EP3011002A1 - Mittel zur entfernung von flecken und ablagerungen - Google Patents
Mittel zur entfernung von flecken und ablagerungenInfo
- Publication number
- EP3011002A1 EP3011002A1 EP14731263.1A EP14731263A EP3011002A1 EP 3011002 A1 EP3011002 A1 EP 3011002A1 EP 14731263 A EP14731263 A EP 14731263A EP 3011002 A1 EP3011002 A1 EP 3011002A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- agent
- copolymers
- styrene
- weight
- stains
- 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
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- 150000001342 alkaline earth metals Chemical class 0.000 description 1
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- 239000000908 ammonium hydroxide Substances 0.000 description 1
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- 235000019418 amylase Nutrition 0.000 description 1
- 229940025131 amylases Drugs 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- 229960000686 benzalkonium chloride Drugs 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 229960003168 bronopol Drugs 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
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- 230000000052 comparative effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000004064 cosurfactant Substances 0.000 description 1
- 229940071118 cumenesulfonate Drugs 0.000 description 1
- 235000021438 curry Nutrition 0.000 description 1
- 150000007973 cyanuric acids Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007257 deesterification reaction Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 229940088598 enzyme Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229960000587 glutaral Drugs 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000002649 leather substitute Substances 0.000 description 1
- 229940040102 levulinic acid Drugs 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000012476 oxidizable substance Substances 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 150000004965 peroxy acids Chemical class 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 230000001699 photocatalysis Effects 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000036316 preload Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940079842 sodium cumenesulfonate Drugs 0.000 description 1
- QEKATQBVVAZOAY-UHFFFAOYSA-M sodium;4-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=C(S([O-])(=O)=O)C=C1 QEKATQBVVAZOAY-UHFFFAOYSA-M 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
-
- 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
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/042—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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/04—Water-soluble compounds
- C11D3/044—Hydroxides or bases
-
- 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
- C11D3/18—Hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
-
- 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
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3749—Polyolefins; Halogenated polyolefins; Natural or synthetic rubber; Polyarylolefins or halogenated polyarylolefins
-
- 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
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
-
- 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
- C11D3/395—Bleaching agents
-
- 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
- C11D3/43—Solvents
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- 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
- C11D2111/12—Soft surfaces, e.g. textile
-
- 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
Definitions
- the present invention relates to agents useful for removing a variety of different stains and deposits on hard and soft surfaces.
- the agent is suitable for removing hard-to-remove stains from soft, delicate materials such as textiles.
- the stains can be spots on the underarm area of garments, but also stains of chocolate, lipstick, shoe polish, red wine, turmeric, fat, lime, soap scum, feces, rust, blood and chewing gum.
- composition according to the invention is also suitable for removing stains or deposits of hard surfaces.
- the agent according to the invention can also be used industrially to remove deposits, for example of smoke gas resin in boiler plants and combustion chambers.
- the agent according to the invention can also be used to remove impurities on semiconductor surfaces. The use in Etching- method is possible. Another application is the removal of moss.
- Acid agents which are intended in particular to remove stains on textiles in the underarm area are described in WO 2011/077144 A1. known. These agents are highly acidic (pH ⁇ 1) and include, besides an acid, water and a surfactant. If desired, the agent may still be thickened with a gelling agent or a thickener such as ethoxylated fatty alcohols / ethoxylated fatty amines.
- Acid-containing agents for cleaning hard surfaces are known from WO 2009/085049.
- the local agents include an organic acid, nonionic surfactants, water and a hydrophilic polymer which adsorbs to the hard surface.
- hydrophilic polymers that also adsorb to the hard surface this document teaches the use of polybetaines.
- WO 03/066797 teaches a stain remover, which i.a. a hydrophobic component.
- EP 0 786 514 A2 discloses a stain remover which contains nonionic surfactants, anionic soaps and a polymer.
- DE 199 35 259 A1 discloses a bleaching composition which can be used as a pre-treatment or after-treatment agent for textiles.
- the object of the invention is to provide an agent which is suitable for the effective removal of stains and deposits on textiles, especially in the underarm area, and for the removal of the above "difficult" stains and at the same time little or no damage to the surface to be treated becomes.
- a further object is to provide an agent which is also suitable for the removal of deposits and stains on hard surfaces, and in particular the removal of resin, grease or oil-containing deposits on an industrial scale and moss.
- the agent also contains surfactants and a coupling agent in addition to the respective active substances such as acids, alkalis, bleaches and / or not bound in a gel organic hydrophobic solvents in which the adhesion promoter is selected from the group of the alkylene-styrene copolymers, the olefin homopolymers or olefin copolymers of two or more olefins, where the polymers may also be hydrogenated and the polyalkylene derivatives are selected.
- the "active substances" generally cause the actual stain removal.
- the adhesion promoters serve to make the agent sticky so that the agent will adhere to the spot or deposit after application and will not flow away or drip off.
- the surfactants contained in the agent cause on the one hand a cleaning effect. In addition, they help to dissolve the hydrophobic coupling agent in the presence of water.
- the primer which is generally hydrophobic, also provides a protective and delaying effect. Water-soluble active substances are only released from the product in the presence of water. Previously, reactive agents are protected in the hydrophobic matrix.
- reactive agents can also be formulated in the hydrophobic matrix without losing the effect within a short time.
- the agent can be formulated to remove a wide variety of stains or deposits.
- the agent contains, in addition to surfactants and the adhesion promoter as the active ingredient, at least 10% by weight of acid.
- Such an agent can be used to remove acid soluble stains.
- Such acidic agents it is possible to use such acidic agents to remove stains such as rust, blood or impurities on calcifications. Since the acidified agent does not attack the fibers, such a stain and debris removal agent is particularly useful on soft, delicate surfaces such as woven, knit, or walkwear, particularly on textiles, carpets, or curtains.
- the surfaces can z. B. of synthetic or natural fibers, natural or artificial leather or plastic.
- inventive set sour agent can of course also be used to remove such stains from hard, insensitive surfaces, such as metal, ceramic, stone, glass, plastic or wood.
- the agent comprises bleach as active ingredient, for example salts of peracids such as perborates, percarbonates, persulfates or Phthalimidoperoxohexanklare (PAP).
- the bleaching agents are contained in the composition in a concentration of at least 5% by weight and preferably at least 8% by weight and more preferably at least 12% by weight.
- the agent may also contain a bleach activator such as tetrahydrofuran.
- TAED raacetylenethylenediamine
- NOBS nonanoyloxobenzene sulfonate
- DOBS docanoyloxobenzene sulfonate
- the agent comprising bleach comprises at least 20% by weight of surfactants, at least 10% by weight of bleaching agent and between 20% by weight and 60% by weight of adhesion promoter as pure substance or as a solution in a hydrophobic solvent and, if appropriate, bleach activators and solubilizers, In a particularly preferred embodiment, between 25% by weight and 40% by weight of surfactants, at least 10% by weight of peroxoacids and between 30% by weight and 50% by weight of adhesion promoters, in particular alkylene-styrene copolymers dissolved in hydrophobic solvents (Versagel).
- Such agents are suitable for removing red wine, coffee or tea stains from soft sensitive surfaces such as textiles and carpets, but also for removing red wine, coffee or tea stains from the aforementioned hard surfaces.
- the agent is applied to the spot of the object in question, if necessary. Waiting or action times are met, and then washed the object, for example, in a washing machine or rinsed. In the presence of the water, the bleaches and surfactants are then gradually released from the agent at the stain and bleach the stain and transport the contaminants to the wash liquor. Since the active ingredients are enclosed in the hydrophobic matrix of the adhesion promoter and only dissolved in the presence of water from this, overdoses of the active ingredients and thus damage to the tissue can be avoided.
- inventive composition for the removal of fat-soluble and / or pigment-containing impurities such as lipstick, shoe polish, cocoa, fats or waxes can be formulated.
- the agent comprises a hydrophobic organic solvent which serves to dissolve the fats or waxes.
- the hydrophobic organic solvents used for this purpose must thus be freely available in the agent. solu- However, semides which are contained in the composition but which are required for gelation, such as, for example, the hydrophobic solvents which act as solvents for gelation in the bond particularly preferred as adhesion promoter, are not freely available organic solvents in the sense of the invention ,
- Hydrophobic organic solvents for example terpenes, alkanes, mineral oils, long-chain alcohols (R> 10), esters or ethers, are therefore preferably additionally added to the agent via the hydrophobic solvent required for gelation.
- the concentration of the free organic solvents in the composition is at least 10% by weight, preferably above 15% by weight, and more preferably between 20% by weight and 40% by weight.
- the agent should still contain alkalis, which on the one hand also serve to dissolve the fats and oils.
- the alkalis also cause the fibers to swell and thus also facilitate that the active ingredients penetrate sufficiently into the textiles and dissolved impurities can be removed again as a result of the structured structure.
- the concentration of alkalis in such agents is generally at least 2% by weight and preferably at least 5% by weight.
- Such alkalized agents with at least 2% by weight alkali, preferably NaOH or KOH, at least 20% by weight free hydrophobic organic solvent, preferably terpenes, at least 10% by weight adhesion promoter (preferably alkylene styrene copolymer, dissolved in organic solvents such as Versagel) and At least 20% by weight of surfactants are suitable for removing stains containing grease and / or pigment such as cocoa, lipstick, shoe polish, chewing gum and turmeric, preferably of soft, sensitive, in particular textile surfaces. Of course, such an agent can also be used to remove stains from hard surfaces.
- alkali preferably NaOH or KOH
- free hydrophobic organic solvent preferably terpenes
- adhesion promoter preferably alkylene styrene copolymer, dissolved in organic solvents such as Versagel
- surfactants are suitable for removing stains containing grease and / or pigment such as cocoa, lipstick, shoe polish, chewing gum and turmeric, preferably of soft
- the agent is formulated with a very high proportion of alkalis, which is generally above 50% by weight and preferably above 60% by weight.
- alkalis such adhesive, pasty, strongly alkaline agents stick to vertical surfaces and, in the presence of water, for example, by rinsing, release the alkalis, which then deposits of resins, fats, oils or the like. attack.
- Such agents can be used, for example, in industrial plants and combustion chambers to remove fumes, fats or oily impurities or soot.
- Such a highly alkaline agent shows very good results in removing resin or grease deposits even on vertical surfaces (e.g., in slaughterhouses, in pipe-plugging of fats (drain-opener), for removal of keratinous substances (hair, horn)).
- vertical surfaces e.g., in slaughterhouses, in pipe-plugging of fats (drain-opener), for removal of keratinous substances (hair, horn)
- keratinous substances hair, horn
- such a strongly alkaline agent is only suitable in exceptional cases, e.g. for fabrics made of alkali-resistant fibers such as Teflon or PUR.
- composition according to the invention comprises surfactants, it being possible to use anionic, cationic, nonionic and amphoteric surfactants as surfactants.
- surfactants are not only used in the compositions according to the invention for cleaning but also cause the polymer adhering to the surface to be rinsed off again.
- surfactants have a thickening effect on the polymers, i. By adding surfactants, especially in powder form, it is also possible to adjust the viscosity of the agent.
- surfactants it is possible in principle to use all known anionic and / or cationic and / or nonionic and / or amphoteric surfactants, powdery to highlypasteose being preferred.
- the proportion of surfactant in the composition can be up to 80% by weight, preferably 10% by weight to 60% by weight and more preferably 25% by weight to 45% by weight.
- the anionic surfactants perform several tasks in the present invention. First, they serve to emulsify the polymeric matrix without completely destroying the adhesiveness.
- anionic surfactants it is preferred to use one or more substances from the group of the salts of the carboxylic acids, the sulfuric monoesters and the sulfonic acids, preferably from the group of fatty acids, fatty alkyl sulfuric acids and alkylaryl sulfonic acids.
- the C chain distributions of the anionic surfactants are in the range of 6 to 40, preferably 8 to 30 and especially 12 to 22 carbon atoms.
- Carboxylic acids (C6-C22) in the form of their metal salts (preferably alkali metal salts) and their natural or synthetic mixtures and alkali metal salts of sulfuric monoesters and longer-chain alcohols can also be used as anionic surfactants.
- alkyl ether sulfuric acids are synthesized from fatty alcohols which are reacted with ethylene oxide to give the fatty alcohol ethoxylates concerned. Instead of ethylene oxide, propylene oxide can also be used. The subsequent sulfonation provides the relevant alkyl ether sulfuric acids.
- alkali metal salts of alkanesulfonic acids and olefinsulfonic acids can also be used as anionic surfactants in the context of the present invention.
- Alkanesulfonic acids may contain the sulfonic acid group terminally bound (primary alkanesulfonic acids) or along the C chain (secondary alkanesulfonic acids).
- Typical representatives are alkylbenzenesulfonates, particularly preferably linear alkylbenzenesulfonates (LAS).
- LAS linear alkylbenzenesulfonates
- the above-mentioned anionic surfactants may be used in their neutralized form alone or in admixture with each other.
- the surfactant phase contains, based on its weight, preferably 10% by weight to 90% by weight and particularly preferably 40% by weight to 85% by weight of lauryl sulfate.
- nonionic surfactants it is possible to use alkoxylated, preferably ethoxylated, in particular primary, alcohols having preferably 8 to 18 carbon atoms and on average 1 to 12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol radical can be linear or preferably methyl-branched in the 2-position or linear and methyl-branched radicals in the mixture can contain, as they are usually present in Oxoalkoholresten.
- fatty alcohols with more than 12 EO. Examples include tallow fatty alcohol with 14 EO, 25 EO, 30 EO or 40 EO.
- alkyl-O (G)
- alkyl is a primary straight-chain or methyl-branched, especially methyl-branched in the 2-position aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G is the symbol for a glycosidic structure with 5 or 6 C atoms, preferably for glucose.
- nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably having from 1 to 4 carbon atoms in the alkyl chain, especially fatty acid methyl esters.
- Nonionic surfactants of the amine oxide type for example N-cocoalkyl-N, N-dimethylamine oxide and N-tallowalkyl-N, N-dihydroxyethylamine oxide or alkanolamides can also be used.
- the proportion of the nonionic surfactant or surfactants in the total surfactant phase can be up to 50%, preferably up to 30% and particularly preferably up to 25%.
- the surfactant phase can also be provided with cationic or amphoteric and zwitterionic surfactants.
- amphoteric surfactants are fatty acid amidopropyl betaines with C5-C21 fatty acid moieties, but also amphodiacetates.
- Cationic surfactants are preferably used in the present acidic formulation as bactericidal substances.
- Zwitterionic surfactants can be described by way of example as quaternary ammonium, phosphonium or sulfonium components which are connected via an aliphatic bridge with another now anionic group such as Carbboxy, sulfonate, sulfate, phosphate or phosphonate.
- foaming agent olefin sulfonates, ether sulfates or acid methyl taurides can furthermore be added to the agent.
- strong foaming agents preferably 1 to 50, in particular 1 to 25%, of the surfactant phase can be obtained by one or more frothers, e.g. from the group of betaines, the alkoxylated alkyl ether sulfates or Lactobi- onklarivate be replaced.
- foaming agents may be selected from fatty acid amidopropyl betaines having a C 5 -C 21 fatty acid moiety, such as cocoamido proplybetaine, the alkali metal or ammonium salts of the lauryl ether sulfates containing 1 to 5 EO, the lactobionococoylamide, the lactobionooleylamide, the lactobionotalgamide, etc., or mixtures thereof.
- foaming agents can be incorporated well into the composition according to the invention. Preference is given to using such cosurfactants which are present in solid, preferably pulverulent or highly viscous form.
- adhesion promoters which are selected from a group of the alkylene styrene copolymers, the olefin homopolymers or olefin copolymers of two or more olefins, where the polymers may also be hydrogenated, and the polyalkylene derivatives.
- Preferred alkylene-styrene copolymers are diblock or tri-block copolymers, in particular from the group consisting of styrene-butadiene-styrene copolymers (SBS), styrene-isoprene-styrene copolymer (SIS) and styrene-ethylene-butylene-styrene Copolymers (S-EB-S), styrene-ethylene-propylene copolymers (S-EP), styrene-ethylene-butylene copolymers (S-EB), styrene-butadiene copolymers (SB) and styrene-isoprene copolymers ( SI).
- the alkylene styrene copolymers may also be hydrogenated or partially hydrogenated.
- the hydrogenated or non-hydrogenated alkylene-styrene copolymers are crosslinked.
- the alkylene styrene copolymers are preferably dissolved in a solvent, in particular hydrophobic solvents such as mineral or vegetable oils, alkanes or aromatic hydrocarbons.
- a solvent in particular hydrophobic solvents such as mineral or vegetable oils, alkanes or aromatic hydrocarbons.
- the solvents should be aprotic and non-polar and preferably inert.
- Such gels generally consist of about 1 to 20% by weight of polymers and 80 to 99% by weight of hydrophobic solvents, such as, for example, mineral oil.
- Alkylene-styrene copolymers are offered, for example, in the form of a solution in a hydrophobic solvent from Penreco under the trade name Versagel, such as the Versagel M750 or the Versagel M1600.
- Versagel such as the Versagel M750 or the Versagel M1600.
- Kraton Performance Polymers offers alkylene-styrene copolymers as a solid under the trademark "Kraton”.
- the agents are also sticky. This ensures that the agent adheres to the surface of the object in question and can thus act on the surface to be treated during the rinse or during the washing process over a longer period of time.
- olefin homopolymers or copolymers can be used polybutadiene rubbers, styrene-butadiene block and copolymers and the polyisopropenes, but also random (block) polymers, which are obtained by 1,3-addition of butadiene or isoprene to styrene or alpha-methylstyrene , Homopolymers or copolymers of ethylene or propylene, such as ethylene-propylene-diene terpolymers, which are natural The rubbers and the norbornene polymers or polydicyclopentadiene can be used.
- the compounds from the group of olefin homopolymers and copolymers can also be partially hydrogenated, partially oxidized or further functionalized via graft molecules.
- Another possible class of adhesion promoters from the group of polyalkylene derivatives comprises polyalkylene chains with randomly distributed functional groups.
- the polyalkylene chains are preferably polybutadiene, polyisopropylene and polypropylene chains.
- the randomly distributed on the polyalkylene functional groups are preferably reactive groups, in particular from the group of anhydrides, thiols, epoxides or primary amines.
- the functional groups should be selected so that the coupling agents do not react with the other components of the agent.
- polymers having randomly attached to the polybutadiene chain maleic anhydride groups Particular preference is given to polymers having randomly attached to the polybutadiene chain maleic anhydride groups.
- the particularly preferred maleic anhydride adduct on 1,4-cis-polybutadiene is available from Degussa under the name Polyvest.
- the agent according to the invention furthermore contains at least one active substance which is to be selected according to the stain to be removed or the deposit to be removed.
- Active substances for the purposes of the present invention are acids, alkalis, bleaches and freely available organic hydrophobic solvents.
- the agent may also contain a plurality of active substances.
- the agent according to the invention contains acids as active substance
- the agent is suitable, for example, for removing stains from soft surfaces, such as stains of clothing pieces in the underarm area or rust and blood stains or impurities on calcifications.
- acids organic and inorganic acids, also in combination, can be used.
- organic acids examples include acetic acid, lactic acid, citric acid, levulinic acid, tartaric acid, formic acid, glycolic acid, succinic acid, glutaric acid, maleic acid, methanesulfonic acid, sulfamic acid or else oxalic acid.
- concentration of organic acids should be between 1% by weight and 60% by weight, preferably between
- inorganic acids for example, sulfuric acid, nitric acid, hydrochloric acid or phosphoric acid can be used.
- concentration of inorganic acids in the composition should be between 1% and 40% by weight, preferably between 10% and 30% by weight, at an acidified level.
- the minimum content of acids (organic and / or inorganic) in the composition should be at least 10% by weight.
- the pH of a 1% solution of the agent with an acid should be pH 2 or less, preferably at most pH 1.5, and most preferably at most pH 1.
- the agent as active substance in addition to the at least one acid comprises at least one oxidizing agent.
- Such a variant is suitable for removing stains from rust, blood, sweat and oxidizable substances.
- phosphoric acid can be used with H2O2 (stabilized).
- the proportion of H2O2 (absolute) in the agent should preferably be between 2% by weight and 5% by weight.
- an agent comprising a high proportion of alkalis is suitable.
- alkalis for example, oxides and hydroxides of alkali and alkaline earth metals such as NaOH, KOH or MgO or Na2Ü, preferably as a solid or prills, can be used.
- the proportion of alkalis in the composition can be any proportion of alkalis in the composition.
- the pH of a 1% solution of an alkaline admixed agent should be at least pH 9, preferably at least pH 10 and more preferably at least pH 11.
- an agent that comprises alkalis and free hydrophobic organic solvents as the active substance is suitable.
- the alkalis serve to swell the fibers.
- Alkalis and hydrophobic solvents serve to dissolve and / or chemically modify the fat-soluble impurities, e.g. by ester cleavage.
- the adhesion promoter in a hydrophobic solvent such as a mineral oil is gelelt (eg as Versagel 1600) and the part of the mineral oil, which is required for the gel formation is not available as a hydrophobic solvent, the dissolution of fat-soluble Substances in the recipe only by "free", that is, not required for gelation solvents occur.
- the mineral oil-containing Versagel required for gelation in the agent still additional hydrophobic solvents such as terpenes in a proportion - depending on the stain to be removed - of at least 10 wt.% And preferably up to 40 wt.% given.
- the proportion of alkalis is at least 2% by weight.
- the free hydrophobic solvents cause already when applying the agent on the stain a dissolving oil-containing contamination.
- inventive agent as
- Active substance alkalies and bleach include.
- bleaching agents which are stable in the alkaline such as chlorine-releasing bleaching agents such as cyanurates or chlorine bleaches, preferably in a concentration of 0.01 wt.% To 1 wt.% Additionally added to the agent described above with alkalis as active substance.
- Such an agent is useful for removing stains from fabrics that are chlorine stable, preferably undyed fibers.
- composition according to the invention may additionally comprise solubilizers in order to facilitate the emulsification via phase boundaries.
- solubilizers for example, glycol ethers or sodium cumene sulfonate can be used, preferably in a concentration between 1 wt.% And 40 wt.%.
- agent according to the invention may also comprise humectants.
- humectants Preferably, polyalcohols such. As glycerol or glycol used.
- co-thickeners may be added to the composition according to the invention in order to increase the plasticity of the composition.
- co-thickeners may include, for example, bentonites, powder surfactants, xanthans, polybutadiene rubbers, polyisopropenes, block copolymers comprising linked oligomers consisting of oligo- or polyethylene oxide and / or oligo- or propylene oxide and / or oligo- or polybutylene oxide and also arylethoxylates or alkyl-aryl-ethoxylates become.
- the polymeric natural substances such as lignins or their alkali metal or alkaline earth metal salts can also be used as (co) thickeners.
- Sequestering agents such as sodium diphosphonate, useful, for example, to remove tea stains may also be added to the composition.
- dispersants that hold, for example, Ca or Mg salts in the wash liquor in suspension, may be included in the composition as a component.
- the agent may also include complexing agents such as phosphonates or EDTA.
- hydrophobicizers such as, for example, Aerosil, in particular methylated Aerosil (Carobo Carbon) can be added to the composition according to the invention as fillers.
- agent according to the invention - if desired - also include dyes, fragrances and enzymes (amylases, lipases, proteases, cellulases and peroxidases).
- the agent may further contain odoriferous agents (malodor counteractants) which are preferably added to the fragrances.
- odoriferous agents malodor counteractants
- Such odor binders are described, for example, in US Pat. No. 7,288,507 B2.
- the viscosity of the agent can be adjusted depending on the desired application and the type of application.
- the viscosity of the agent should on the one hand be so low that the agent can effectively wet the spot to be treated. On the other hand, the viscosity of the agent should again be so high that it does not "run away" from the spot or the contaminant to be treated and the amount applied can be metered.
- the agents can be thin to viscous, depending on which type of surface or fabric they are applied and which should adhere for a relatively long time.
- the agent according to the invention is preferably pasty.
- the composition has a viscosity of at least 30 Pa * s, in particular at least 100 Pa * s, measured with a Haake viscometer, system plate / plate, plate diameter 10 mm, with a shear rate of 2.62 s-1 and 20 ° C on.
- a paste can for example be painted on the surface to be treated by means of a brush or a spatula, where it adheres.
- the stain remover according to the invention is applied to the point to be cleaned of the object to be treated, in particular the textiles, on the stain or in the underarm area with brush or brush.
- the stain remover sticks and slowly releases in the presence of water then in the alkaline wash the active ingredients that gradually dissolve the stain.
- composition according to the invention is generally suitable for removing stains from textiles of plant, animal or synthetic origin.
- the deodorant removal agent is suitable for removing sweat from cotton textiles.
- the stain remover according to the invention is first applied to the stain to be removed, where it adheres.
- the applied stain remover is removed again, for example, by washing the treated garment after a certain exposure time of at least one minute in the washing machine or even by hand.
- the water-soluble active substance ie the alkalis or the bleaching agent
- the stain is removed locally in the vicinity of the stain and the stain is removed.
- the rest of the "non-stained" material, especially textiles, is mainly affected by the washing liquor or - if no washing is done in the washing machine with a detergent - water.
- the stain remover Upon contact with water, the stain remover is completely removed from the surface, also as a result of the surfactants contained in the composition.
- composition according to the invention can also be used to remove blood, rust and iron stains or other acid-soluble stains.
- composition according to the invention can also be used for removing moss and other deposits, for example on stones.
- benzalkonium chloride bronopol, glutaraldehyde, formaldehyde, triazine, dibromonitrilepropionamide, perbutryn, IPBC, OIT and diuron can be used as the biocide.
- the agent can also be used to remove impurities from copper or other metals on hard surfaces such as circuit boards.
- the stain remover according to the invention is preferably applied to the object to be treated at room temperature and then rinsed off again with cold or warm water.
- the agent according to the invention is particularly suitable for single use for the removal of stains and impurities, the entire agent subsequently being removed again with water after application.
- the agent should preferably be anhydrous or a water content of at most 5 wt % and more preferably at most 1% by weight.
- a frame formulation and an example formulation for an acid agent according to the invention are shown, which can serve, for example, for removing stains on textiles in the underarm area.
- the Armpit Cleaner according to Formulation II above was applied to patches of a blue multiply worn T-shirt in the underarm area. On the adjacent stain in the armpit was Dr. med. Beckmann's spot devil "rust &deodorant" applied according to instructions.
- the washing conditions were as follows: 55 g washing powder to 4.5 kg laundry, liquor ratio 1: 5, washing temperature 40 ° C, 250 mg / cm 2 Armpit Cieaner, exposure time 60 minutes, washing time 30 minutes, washout 3 x 30 seconds, cold ,
- Figure 1 shows the starting material with the stains in the armpit area and the result after removal of the stain the armpit Cieaner invention and with Dr. med. Beckmann's spot devil.
- CA acetate
- CO cotton
- PA polyamide
- PAN polyacrylic
- PES polyester
- WO wool
- each test material was washed separately. The samples thus obtained were used for the further tests.
- the tensile properties of the textile fabrics were determined in accordance with DIN EN ISO 13934-1, determination of the maximum tensile force and maximum tensile force elongation with the strip tensile test, issuing date: 1999-04 with clamping length 200 mm, strip width: 50 mm, test speed (chain) 100 mm / min, test speed (shot): 100 mm / min, preload force 2 N.
- the following recipe is particularly suitable for removing the above stains on soft surfaces such as textiles.
- Lutensol AO 5 (C13 / C15 oxo alcohol ethoxylate / 5 EO, BASF) 5
- Lutensol AO 8 (C13 / C15 oxo alcohol ethoxylate / 8 EO, BASF) 15
- Sokalan PA30 CL polyacrylate, BASF
- Texapon SPN 70 sodium lauryl ether sulfate, Cognis
- the NaOH contained in the agent acts as a grease and causes a swelling of the fibers, so that the ingredients can get better to the fiber and be transported away from it again.
- the following acidic agent may be used:
- This formulation includes as sodium bleach sodium perborate and TAED as oxidation activator.
- FIG. 4 shows the removal of red wine stains with the composition according to the invention in accordance with recipe X and for comparison with Dr. med. Beckmann's tainted devil "Fruits & Beverages.”
- the illustrations show that the stain with the composition according to Formulation X is completely removed in a single treatment, compared to Dr. Beckmann's tainted devil d) Lipstick stains
- the stain paste of the invention is applied evenly to the stain with the spatula.
- the exposure time is 15 to 30 minutes.
- Dr. Beckmann's patch devil is applied according to instructions.
- the laundry was carried out as follows in the concentration ratio: 55 g of washing powder to 4.5 kg of laundry, liquor ratio 1: 5, washing temperature 40 ° C, ballast wash (BW terry).
- washing process in a washing machine washing program 40 ° C without prewash.
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- Chemical & Material Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Dispersion Chemistry (AREA)
- Detergent Compositions (AREA)
- Paints Or Removers (AREA)
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Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE102013106363.2A DE102013106363B3 (de) | 2013-06-18 | 2013-06-18 | Mittel zur Entfernung von Flecken und Ablagerungen |
PCT/EP2014/062799 WO2014202651A1 (de) | 2013-06-18 | 2014-06-18 | Mittel zur entfernung von flecken und ablagerungen |
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EP3011002A1 true EP3011002A1 (de) | 2016-04-27 |
EP3011002B1 EP3011002B1 (de) | 2020-01-08 |
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EP14731263.1A Active EP3011002B1 (de) | 2013-06-18 | 2014-06-18 | Mittel zur entfernung von flecken und ablagerungen |
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US (1) | US10047322B2 (de) |
EP (1) | EP3011002B1 (de) |
JP (1) | JP2016533412A (de) |
KR (1) | KR20160021773A (de) |
CN (1) | CN105324474B (de) |
AU (1) | AU2014283324B2 (de) |
BR (1) | BR112015030856A2 (de) |
CA (1) | CA2913638C (de) |
DE (1) | DE102013106363B3 (de) |
MX (1) | MX2015017226A (de) |
MY (1) | MY171321A (de) |
NZ (1) | NZ716097A (de) |
PH (1) | PH12015502696A1 (de) |
SG (1) | SG11201509718VA (de) |
WO (1) | WO2014202651A1 (de) |
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EP3847229B1 (de) * | 2018-09-05 | 2023-07-05 | Unilever Global Ip Limited | Schäumbare reinigungszusammensetzung |
US20200157476A1 (en) * | 2018-11-16 | 2020-05-21 | The Procter & Gamble Company | Composition and method for removing stains from fabrics |
CN111518600B (zh) * | 2019-12-23 | 2021-05-18 | 新疆中宇金盾碳基研究院(有限公司) | 泛碱抑制剂、含有泛碱抑制剂的兰炭基型碳及其制备方法 |
EP4247926A1 (de) * | 2020-11-17 | 2023-09-27 | Unilever IP Holdings B.V. | Zusammensetzung |
CN113122396A (zh) * | 2021-03-12 | 2021-07-16 | 大连传奇化工有限公司 | 一种织物表面卟啉及共轭双键结构类污渍去除剂及其制备方法 |
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-
2013
- 2013-06-18 DE DE102013106363.2A patent/DE102013106363B3/de not_active Withdrawn - After Issue
-
2014
- 2014-06-18 CN CN201480035087.4A patent/CN105324474B/zh not_active Expired - Fee Related
- 2014-06-18 AU AU2014283324A patent/AU2014283324B2/en not_active Ceased
- 2014-06-18 KR KR1020157035175A patent/KR20160021773A/ko not_active Application Discontinuation
- 2014-06-18 WO PCT/EP2014/062799 patent/WO2014202651A1/de active Application Filing
- 2014-06-18 JP JP2016520459A patent/JP2016533412A/ja active Pending
- 2014-06-18 BR BR112015030856A patent/BR112015030856A2/pt not_active IP Right Cessation
- 2014-06-18 CA CA2913638A patent/CA2913638C/en not_active Expired - Fee Related
- 2014-06-18 MX MX2015017226A patent/MX2015017226A/es unknown
- 2014-06-18 SG SG11201509718VA patent/SG11201509718VA/en unknown
- 2014-06-18 NZ NZ716097A patent/NZ716097A/en not_active IP Right Cessation
- 2014-06-18 MY MYPI2015704524A patent/MY171321A/en unknown
- 2014-06-18 EP EP14731263.1A patent/EP3011002B1/de active Active
- 2014-06-18 US US14/899,983 patent/US10047322B2/en not_active Expired - Fee Related
-
2015
- 2015-12-03 PH PH12015502696A patent/PH12015502696A1/en unknown
Non-Patent Citations (1)
Title |
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See references of WO2014202651A1 * |
Also Published As
Publication number | Publication date |
---|---|
CA2913638A1 (en) | 2014-12-24 |
AU2014283324A1 (en) | 2016-02-11 |
US10047322B2 (en) | 2018-08-14 |
MY171321A (en) | 2019-10-09 |
JP2016533412A (ja) | 2016-10-27 |
US20160137955A1 (en) | 2016-05-19 |
MX2015017226A (es) | 2016-11-10 |
PH12015502696B1 (en) | 2016-03-14 |
SG11201509718VA (en) | 2015-12-30 |
NZ716097A (en) | 2017-07-28 |
AU2014283324B2 (en) | 2017-04-06 |
BR112015030856A2 (pt) | 2017-07-25 |
PH12015502696A1 (en) | 2016-03-14 |
EP3011002B1 (de) | 2020-01-08 |
CN105324474B (zh) | 2019-09-13 |
DE102013106363B3 (de) | 2014-12-11 |
KR20160021773A (ko) | 2016-02-26 |
WO2014202651A1 (de) | 2014-12-24 |
CN105324474A (zh) | 2016-02-10 |
CA2913638C (en) | 2018-11-20 |
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