation of the cleaning solution appears to induce foaming. Thus, one way to reduce foam formation would be to reduce or eliminate the agitation of the cleaning solution. It would be desirable, therefore, to provide an aqueous metal-cleaning composition which is capable of substantially removing industrial-type soil contaminants from metal surfaces at low wash temperatures without substantial agitation of the cleaning composition, thereby avoiding excessive foaming during use of the composition.
- A further drawback associated with aqueous cleaners containing sodium hydroxide or organic solvents such as alkanolamines, ethers, alcohols, glycols and the like, is that such cleaners tend to be exceedingly alkaline, i.e., having pH values of 13 and above. These exceedingly alkaline aqueous solutions are highly corrosive to metal surfaces, highly toxic and can be dangerous to handle, thus requiring extreme safety measures to avoid contact with the skin. Organic solvent-containing aqueous cleaners have the toxicity and environmental problems discussed previously herein.
- It is also important that the aqueous metal cleaners be reusable to render such cleaners economically viable. Thus, it is not practical on an industrial scale to sewer an aqueous cleaning bath upon a single usage thereof. Many of the aqueous-based cleaners now available use detersive agents which are effective in removing the dirt, grease or oil from the metal surface but which unfortunately readily emulsify the contaminants such that the contaminants are highly dispersed or solubilized throughout the aqueous solution. These highly emulsified cleaning solutions are difficult to treat to separate the contaminants from the aqueous cleaner and, accordingly, the cleaning solution gets spent in a relatively short period of time and must be replaced to again achieve effective cleaning of the metal parts and the like. It would be desirable to provide an aqueous metal cleaner which could effectively remove the contaminants from the metal surface but which would allow the ready separation of such contaminants from the cleaning solution to allow effective and prolonged reuse of the solution
- Therefore, the problem underlying the present invention has been to provide a low-temperature aqueous metal cleaning composition which is not highly corrosive to metal surfaces, and exhibits simultaneously improved cleaning performance, high emulsifying capacity and low foaming behaviour. Finally, the new composition should be environmental friendly, particularly free of boron compounds, and safe to humans.
- A first object of the present invention is a neutral aqueous cleaning composition comprising
- (a) at least one fatty acid alkyl ester alkoxylate,
- (b) at least one alcohol alkoxylate, and
- (c) at least one amine oxide,
- Surprisingly, it has been observed that the aqueous compositions according to the present invention fully comply with the complex profile described above. In particular the compositions provide superior cleaning performance when compared with products one can find in the market. They also show higher emulsifying capacity and thus higher shelf time, and they either do not exhibit foam at all or the foam collapses in very short time. The formulations can easily be reused or run in cycles. The compositions are either fully or in the alternative to a major extend based on renewable sources, not corrosive to metal surfaces, readily biodegradable and safe to skin.
- Adducts of alkylene oxides (which includes ethylene oxide, propylene oxide, butylene oxides and their mixtures) - form component (a) of the present invention. They belong to the group of non-ionic surfactants, although they are less common as for example adducts of AO to fatty alcohols. Preferably they follow general formula (II)
R4CO-(OCH2CHR5)nOR6 (II)
in which R4CO stands for a saturated or unsaturated, linear or branched acyl radical having 12 to 22 carbon atoms, R5 means either hydrogen or methyl, R6 stands for an alkyl group having 1 to 4 carbon atoms and n represents an integer of from 5 to 12, and preferably 7 to 10. The acyl moiety of the molecules can be derived from individual fatty acids, but preferably from technical sources as for example coconut oil, palm oil, palm kernel oil, olive oil, soy oil and in particular rape seed oil. The chain length of the acyl radical differs between 12 and 22; preferred alternatives are those having a focus on C12-C14 or C16-C18. The acyl group may be saturated or unsaturated, in the latter case having 1, 2 or 3 double bonds. Typically, the acyl group represents a mixture of species having different chain lengths and numbers of double bonds. - In a preferred embodiment the fatty acid alkyl ester alkoxylates are fatty acid methyl ester alkoxylates.
- In another preferred embodiment the fatty acid alkyl ester alkoxylates are fatty acid alkyl ester ethoxylates.
- The overall preferred fatty acid alkyl ester alkoxylates encompass
- (b1) a C12/18 fatty acid methyl ester ethoxylate and/or
- (b2) a C16/18 fatty acid methyl ester ethoxylate.
- More particular, the preferred species encompass the following individuals:
- C12/18 fatty acid methyl ester + 7EO;
- C12/18 fatty acid methyl ester + 10EO;
- C16/18 fatty acid methyl ester + 7EO;
- C16/18 fatty acid methyl ester + 10EO;
- The results from the application examples show that it is advantageous to use a composition comprising at least two different fatty acid alkyl ester ethoxylates, differing in acyl chain length and/or degree of alkoxylation.
- Adducts of alkylene oxide to alcohols, preferably aliphatic alcohols, form component (b). Preferably the alkoxylates follow general formula (III)
R7(OCH2CHR8)mOH (III)
in which R7 stands for an alkyl group having 6 to 12 carbon atoms, R8 means either hydrogen or methyl and m represents an integer of from 2 to 10. The preferred alcohol alkoxylates are chosen from the following individuals: - Octanol+2.5EO;
- Octanol+4EO;
- Octanol+6EO;
- Octanol+8EO;
- Octanol+10EO;
- Decanol+2.5EO
- Decanol-4EO
- Decanol+6EO;
- Decanol+8EO;
- Decanol+10 EO;
- Amine oxides, forming component (c) of the composition according to the present invention, are well-known non-ionic surfactants, which work as hydrotropes. Preferably the compounds follow general formula (I)
- In another preferred embodiment the composition of the present invention comprise
- (a) about 0.1 to about 10 % b.w., preferably about 1 to about 8 % b.w., more preferably about 2 to about 5 % b.w. of at least one fatty acid alkyl ester alkoxylate;
- (b) about 0.1 to about 8 % b.w., preferably about 1 to about 6 % b.w., more preferably about 2 to about 5 % b.w. of at least one alcohol alkoxylate; and
- (c) about 0.1 to about 10 % b.w., preferably about 0.5 to 5 % b.w., more preferably about 0.9 to about 3 % b.w. of at least one amine oxide;
on condition that the amounts add with water and optionally further additives to 100 % b.w. - Preferably the compositions show a pH-value of from about 5 to about 8 and more preferably of about 7. It should be understood that the preferred embodiments with regard to specific chain length and degree of ethoxylation as explained above also apply for the compositions without being repeated again.
- Another object of the present invention is related to a method for cleaning hard surfaces, comprising the following steps:
- (a) providing a hard surface, said surface being made of stainless steel, copper metals or aluminium alloys;
- (b) bringing said hard surface in contact with an amount of the neutral cleaning composition of the present invention sufficient to clean the surface; and
- (c) cleaning said surface by removing the cleaner along with the stains.
- Finally, the present invention also encompasses the use of the neutral cleaning composition as described above for cleaning hard surfaces particularly made from stainless steel, copper metals and/or aluminium alloys.
- EXAMPLES 1 to 3, Comparative Examples C1 and C2
- For evaluating the cleaning power the lower parts of a tared plate were dipped into motor oil. After sticked oil had dripped off, the plates were weighed. Subsequently the lower part of said plate was dipped into a 100 ml beaker glass containing 90 g of a cleaning composition. The solution was stirred for 10 minutes at 20 °C at 1.000 rpm. The plates were removed and dried for 10 minutes at 105 °C. Finally the plates were weighed again and cleaning performance calculated according to the following equation:
- The results are compiled in Table 1. Examples 1 to 3 are according to the invention, Comparison examples C1 and C2 refer to market products (C1: "Bike Clean" (Motorex); C2: "Nigrin Performance" (Evotec).
Table 1 Cleaning power Composition 1 2 3 C1 C2 Libranox AO12/14 (30 % b.w. solution) 10,0 10,0 10,0 C12/14 dimethylamine oxide Greenbentin XES/070 2.0 2.0 - C16/18 Rapeseed fatty acid methyl ester + 7EO Greenbentin XES/100 2.0 2.0 - C16/18 Rapeseed fatty acid methyl ester + 10EO Greenbentin MLS/070 - - 2.0 C12/14 fatty acid methyl ester + 7EO Greenbentin MLS/100 - - 2.0 C12/14 fatty acid methyl ester + 7EO Greenbentin DE/060 2.0 - - Decanol+6EO Greenbentin DE/080 - 2.0 2.0 Decanol+8EO pH-value 7.25 7.09 7.29 8.98 5.13 Water Ad 100 Cleaning performance (%) 87 85 87 76 76 - The examples and comparative examples clearly demonstrate that the compositions according to the present invention provide a significantly superior cleaning performance.
- EXAMPLES 4 to 6, Comparative Examples C3 and C4
- For evaluating the foam behavior 40 ml of five different cleaners were placed at room temperature in 100 ml glass cylinders and shaken for 30 seconds. Subsequently foam heights after 5, 10 and 15 minutes were determined. The results are compiled in Table 2. Examples 4 to 6 are according to the invention, Comparison examples C3 and C4 refer to market products (C3: "Bike Clean" (Motorex); C4: "Nigrin Performance" (Evotec).
Table 2 Foam behavior Composition 4 5 6 C3 C4 Libranox AO12/14 (30 % b.w. solution) 10,0 10,0 10,0 C12/14 dimethylamine oxide Greenbentin XES/070 2.0 2.0 - C16/18 Rapeseed fatty acid methyl ester + 7EO Greenbentin XES/100 2.0 2.0 - C16/18 Rapeseed fatty acid methyl ester + 10EO Greenbentin MLS/070 - - 2.0 C12/14 fatty acid methyl ester + 7EO Greenbentin MLS/100 - - 2.0 C12/14 fatty acid methyl ester + 7EO Greenbentin DE/060 2.0 - - Decanol+6EO Greenbentin DE/080 - 2.0 2.0 Decanol+8EO pH-value 7.25 7.09 7.29 8.98 5.13 Water Ad 100 Foam heights (mm) - after 5 min 90 45 100 100 100 - after 10 minutes 58 43 55 100 100 - after 15 minutes 51 42 42 55 100 - The examples and comparative examples clearly demonstrate that the compositions according to the present invention provide significant a lower foaming power.
- EXAMPLES 7 to 9, Comparative Examples C5 and C6
- For evaluating the emulsifying capacity 80 ml of five different cleaners and 20 ml Vaseline oil were mixed by Ultraturrax (20 °C, 2 min, 8.400 rpm). Subsequently the amount of water recovered from the emulsion was determined. The results are compiled in Table 3. Examples 7 to 9 are according to the invention, Comparison examples C5 and C6 refer to market products (C5: "Bike Clean" (Motorex); C6: "Nigrin Performance" (Evotec).
Table 3 Emulsifying capacity Composition 7 8 9 C5 C6 Libranox AO12/14 (30 % b.w. solution) 10,0 10,0 10,0 C12/14 dimethylamine oxide Greenbentin XES/070 2.0 2.0 - C16/18 Rapeseed fatty acid methyl ester + 7EO Greenbentin XES/100 2.0 2.0 - C16/18 Rapeseed fatty acid methyl ester + 10EO Greenbentin MLS/070 - - 2.0 C12/14 fatty acid methyl ester + 7EO Greenbentin MLS/100 - - 2.0 C12/14 fatty acid methyl ester + 7EO Greenbentin DE/060 2.0 - - Decanol+6EO Greenbentin DE/080 - 2.0 2.0 Decanol+8EO pH-value 7.25 7.09 7.29 8.98 5.13 Water Ad 100 Water recovery (%) - after 0.5 h 18 21 7 20 22 - after 1 h 36 38 7 42 45 - after 2 h 58 58 7 58 60 - after 3 h 62 63 7 76 76 - after 5 h 65 65 50 85 87 - The examples and comparative examples clearly demonstrate that the compositions according to the present invention provide emulsions with significantly higher emulsion stability.
Claims (15)
- A neutral aqueous cleaning composition comprising(a) at least one fatty acid alkyl ester alkoxylate,(b) at least one alcohol alkoxylate, and(c) at least one amine oxide,
- The composition of claim 1, wherein the fatty acid alkyl ester alkoxylate follows general formula (II)
R4CO-(OCH2CHR5)nOR6 (II)
in which R4CO stands for a saturated or unsaturated, linear or branched acyl radical having 12 to 22 carbon atoms, R5 means either hydrogen or methyl, R6 stands for an alkyl group having 1 to 4 carbon atoms and n represents an integer of from 5 to 12. - The composition of Claim 1, wherein the fatty acid alkyl ester alkoxylate is a fatty acid methyl ester alkoxylate.
- The composition of Claim 1, wherein the fatty acid alkyl ester alkoxylate is a fatty acid alkyl ester ethoxylate.
- The composition of Claim 1, wherein the fatty acid alkyl ester alkoxylate is(b1) a C12/18 fatty acid methyl ester ethoxylate and/or(b2) a C16/18 fatty acid methyl ester ethoxylate.
- The composition of Claim 1, wherein the fatty acid alkyl ester alkoxylate is selected from the group consisting of the following individuals:C12/18 fatty acid methyl ester + 7EO;C12/18 fatty acid methyl ester + 10EO;C16/18 fatty acid methyl ester + 7EO;C16/18 fatty acid methyl ester + 10EO;and mixtures thereof.
- The composition of Claim 1, comprising at least two different fatty acid alkyl ester ethoxylates, differing in acyl chain length and/or degree of alkoxylation.
- The composition of Claim 1, wherein the alcohol alkoxylate (compound c) follows general formula (III)
R7(OCH2CHR8)mOH (III)
In which R7 stands for an alkyl group having 6 to 12 carbon atoms, R8 means either hydrogen or methyl and m represents an integer of from 2 to 10. - The composition of Claim 1, wherein the alcohol alkoxylate is selected from the group consisting of the following individuals:Octanol+2.5EO;Octanol+4EO;Octanol+6EO;Octanol+8EO;Octanol+10EO;Decanol+2.5EO Decanol+4EO Decanol+6EO;Decanol+8EO;Decanol+10 EO;and mixtures thereof.
- The composition of Claim 1, wherein the amine oxide is C12/14 alkyl dimethylamine oxide.
- The composition of Claim 1 comprising(a) about 0.1 to about 10 % b.w. of at least one fatty acid alkyl ester alkoxylate;(b) about 0.1 to about 8 % b.w. of at least one alcohol alkoxylate; and(c) about 0.1 to about 10 % b.w. of at least one amine oxide;
on condition that the amounts add with water and optionally further additives to 100 % b.w. - The composition of Claim 1 having a pH-value of from about 5 to about 8.
- A method for cleaning hard surfaces, comprising the following steps:(a) providing a hard surface, said surface being made of stainless steel, copper metals or aluminium alloys;(b) bringing said hard surface in contact with an amount of the neutral cleaning composition of claim 1 sufficient to clean the surface; and(c) cleaning said surface by removing the cleaner along with the stains.
- Use of the neutral cleaning composition of Claim 1 for cleaning hard surfaces particularly made from stainless steel, copper metals and/or aluminium alloys.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP15185397.5A EP3144373B1 (en) | 2015-09-16 | 2015-09-16 | Neutral aqueous cleaning composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP15185397.5A EP3144373B1 (en) | 2015-09-16 | 2015-09-16 | Neutral aqueous cleaning composition |
Publications (2)
Publication Number | Publication Date |
---|---|
EP3144373A1 true EP3144373A1 (en) | 2017-03-22 |
EP3144373B1 EP3144373B1 (en) | 2018-12-26 |
Family
ID=54147077
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP15185397.5A Active EP3144373B1 (en) | 2015-09-16 | 2015-09-16 | Neutral aqueous cleaning composition |
Country Status (1)
Country | Link |
---|---|
EP (1) | EP3144373B1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108251228A (en) * | 2018-02-12 | 2018-07-06 | 广州蓝月亮实业有限公司 | A kind of detergent composition |
EP3744819A1 (en) | 2019-05-26 | 2020-12-02 | Fama Holding AG | Composition with alkoxylated fatty acids |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4326112A1 (en) * | 1993-08-04 | 1995-02-09 | Henkel Kgaa | Detergent for hard surfaces |
EP0782610A1 (en) | 1994-09-23 | 1997-07-09 | CHURCH & DWIGHT COMPANY, INC. | Aqueous metal cleaner |
US5922669A (en) * | 1997-09-10 | 1999-07-13 | Albemarle Corporation | No-rub hard surface cleaner comprising an alcohol ethoxylate-amine oxide surfactant mixture and a nitrogenous builder in aqueous solution |
WO2003029393A2 (en) | 2001-09-28 | 2003-04-10 | Ecolab Inc. | Alkaline metal cleaner |
EP0908534B1 (en) | 1997-09-16 | 2003-10-29 | CHURCH & DWIGHT COMPANY, INC. | Aqueous composition for low-temperature metal-cleaning and method of use |
US20100305018A1 (en) * | 2007-08-29 | 2010-12-02 | Basf Se | Esterified alkyl alkoxylates as solid low-foam wetters |
EP1590503B1 (en) | 2003-01-23 | 2011-12-21 | Henkel AG & Co. KGaA | Cleaner composition for formed metal articles |
US20120021963A1 (en) * | 2010-07-23 | 2012-01-26 | American Sterilizer Company | Biodegradable concentrated neutral detergent composition |
US20130338420A1 (en) * | 2012-06-19 | 2013-12-19 | The Procter & Gamble Company | Surfactant Composition and Method for Decontamination |
US8697622B2 (en) | 2010-09-17 | 2014-04-15 | Ecolab Usa Inc. | Cleaning compositions and emulsions or microemulsions employing extended chain nonionic surfactants |
-
2015
- 2015-09-16 EP EP15185397.5A patent/EP3144373B1/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4326112A1 (en) * | 1993-08-04 | 1995-02-09 | Henkel Kgaa | Detergent for hard surfaces |
EP0782610A1 (en) | 1994-09-23 | 1997-07-09 | CHURCH & DWIGHT COMPANY, INC. | Aqueous metal cleaner |
US5922669A (en) * | 1997-09-10 | 1999-07-13 | Albemarle Corporation | No-rub hard surface cleaner comprising an alcohol ethoxylate-amine oxide surfactant mixture and a nitrogenous builder in aqueous solution |
EP0908534B1 (en) | 1997-09-16 | 2003-10-29 | CHURCH & DWIGHT COMPANY, INC. | Aqueous composition for low-temperature metal-cleaning and method of use |
WO2003029393A2 (en) | 2001-09-28 | 2003-04-10 | Ecolab Inc. | Alkaline metal cleaner |
EP1590503B1 (en) | 2003-01-23 | 2011-12-21 | Henkel AG & Co. KGaA | Cleaner composition for formed metal articles |
US20100305018A1 (en) * | 2007-08-29 | 2010-12-02 | Basf Se | Esterified alkyl alkoxylates as solid low-foam wetters |
US20120021963A1 (en) * | 2010-07-23 | 2012-01-26 | American Sterilizer Company | Biodegradable concentrated neutral detergent composition |
US8697622B2 (en) | 2010-09-17 | 2014-04-15 | Ecolab Usa Inc. | Cleaning compositions and emulsions or microemulsions employing extended chain nonionic surfactants |
US20130338420A1 (en) * | 2012-06-19 | 2013-12-19 | The Procter & Gamble Company | Surfactant Composition and Method for Decontamination |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108251228A (en) * | 2018-02-12 | 2018-07-06 | 广州蓝月亮实业有限公司 | A kind of detergent composition |
EP3744819A1 (en) | 2019-05-26 | 2020-12-02 | Fama Holding AG | Composition with alkoxylated fatty acids |
Also Published As
Publication number | Publication date |
---|---|
EP3144373B1 (en) | 2018-12-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109628947B (en) | Environment-friendly neutral cleaning agent and preparation method and application thereof | |
CA2245429C (en) | Aqueous composition for low-temperature metal-cleaning and method of use | |
AU726452B2 (en) | Low-foam cleaning agent | |
DE69529832T2 (en) | AQUEOUS METAL CLEANER | |
US5614027A (en) | Metal cleaner with novel anti-corrosion system | |
JP2523111B2 (en) | Demulsifying detergent formulation | |
JPH05504155A (en) | Demulsifying cleaning preparations and their uses | |
US4514325A (en) | Aqueous metal treating compositions and method of use | |
EP3144373B1 (en) | Neutral aqueous cleaning composition | |
JPH06192693A (en) | Aqueous detergent composition | |
JPH04136194A (en) | Cleaning method | |
WO2006058570A1 (en) | Metal cleaner containing polyethylenimine | |
US5866528A (en) | Aqueous cleaning composition for cleaning substrates and method of using same | |
WO1998050505A1 (en) | Aqueous cleaning composition for cleaning substrates and method of using same | |
EP1578893B1 (en) | Degreasing compositions | |
CN108865491A (en) | A kind of efficiently stripping oil type industrial greasy dirt cleaning agent and preparation method | |
EP4025109B1 (en) | Cleaning robot comprising a cleaning cloth and cleaning means | |
DE4102709C1 (en) | Degreasing metal surfaces using aq. prepn. - contg. biologically degradable adducts of lower alkylene oxide(s), fatty alcohol(s) and cationic surfactants | |
JPH07268674A (en) | Detergent composition for metallic product | |
KR100447429B1 (en) | Detergent composition having excellent anti-corrosive property and powerful cleaning effect | |
JPH06336600A (en) | Cleaning composition and cleaning method | |
KR970007569B1 (en) | Neutral detergent and its method | |
JP5480491B2 (en) | Cleaning composition for parts box and cleaning method using the same | |
RU2752674C1 (en) | Cleaning substance | |
US5849683A (en) | Aqueous cleaning composition for cleaning substrates and method of using same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN PUBLISHED |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
AX | Request for extension of the european patent |
Extension state: BA ME |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20170915 |
|
RBV | Designated contracting states (corrected) |
Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20180620 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAJ | Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR1 |
|
GRAL | Information related to payment of fee for publishing/printing deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR3 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
GRAJ | Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR1 |
|
GRAL | Information related to payment of fee for publishing/printing deleted |
Free format text: ORIGINAL CODE: EPIDOSDIGR3 |
|
INTC | Intention to grant announced (deleted) | ||
GRAR | Information related to intention to grant a patent recorded |
Free format text: ORIGINAL CODE: EPIDOSNIGR71 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
INTC | Intention to grant announced (deleted) | ||
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
INTG | Intention to grant announced |
Effective date: 20181119 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: REF Ref document number: 1081416 Country of ref document: AT Kind code of ref document: T Effective date: 20190115 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602015022165 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190326 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190326 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20181226 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: RS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: AL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190327 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1081416 Country of ref document: AT Kind code of ref document: T Effective date: 20181226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190426 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SM Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190426 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602015022165 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20190927 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190916 Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190916 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20190930 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190930 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20150916 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181226 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20240919 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20240923 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20240930 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 20241001 Year of fee payment: 10 |