EP1791936A1 - Reinigungsformulierungen für die maschinelle geschirrreinigung enthaltend hydrophob modifizierte polycarboxylate - Google Patents
Reinigungsformulierungen für die maschinelle geschirrreinigung enthaltend hydrophob modifizierte polycarboxylateInfo
- Publication number
- EP1791936A1 EP1791936A1 EP05782771A EP05782771A EP1791936A1 EP 1791936 A1 EP1791936 A1 EP 1791936A1 EP 05782771 A EP05782771 A EP 05782771A EP 05782771 A EP05782771 A EP 05782771A EP 1791936 A1 EP1791936 A1 EP 1791936A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- weight
- carbon atoms
- group
- monomer
- 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
Classifications
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/33—Amino carboxylic acids
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- 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
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- 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
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
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- 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
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
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- 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
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
Definitions
- the invention relates to cleaning formulations for machine dishwashing.
- the dishes are freed of dirt, which consists of a wide variety of food residues, which also contain fatty and oily components, during the cleaning process.
- the detached dirt particles and components are pumped during further cleaning in the rinse water of the machine. It must be ensured that the detached Schmutz ⁇ particles are well dispersed and emulsified, so they do not settle on the dishes again.
- phosphate-based Many of the formulations on the market are phosphate-based.
- the phosphate used is ideal for use because it combines many useful properties that are needed in machine dishwashing.
- phosphate is able to disperse water hardness (i.e., insoluble salts of water hardness causing ions such as calcium and magnesium ions). This task is still achieved via the ion exchanger of the machines.
- water hardness i.e., insoluble salts of water hardness causing ions such as calcium and magnesium ions
- This task is still achieved via the ion exchanger of the machines.
- a large proportion of the products for automatic dishwashing is currently available in the form of so-called 3-in-1 formulations, in which the function of the ion exchanger is no longer necessary.
- the phosphate usually takes over the softening of the water in combination with phosphonates. Furthermore, the phosphate disperses the detached dirt and thus prevents re-deposition of the dirt on the dishes.
- the object of the invention is to provide phosphate-free cleaning formulations for machine dishwashing.
- the object of the invention is, in particular, to provide such formulations which, without the use of additional rinse aid, result in a dish-free, covering-free and drip-free dish.
- the complexing agent takes on the task of complexing the water hardness causing ions (calcium and magnesium ions), which are contained in the rinse water or the Suite ⁇ .
- Polycarboxylates likewise have a calcium dispersancy and, in addition, are also able to disperse the soil present in the wash liquor.
- particularly hydrophobically modified polycarboxylates have proven to be advantageous. It is believed that the hydrophobic side chains are able to interact with hydrophobic soil constituents such as oils and fats.
- phosphate-free cleaning formulations for machine dishwashing containing as components: a) 1 to 20 wt .-% of copolymers
- a1 from 20 to 80% by weight, preferably from 30 to 70% by weight, of at least one monomer from the group consisting of monoethylenically unsaturated C 3 -C 10 -mono- or dicarboxylic acids or their anhydrides,
- R 1 , R 2 and R 3 independently of one another, denote H, CH 3 or C 2 H 5 , R 4 signifies a linear, branched or cyclic radical having 1 to 6 carbon atoms or an aromatic radical having 6 to 12 carbon atoms,
- complexing agents selected from the group consisting of nitrilotriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, hydroxyethylethylenediaminetriacetic acid and methylglycinediacetic acid, glutamic diacetic acid, iminodisuccinic acid, hydroxyiminodisuccinic acid, ethylenediamine disuccin
- g 0 to 50% by weight, preferably 0.1 to 50% by weight, of one or more further additives such as anionic or zwitterionic surfactants, bleach catalysts, alkali carriers, corrosion inhibitors, defoamers, dyes, fragrances, fillers, or ⁇ ganic solvents and water,
- further additives such as anionic or zwitterionic surfactants, bleach catalysts, alkali carriers, corrosion inhibitors, defoamers, dyes, fragrances, fillers, or ⁇ ganic solvents and water
- the formulation may be processed as a tablet, powder, gel, capsule or solution. These may be formulations for both household and commercial applications.
- the object is further achieved by the use of a combination of copolymers a) and Komplexsentnem b) as a builder system in cleaning formulations for machine ⁇ eschirrgraphy.
- Suitable monomers a1) are, for example, maleic acid, maleic anhydride, acrylic acid, methacrylic acid, fumaric acid, itaconic acid and citraconic acid.
- Preferred copolymers a) contain as monomers a1) monomers which are selected from the group consisting of maleic acid, maleic anhydride and acrylic acid.
- Suitable monomers a2) are, for example, isobutene, diisobutene, butene, pentene, hexene and styrene.
- Further preferred copolymers a) contain as monomers a2) monomers which are selected from the group consisting of isobutene, diisobutene (2-methyl-3,3-dimethyl-1-butene) and styrene.
- Suitable monomers a3) have at least 10, generally 10-26, carbon atoms.
- Suitable monomers a3) are, for example, 1-decene, 1-dodecane, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, 1-docoses, 1-tetracoses and 1-hexacoses.
- copolymers a) comprise as monomers a3) monomers aus ⁇ selected from the group consisting of 1-dodecene, 1-octadecene, C 22 -alpha-olefin, a mixture of C 2 oC 24 -alpha-olefins and polyisobutene with an average of 12 to 100 G atoms.
- Particularly preferred copolymers a) comprise both monomers a1), which are selected from maleic acid, maleic anhydride and acrylic acid, as well as monomers a2) which are selected from isobutene, diisobutene and styrene as well as monomers a3), which are selected from the group consisting of 1 Dodecene, 1-octadecene, C 22 -alpha-olefin, a mixture of C 2 oC 24 -alpha-olefins and polyisobutene having an average of 12 to 100 carbon atoms.
- copolymers of 30 to 70% by weight of maleic acid and maleic anhydride as monomers a1), 20 to 40% by weight of isobutene as monomers a2) and 5 to 20% by weight of octadecene as monomers a3).
- the cleaning formulations according to the invention comprise one or more complexing agents selected from the group consisting of nitrilotriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, hydroxyethylethylenediaminetriacetic acid and methylglycinediacetic acid, glutamic acid diacetic acid, iminodisuccinic acid, hydroxyiminodisuccinic acid, ethylenediaminedicarboxylic acid, aspartic acid diacetic acid and salts thereof.
- Preferred complexing agents b) are methylglycinediacetic acid and its salts.
- the cleaning formulations according to the invention contain weakly or low-foaming nonionic surfactants. These are generally present in proportions of 0.1 to 20 wt .-%, preferably 0.1 to 15 wt .-%, particularly preferably 0.25 to 10 wt .-%.
- Suitable nonionic surfactants include the surfactants of the general formula (II)
- R 2 is a linear or branched alkyl radical having 8 to 22 carbon atoms
- R 1 and R 3 are independently hydrogen or a linear or branched alkyl radical having 1-10 C atoms or H, wherein R 1 is preferably methyl
- p and m are independently 0 to 300.
- the surfactants of formula (II) may be both random copolymers and block copolymers, preferably block copolymers.
- the formulations may further contain anionic or zwitterionic surfactants, preferably in admixture with nonionic surfactants. Suitable anionic and zwitterionic surfactants are likewise mentioned in EP-A 851 023 and DE-A 198 19 187.
- the cleaning formulations according to the invention comprise bleaches and optionally bleach activators.
- Bleaching agents are subdivided into oxygen bleaching agents and chlorine-containing bleaching agents.
- Use as oxygen bleach find alkali metal perborates and their hydrates and Alkaiimetallpercarbonate.
- Preferred bleaches are sodium perborate in the form of the mono- or tetrahydrate, sodium percarbonate or the hydrates of sodium percarbonate.
- oxygen bleaching agents are persulfates and hydrogen peroxide.
- Typical oxygen bleaches are also organic peracids such as perbenzoic acid, peroxy-alpha-naphthoic acid, peroxylauric acid, peroxystearic acid, phthalimidoperoxycaproic acid, 1,12-diperoxydodecanedioic acid, 1,9-diperoxazelainic acid, diperoxoisophthalic acid or 2-decyldiperoxybutan-1, 4- dioic.
- organic peracids such as perbenzoic acid, peroxy-alpha-naphthoic acid, peroxylauric acid, peroxystearic acid, phthalimidoperoxycaproic acid, 1,12-diperoxydodecanedioic acid, 1,9-diperoxazelainic acid, diperoxoisophthalic acid or 2-decyldiperoxybutan-1, 4- dioic.
- oxygen bleaches can also be used in the detergent formulation:
- Oxygen bleaching agents are used in amounts of generally from 0.5 to 30% by weight, preferably from 1 to 20% by weight, particularly preferably from 3 to 15% by weight, based on the total detergent formulation.
- Chlorine-containing bleaches as well as the combination of chlorine-containing bleach with peroxide-containing bleaches may also be used.
- Known chlorine-containing bleaching agents are, for example, 1,3-dichloro-5,5-dimethylhydantoin, N-chlorosulfamide, chloramine T, dichloramine T, chloramine B, N, N'-dichlorobenzoylurea, p-toluenesulfondichloroamide or trichloroethylamine.
- Preferred chlorine-containing bleaching agents are sodium hypochlorite, calcium hypochlorite, potassium hypochlorite, magnesium hypochlorite, potassium dichloroisocyanurate or sodium dichloroisocyanurate.
- Chlorine-containing bleaching agents are used in amounts of generally from 0.1 to 20% by weight, preferably from 0.2 to 10% by weight, particularly preferably from 0.3 to 8% by weight, based on the total detergent formulation used.
- bleach stabilizers such as, for example, phosphonates, borates, metaborates, metasilicates or magnesium salts can be added in small amounts.
- Bleach activators are compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 carbon atoms, in particular 2 to 4 carbon atoms, and / or substituted perbenzoic acid. Suitable compounds are those which contain one or more N- or O-acyl groups and / or optionally substituted benzoyl groups, for example substances from the class of the anhydrides, esters, imides, acylated imidazoles or oximes.
- TAED tetraacetylethylenediamine
- TAMD tetraacetylmethylenediamine
- TA-GU tetraacetylglycoluril
- TAHD tetraacetylhexylenediamine
- N-acylimides such as N-nonanoylsuccinimide (NOSI)
- acylated phenolsulphonates such as n-nonanoyl or isononanoyloxybenzenesulphonates (n- or iso-NOBS)
- PAG pentaacetylglucose
- DADHT 1, 5-diacetyl-2,2-dioxohexahydro-1,3,5-triazine
- ISA isatoic anhydride
- bleach activators are also suitable as bleach activators are nitrile quats such as N-methyl morpholinium acetonitrile salts (MMA salts) or trimethyl am
- Bleach activators are preferably suitable from the group consisting of multiply acylated alkylenediamines, more preferably TAED, N-acylimides, more preferably NOSI, acylated phenolsulfonates, particularly preferably n- or iso-NOBS, MMA and TMAQ.
- Carboxylic acid anhydrides such as phthalic anhydride; acylated polyhydric alcohols such as triacetin, ethylene glycol diacetate or 2,5-diacetoxy-2,5-dihydrofuran; the enol esters known from DE-A 196 16 693 and DE-A 196 16 767 and acetylated sorbitol and mannitol and their mixtures described in EP-A 525 239; acylated sugar derivatives, in particular pentaacetylglucose (PAG), pentaacetylfructose, tetraacetylxylose and octaacetyl lactose, and also acetylated, optionally N-alkylated, glucamine and gluconolactone, and / or N-acylated lactams, for example N-benzoylcaprolactam, which are known from WO 94 27,970, WO
- bleach activators are used in amounts of generally from 0.1 to 10% by weight, preferably from 1 to 9% by weight, particularly preferably from 1.5 to 8% by weight, based on the total cleaner formulation.
- the cleaning formulations of the invention may contain further builders. It is possible to use water-soluble and water-insoluble builders whose main task is the binding of calcium and magnesium.
- carboxylic acids and their salts such as alkali citrates, in particular anhydrous trisodium citrate or trisodium citrate dihydrate, alkali metal succinates, alkali metalates, fatty acid sulfonates, oxydisuccinate, alkyl or alkenyl disuccinates, gluconic acids, oxadiacetates, carboxymethyloxysuccinates, tartrate monosuccinate, tartrate disuccinate,
- Aminopolycarboxylates and polyaspartic acid are Aminopolycarboxylates and polyaspartic acid
- Phosphonates such as 2-phosphono-1, 2,4-butanetricarboxylic acid, aminotri (methylenephosphonic acid), 1-hydroxyethylene (1,1-diphosphonic acid), ethylenediaminetetra methylenephosphonic acid, hexamethylenediamine tetramethylenephosphonic acid or
- Silicates such as sodium disilicate and sodium metasilicate
- water-insoluble builders such as zeolites and crystalline phyllosilicates.
- the cleaning formulations according to the invention contain enzymes.
- the cleaning agent can be added between 0 and 8 wt .-% of enzymes, based on the total preparation, to increase the performance of the detergents or to ensure under mild conditions, the cleaning performance of the same quality.
- the most commonly used enzymes include lipases, amylases, cellulases and proteases.
- esterases pectinases, lactases and peroxidases.
- the cleaning agents according to the invention may contain, as component g), further additives such as anionic or zwitterionic surfactants, bleach catalysts, alkali carriers, corrosion inhibitors, defoamers, dyes, fragrances, fillers, organic solvents and water.
- further additives such as anionic or zwitterionic surfactants, bleach catalysts, alkali carriers, corrosion inhibitors, defoamers, dyes, fragrances, fillers, organic solvents and water.
- the sulfone imines and / or bleach-enhancing transition metal salts or transition metal complexes known from EP-A 446 982 and EP-A 453 003 can also be present as so-called bleach catalysts in the cleaning formulations according to the invention.
- Suitable transition metal compounds include, for example, the manganese, iron, cobalt, ruthenium or molybdenum-salene complexes known from DE-A 195 29 905 and their N-analogues known from DE-A 196 20 267, which consist of DE-A 195 36 082 known manganese, iron, cobalt, ruthenium or molybdenum carbonyl, the described in DE-A 196 05 688 manganese, iron, cobalt, ruthenium, molybdenum, titanium, vanadium and copper complexes with nitrogen-containing tripod ligands, the cobalt, iron, copper and ruthenium-amine complexes known from DE-A 196 20 411, the manganese, copper and titanium compounds described in DE-A 44 16 438 Cobalt complexes, the cobalt complexes described in EP-A 272 030, the manganese complexes known from EP-A 693 550, the manganese, iron, cobal
- Binuclear manganese complexes containing 1, 4,7-trimethyl-i, 4,7-triazacyclononane such as [(TMTACN) 2 Mn lv Mn lv ( ⁇ -O) 3 ] 2+ (PF 6 ") 2 ) are also useful as effective bleach catalysts
- TMTACN 1, 4,7-trimethyl-i, 4,7-triazacyclononane
- Suitable bleach catalysts are preferably bleach-enhancing transition metal complexes or salts from the group consisting of the manganese salts and complexes and the cobalt salts and complexes. Particularly suitable are the cobalt (amine) complexes, the cobalt (acetate) complexes, the cobalt (carbonyl) complexes, the chlorides of cobalt or manganese, manganese sulfate or [(TMTACN) 2 Mn ' v Mn lv ( ⁇ -) O) 3 ] 2+ (PF 6 " ) 2 .
- Bleach catalysts can be used in amounts of from 0.0001 to 5% by weight, preferably from 0.0025 to 1% by weight, particularly preferably from 0.01 to 0.25% by weight, based on the total detergent formulation ,
- alkali carriers may be present. Suitable alkali carriers are ammonium and / or alkali metal hydroxides, ammonium and / or alkali metal carbonates, ammonium and / or alkali metal hydrogencarbonates, ammonium and / or alkali metal sesquicarbonates, ammonium and / or alkali metal silicates, ammonium and / or alkali metal silicates and mixtures of the abovementioned substances. It being preferred to use ammonium and / or alkali metal carbonates, in particular sodium carbonate, sodium bicarbonate or sodium sesquicarbonate.
- silver protectants from the group of the triazoles, the benzotriazoles, the bisbenzotriazoles, the aminotriazoles, the alkylaminotriazoles and the transition metal salts or complexes. Particularly preferred to use are benzotriazole and / or alkylaminotriazole.
- active chlorine-containing agents are often used in cleaner formulations, which can significantly reduce the corrosion of the silver surface.
- Oxygen- and nitrogen-containing organic redox-active compounds such as di- and trihydric phenols, for example hydroquinone, pyrocatechol, hydroxyhydroquinone, gallic acid, phloroglucinol, pyrogallol and derivatives of these classes of compounds are preferably used in chlorine-free cleaners.
- salt and complex inorganic compounds such as salts of the metals Mn, Ti, Zr Hf 1 V, Co and Ce are often used.
- transition metal salts which are selected from the group of manganese and / or cobalt salts and / or complexes, more preferably from the group of the cobalt (amine) complexes, the cobalt (acetate) complexes, the Cobalt (carbonyl) complexes, the Chlori ⁇ de of cobalt or manganese and manganese sulfate.
- Zinc compounds or bismuth compounds can also be used to prevent corrosion on the items to be washed.
- Paraffin oils and silicone oils can optionally be used as defoamers and for the protection of plastic and metal surfaces.
- Defoamers are generally used in proportions of 0.001 wt .-% to 5 wt .-%.
- dyes such as, for example, patent blue, preservatives such as, for example, Kathon CG, pigments and other fragrances, may be added to the cleaning formulation according to the invention.
- a suitable filler is, for example, sodium sulfate.
- Rinses 2 rinses 55 ° C Normal (without pre-rinse)
- Washware Knife (WMF table knife Berlin, Monoblock) and keg glass cup (Matador, Ruhr Crystal), plastic plate: SAN plate Kayser ballast tableware: 6 dessert plate black
- Dishwashing detergent 6.5 g
- the evaluation of the dishes was carried out 18 hours after cleaning by visual Abmuste ⁇ tion in a black painted light box with halogen spot and pinhole using a grading scale from 10 (very good) to 1 (very bad).
- the highest grade of 10 corresponds to covering and drip-free surfaces, from grades ⁇ 5, coverings and drops are already visible under normal room lighting, so are perceived as disturbing.
- Polymer 1 copolymer of maleic acid and diisobutene (weight ratio 51: 49) with a molecular weight of 12,000 g / mol.
- Polymer 2 Copolymer of maleic anhydride, isobutene and C18 olefin (weight ratio 65: 26: 9), molecular weight 3,000 g / mol.
- Polymer 3 copolymer of maleic anhydride, C22- ⁇ -olefin, (weight ratio
- Polymer 4 copolymer of maleic acid and isobutene (weight ratio 68:32) having a molecular weight of 4,000 g / mol.
- Polymer 5 polyacrylic acid, molecular weight 8000 g / mol.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL05782771T PL1791936T3 (pl) | 2004-09-14 | 2005-09-13 | Preparaty czyszczące do maszynowego mycia naczyń zawierające hydrofobowo modyfikowane polikarboksylany |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102004044411A DE102004044411A1 (de) | 2004-09-14 | 2004-09-14 | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophob modifizierte Polycarboxylate |
PCT/EP2005/009819 WO2006029806A1 (de) | 2004-09-14 | 2005-09-13 | Reinigungsformulierungen für die maschinelle geschirrreinigung enthaltend hydrophob modifizierte polycarboxylate |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1791936A1 true EP1791936A1 (de) | 2007-06-06 |
EP1791936B1 EP1791936B1 (de) | 2012-02-22 |
Family
ID=35276092
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05782771A Not-in-force EP1791936B1 (de) | 2004-09-14 | 2005-09-13 | Reinigungsformulierungen für die maschinelle geschirrreinigung enthaltend hydrophob modifizierte polycarboxylate |
Country Status (10)
Country | Link |
---|---|
US (1) | US7557074B2 (de) |
EP (1) | EP1791936B1 (de) |
JP (1) | JP5065027B2 (de) |
CN (1) | CN101018849B (de) |
AT (1) | ATE546515T1 (de) |
CA (1) | CA2576300C (de) |
DE (1) | DE102004044411A1 (de) |
ES (1) | ES2378889T3 (de) |
PL (1) | PL1791936T3 (de) |
WO (1) | WO2006029806A1 (de) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004044411A1 (de) * | 2004-09-14 | 2006-03-30 | Basf Ag | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophob modifizierte Polycarboxylate |
DE102005041347A1 (de) * | 2005-08-31 | 2007-03-01 | Basf Ag | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophil modifizierte Polycarboxylate |
BRPI0715378A2 (pt) * | 2006-08-10 | 2013-06-18 | Basf Se | formulaÇço de limpeza para mÁquina de lavar louÇa, uso de uma combinaÇço de copolÍmeros e de agentes complexantes, e, processo para limpeza de louÇa em mÁquina |
DE102008000029A1 (de) | 2008-01-10 | 2009-07-16 | Lanxess Deutschland Gmbh | Geschirrreinigungsmittel |
DE102007003885A1 (de) | 2007-01-19 | 2008-07-24 | Lanxess Deutschland Gmbh | Geschirrreinigungsmittel |
DE102007044417A1 (de) * | 2007-09-17 | 2009-03-19 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007044418A1 (de) * | 2007-09-17 | 2009-03-19 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007006628A1 (de) * | 2007-02-06 | 2008-08-07 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007006627A1 (de) * | 2007-02-06 | 2008-08-07 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007006629A1 (de) | 2007-02-06 | 2008-08-07 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007006630A1 (de) * | 2007-02-06 | 2008-08-07 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
WO2008095554A2 (de) * | 2007-02-06 | 2008-08-14 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007006908A1 (de) * | 2007-02-13 | 2008-08-14 | Cht R. Beitlich Gmbh | Katalysierte Peroxidbleiche ("Katalysator-Bleiche") |
ES2576846T5 (es) | 2007-05-04 | 2022-02-23 | Ecolab Inc | Composiciones de limpieza sólidas |
DE102007042860A1 (de) * | 2007-09-10 | 2009-03-12 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
DE102007042907A1 (de) * | 2007-09-10 | 2009-03-12 | Henkel Ag & Co. Kgaa | Reinigungsmittel |
ATE522595T1 (de) * | 2007-10-12 | 2011-09-15 | Basf Se | Geschirrreinigungsformulierungen enthaltend ein gemisch aus hydrophob modifizierten polycarboxylaten und hydrophil modifizierten polycarboxylaten |
MX2010003825A (es) | 2007-10-18 | 2010-04-27 | Ecolab Inc | Composiciones de limpieza solidas, auto-solidificables, comprimidas, y metodos para hacerlas. |
DE102008063801A1 (de) | 2008-12-19 | 2010-06-24 | Henkel Ag & Co. Kgaa | Maschinelles Geschirrspülmittel |
DE102009017724A1 (de) * | 2009-04-11 | 2010-10-14 | Clariant International Limited | Bleichmittelgranulate |
DE102009029636A1 (de) | 2009-09-21 | 2011-03-24 | Henkel Ag & Co. Kgaa | Maschine Geschirrspülmittel |
JP5464755B2 (ja) * | 2010-03-09 | 2014-04-09 | ローム アンド ハース カンパニー | 自動食器洗いシステムのためのスケール低減添加剤 |
JP5377536B2 (ja) * | 2010-03-09 | 2013-12-25 | ローム アンド ハース カンパニー | 自動食器洗いシステムのためのスケール低減添加剤 |
EP2388308A1 (de) | 2010-05-19 | 2011-11-23 | Dequest AG | Reinigungsmittel mit verbesserter Fleckenentfernung |
EP2571971B1 (de) | 2010-05-19 | 2015-07-08 | Italmatch Chemicals S.P.A. | Reinigungsmittel mit verbesserter fleckenentfernung |
BR112015001051A2 (pt) * | 2012-07-27 | 2017-06-27 | Kao Corp | composição detergente sólida |
CN104508106B (zh) * | 2012-07-27 | 2017-08-08 | 花王株式会社 | 餐具用清洁剂组合物 |
JP5941812B2 (ja) * | 2012-09-28 | 2016-06-29 | 花王株式会社 | 食器用洗浄剤組成物 |
JP6027877B2 (ja) * | 2012-12-12 | 2016-11-16 | 花王株式会社 | 自動食器洗浄機用洗浄剤組成物 |
PL2997121T3 (pl) * | 2013-05-17 | 2019-05-31 | Unilever Nv | Kompozycja detergentowa do automatycznego mycia naczyń |
RU2016103485A (ru) * | 2013-07-04 | 2017-08-07 | Басф Се | Способ очистки посуды |
MX2016010709A (es) * | 2014-02-20 | 2016-11-10 | Unilever Nv | Composicion para el lavado de la vajilla a maquina. |
US9920288B2 (en) | 2014-07-11 | 2018-03-20 | Diversey, Inc. | Tablet dishwashing detergent and methods for making and using the same |
US9139799B1 (en) | 2014-07-11 | 2015-09-22 | Diversey, Inc. | Scale-inhibition compositions and methods of making and using the same |
WO2016175895A1 (en) | 2015-04-29 | 2016-11-03 | Shutterfly, Inc. | Image product creation based on face images grouped using image product statistics |
CN108137459B (zh) | 2015-10-07 | 2021-06-18 | 海名斯精细化工公司 | 润湿-防泡剂 |
WO2017189703A1 (en) | 2016-04-27 | 2017-11-02 | Dow Corning Corporation | Detergent composition comprising a carbinol functional trisiloxane |
CN107523428A (zh) * | 2017-07-28 | 2017-12-29 | 广州立白企业集团有限公司 | 洗涤剂组合物及其应用 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2064720C3 (de) * | 1970-12-31 | 1974-06-20 | Kube Kg, Kunkel & Co, 8999 Weiler | Anordnung zur temperaturabhängigen Steuerung der Ein- und Ausschaltdauer von Klimaanlagen, insbes. zur Verwendung bei Stallbelüftungen |
PH25826A (en) | 1986-03-14 | 1991-11-05 | Johnson & Son Inc S C | Prespotter laundry detergent |
US5232622A (en) * | 1990-06-20 | 1993-08-03 | Rohm And Haas Company | Chlorine-free machine dishwashing |
US5399285A (en) * | 1992-10-30 | 1995-03-21 | Diversey Corporation | Non-chlorinated low alkalinity high retention cleaners |
US6165970A (en) * | 1996-03-29 | 2000-12-26 | The Procter & Gamble Company | Detergent composition comprising acrylic acid-based polymer and amino tricarboxylic acid-based compound |
GB2311538A (en) | 1996-03-29 | 1997-10-01 | Procter & Gamble | Detergent compositions |
US6521576B1 (en) * | 2000-09-08 | 2003-02-18 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Polycarboxylic acid containing three-in-one dishwashing composition |
DE10104470A1 (de) * | 2001-02-01 | 2002-08-08 | Basf Ag | Reinigerformulierungen zur Verhinderung der Verfärbung von Kunststoffgegenständen |
DE10104469A1 (de) * | 2001-02-01 | 2002-08-08 | Basf Ag | Copolymere zur Verhinderung von Glaskorrosion |
PL202632B1 (pl) * | 2001-08-17 | 2009-07-31 | Henkel Ag & Co Kgaa | Środek do maszynowego natryskowego zmywania naczyń |
DE102004044411A1 (de) * | 2004-09-14 | 2006-03-30 | Basf Ag | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophob modifizierte Polycarboxylate |
-
2004
- 2004-09-14 DE DE102004044411A patent/DE102004044411A1/de not_active Withdrawn
-
2005
- 2005-09-13 WO PCT/EP2005/009819 patent/WO2006029806A1/de active Application Filing
- 2005-09-13 EP EP05782771A patent/EP1791936B1/de not_active Not-in-force
- 2005-09-13 US US11/574,890 patent/US7557074B2/en not_active Expired - Fee Related
- 2005-09-13 ES ES05782771T patent/ES2378889T3/es active Active
- 2005-09-13 JP JP2007531657A patent/JP5065027B2/ja not_active Expired - Fee Related
- 2005-09-13 PL PL05782771T patent/PL1791936T3/pl unknown
- 2005-09-13 AT AT05782771T patent/ATE546515T1/de active
- 2005-09-13 CA CA2576300A patent/CA2576300C/en not_active Expired - Fee Related
- 2005-09-13 CN CN2005800308488A patent/CN101018849B/zh not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
See references of WO2006029806A1 * |
Also Published As
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JP2008513557A (ja) | 2008-05-01 |
US7557074B2 (en) | 2009-07-07 |
PL1791936T3 (pl) | 2012-07-31 |
CN101018849A (zh) | 2007-08-15 |
CA2576300C (en) | 2013-12-24 |
US20070219110A1 (en) | 2007-09-20 |
CN101018849B (zh) | 2011-11-09 |
ES2378889T3 (es) | 2012-04-18 |
DE102004044411A1 (de) | 2006-03-30 |
WO2006029806A1 (de) | 2006-03-23 |
JP5065027B2 (ja) | 2012-10-31 |
ATE546515T1 (de) | 2012-03-15 |
CA2576300A1 (en) | 2006-03-23 |
EP1791936B1 (de) | 2012-02-22 |
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