EP4479507B1 - Vormischung einer konzentrierten flüssigen zusammensetzung - Google Patents
Vormischung einer konzentrierten flüssigen zusammensetzungInfo
- Publication number
- EP4479507B1 EP4479507B1 EP23702839.4A EP23702839A EP4479507B1 EP 4479507 B1 EP4479507 B1 EP 4479507B1 EP 23702839 A EP23702839 A EP 23702839A EP 4479507 B1 EP4479507 B1 EP 4479507B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- composition
- composition premix
- premix
- water
- alkyl
- 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.)
- Active
Links
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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2093—Esters; Carbonates
-
- 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
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D11/00—Special methods for preparing compositions containing mixtures of detergents
- C11D11/0094—Process for making liquid detergent compositions, e.g. slurries, pastes or gels
-
- 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
-
- 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
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C11D17/042—Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
- C11D17/043—Liquid or thixotropic (gel) 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3707—Polyethers, e.g. polyalkyleneoxides
Definitions
- the present invention is in the field of cleaning compositions. More particularly, the present invention relates to a concentrated liquid composition premix for providing a liquid detergent on dilution in water.
- Laundry detergent, dishwash detergents, hard surface cleaners are examples of such cleaning compositions.
- Often detergents are available in various formats, such as, powder, bar, liquid, pods etc. Liquid format is one of the formats preferred by consumers.
- a liquid detergent may contain detersive actives, sequestrants, bleaching agents, soil release polymers, enzyme, antifoaming agent etc.
- such detergent contains significant amount of water.
- water acts as carrier for said ingredients and helps in forming a homogenous composition.
- high water content makes the product bulky.
- packaging of the product requires substantial amount of materials, such as, polyethylene, polyethylene terephthalate etc., which are often sourced from non-renewable resources. In this regard there is continuous effort to reduce such consumptions.
- One of the ways to reduce such consumptions is to have a product in liquid concentrated premix or dilutable format.
- a consumer is expected to dilute such product in water to form a liquid detergent and store it in a container.
- Such products are often termed as 'dilutable' or 'dilute at home' or 'Do it Yourself' (abbreviated as 'DiY'), which implies that consumers prepare their own detergent from a concentrated premix by adding water into in. This differs from in-use dilution, where the consumer doses an aliquot of the detergent into to a bucket of water or in tub of a washing machine forming a 'wash liquor' and use it for washing.
- 'Wash liquor' is typically low in detersive active content, has viscosity comparable to water and used immediately after preparation.
- 'dilutable' or 'dilute at home' or 'DiY' liquid detergents preferably contain higher amount of detersive actives and has certain product attributes. Viscosity is one of such attributes, which can be correlated to factors, such as, pourability of the product, ease of dissolution of the product when added in water and sensory of the product.
- liquid products in detergent context have certain viscosity significantly higher than water.
- liquid detergent formed on dilution of a 'dilutable' or 'dilute at home' or 'DiY' product or concentrated premix provides a cleaning benefit comparable with conventional liquid detergents available in the market.
- conventional liquid detergents may contain ingredients such as soil release polymer, antifoaming agent, enzyme and preservatives for enhanced cleaning benefits. Often such ingredients are solubilized or disperse homogenously in presence of water providing a stable product.
- a 'dilutable' or 'dilute at home' or 'DiY' or concentrated premix contain significantly low amount or no water. Thus, it is challenging to formulate a stable liquid concentrated premix product with such ingredients.
- liquid detergent formed on dilution of a 'DiY' or 'dilute at home' product or concentrated premix has viscosity such that a consumer can relate it with conventional liquid detergents available in market, i.e., viscosity of the liquid detergent should be comparable with conventional liquid detergent available in market,
- compositions comprising oxylakoylated polyglycerol esters, one or more organic solvents and water.
- EP 3 714 945 A1 discloses a liquid thickener composition comprising polyalkoxylated polyol polyester having guerbet moieties. Compounds contained therein relate to polyalkoxylated polyol polyester having a viscosity allows a product to be poured.
- the present inventors surprisingly found that an alkoxylated polyol polyester based associative polymer and an anionic surfactant with ammoniacal counterion provides a stable and isotropic composition premix.
- the composition premix provides a liquid detergent on dilution in water, which has a viscosity comparable or higher than the composition premix and it is similar to conventional liquid detergents.
- the present invention provides a concentrated liquid composition premix for forming a liquid detergent on dilution in water comprising:
- the present invention provides a unit dose product for providing a liquid detergent on dissolution in water comprising a composition premix according to the first aspect contained in a water-dissoluble pouch.
- liquid detergent obtained by dissolving a composition premix according to the first aspect in water, wherein the ratio of the composition premix to water is in the range 1:1 to 1:20 by weight.
- the present invention provides a process for providing a liquid detergent comprising steps of diluting a composition premix according to the first aspect in water, wherein the ratio of the composition premix to water is in the range from 1:1 to 1: 20 by weight.
- concentrated liquid composition premix comprising:
- composition premix comprises an anionic surfactant with an ammoniacal counterion.
- the anionic surfactant with an ammoniacal counterion is selected from alkyl ether sulphates, linear alkyl benzene sulphonates and combinations thereof with an ammoniacal counterion.
- ammoniacal counterions is selected from monoisopropylamine (MIPA), monoisopropylamine, ammonium, monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA) and triisopropanolamine (TIPA).
- MIPA monoisopropylamine
- MEA monoethanolamine
- DEA diethanolamine
- TIPA triethanolamine
- combinations of such counterions are also within the scope of the present invention.
- the anionic surfactant comprises a linear alkylbenzene sulphonate with monoethanolamine (MEA-LAS) and/or linear alkylbenzene sulphonate with monoisopropanolamine (MIPA-LAS).
- MEA-LAS monoethanolamine
- MIPA-LAS monoisopropanolamine
- the anionic surfactant comprises alkyl ether sulphate (AES) with an ammoniacal counterion.
- AES alkyl ether sulphate
- the alkyl ether sulphate (AES) has alkyl chain containing from about 8 to 22 carbon atoms.
- alkyl being used to include the alkyl portion of higher acyl radicals.
- the alkyl radicals preferably contain from 10 to 18, more preferably 12 to 14 carbon atoms and may be unsaturated.
- the alkyl ether sulphate may contain from 1 to 10 ethylene oxide (EO) or propylene oxide units per molecule, preferably contain 1 to 7, more preferably 1 to 5 and most preferably 1 to 3 ethylene oxide (EO) units per molecule.
- the anionic surfactant comprises alkyl ether sulphates having a straight or branched chain alkyl group having 12 to 14 carbon atoms and containing an average of 1 to 3 ethylene oxide (EO) units per molecule.
- EO ethylene oxide
- a preferred example is lauryl ether sulphate (SLES) with an ammoniacal counterion, in which the predominantly C12 lauryl alkyl group has been ethoxylated with an average of 3 ethylene oxide (EO) units per molecule.
- the anionic surfactant comprises alkyl ether sulphate (LES) with monoisopropanolamine (MIPA).
- LES alkyl ether sulphate
- MIPA monoisopropanolamine
- the anionic surfactant includes alkyl sulphate surfactant (PAS), such as non-ethoxylated primary and secondary alkyl sulphates having alkyl chain length with 10 to 18 carbon atoms.
- PAS alkyl sulphate surfactant
- the amount of the anionic surfactant is in the range 30 to 90 %wt. of the composition premix.
- the amount of the anionic surfactant is in the range 35 to 85 %wt., more preferably 40 to 80 %wt. and most preferably 45 to 75% wt. of the composition premix.
- a higher alcohol e.g., an alkanol
- Examples of the secondary alcohol ethoxylate suitable for the invention include those with an alkyl chain with a secondary ethoxylate joined thereto.
- the secondary ethoxylate comprises from 2 to 20 EO groups, preferably from 5 to 12 and most preferably 9 EO groups.
- the alkyl chain preferably comprises from 8 to 22 carbons, more preferably from 10 to 14 and most preferably 12.
- the alkyl chain is preferably saturated.
- Secondary ethoxylates suitable for the invention available commercially under tradename Tergitol ® from Dow.
- the composition premix comprises an alkoxylated polyol polyester.
- the alkoxylated polyol polyester comprises at least three alkoxylates and at least two C8 to C40 fatty acid ester.
- each alkoxylate group comprises 30 to 150, even more preferably 30 to 120 and most preferably 30 to 80 alkoxylate units on average per polyol.
- Examples include, but not limited to, mannitol, sorbitol, galactitol, fucitol, iditol, inositol, volemitol, isomalt, maltitol, lactitol, maltotritol, maltotetraitol, and polyglycitol;
- Disaccharide which is formed from two monosaccharide by dehydration via glycosidic linkage, examples include but not limited to, trehalose, sucrose, lactose, and maltose; Dextrin with a chemical structure of (C6H10O5)n, where n is from 2 to 20; Pentaerythritol and di-pentaerythritol; Dendrimer polyols, for examples, Bolton(R)H2004, H2003, and H20 have 6, 12, and 16 terminal hydroxyls, respectively; Polyglyceryls with 3 to 10 glycerin units, with
- the polyol is selected from polyols having 3 to 6 hydroxyl groups, more preferably selected from sorbitol, pentaerythritol and glycerol.
- the alkoxylated polyol polyester comprises at least two C4 to C40 fatty acid ester.
- the fatty acid ester has 10 to 30, more preferably 12 to 24 and most preferably 14 to 22 carbon atoms.
- the fatty acid ester independently selected from laurate, stearate, iso-stearate, guerbet acid ester and combinations thereof.
- the alkoxylated polyol polyester is available with an organic career selected from of mono or polyhydric alcohols and ether, ester or amide derivatives and hydrophobic thickeners containing non-ionic alkanolamines, ethoxylated C10 to C14 alcohols, liquid alkanolamines and combinations thereof.
- Preferred alkoxylated polyol polyesters include 40-50% PEG/PPG-120/10 trimethylolpropane trioleate; lauryl polyoxyl-6 glycerides / hydrogenated palm/palm kernel oil PEG-6 esters; PEG-150 pentaerythrityl tetra-stearate, PEG-150 pentaerythrityl tetra-stearate; PEG-20 glyceryl tristearate, PEG-20 glyceryl tri-isostearate, PEG-10 glyceryl trioleate, PEG-40 glyceryl trioleate, PEG-60 glyceryl trioleate; sorbeth-230 tetraoleate; and PEG-120 methyl glucose trioleate, PEG-120 methyl glucose trioleate.
- the composition premix preferably comprises a sequestrant.
- the sequestrant is selected from organic detergent builders or sequestrant materials. Examples include the alkali metal, citrates, succinates, malonates, carboxymethyl succinates, carboxylates, polycarboxylates and polyacetyl carboxylates. Specific examples include sodium, potassium and lithium salts of oxydisuccinic acid, mellitic acid, benzene polycarboxylic acids, and citric acid. Other examples are DEQUEST TM , organic phosphonate type sequestering agents sold by Monsanto and alkanehydroxy phosphonates.
- suitable organic builders/sequestrants include the higher molecular weight polymers and copolymers known to have builder properties.
- such materials include appropriate polyacrylic acid, polymaleic acid, and polyacrylic/polymaleic acid copolymers and their salts, for example those sold by BASF under the name SOKALAN TM .
- composition premix may comprise 0.5 to 20% wt. more preferably 1 to 10% wt. of sequestrant.
- sequestrant is Dequest ® 2066 (Diethylenetriamine penta(methylene phosphonic acid) or Heptasodium DTPMP).
- Other suitable sequestrant is 1 -Hydroxyethylidene -1,1, -diphosphonic (HEDP) acid and methylglycinediacetic acid (MGDA).
- the composition premix is in liquid concentrate format.
- the composition premix comprises less than 10% wt. water.
- the amount of water includes the amount added to the composition premix during preparation and the amount added along with a further raw material in which it is incorporated.
- surfactants are commercially available as aqueous solutions or suspensions of surfactants.
- the composition premix comprises less than 5% wt. water, and most preferably less than 1% wt. water.
- the composition is visually clear.
- visually clear' herein refer to a turbidity of less than 30 NTU (Nephelometric Turbidity Unit) at 25° C.
- the non-aqueous solvent comprises a hydrotrope.
- Hydrotrope are typically low molecular weight, water-soluble or water-miscible organic liquids such as C1 to C5 monohydric alcohols (such as ethanol and n- or i-propanol); C2 to C6 diols, e.g., monopropylene glycol and dipropylene glycol; C3 to C9 triols, e.g., glycerol; polyethylene glycols having a weight average molecular weight (Mw) ranging from about 200 to 600, and alkyl aryl sulfonates having up to 3 carbon atoms in the lower alkyl group, e.g., sodium and potassium salt of xylene, toluene, ethylbenzene and isopropyl benzene (cumene) sulfonates. Mixtures of any of said materials may also be used.
- Most preferred non-aqueous solvent is monopropy
- non-aqueous solvent suitable for the invention examples include glycol ethers such as diethylene glycol alkyl ether, dipropylene glycol alkyl ether, dipropylene dimethyl ether etc.; alkyl esters such as, alkyl levulinate, alkyl octanoate, methyl and alkyl soyate, etc.; C1 to C4 alkyl amide such as N, N-dimethyl alkenamide, more preferably N, N-dimethyl decenamide; alkyl alkoxylate such as benzyl alkoxylate.
- glycol ethers such as diethylene glycol alkyl ether, dipropylene glycol alkyl ether, dipropylene dimethyl ether etc.
- alkyl esters such as, alkyl levulinate, alkyl octanoate, methyl and alkyl soyate, etc.
- C1 to C4 alkyl amide such as N, N-dimethyl alkenamide, more
- composition premix may comprise 0.1 to 20% wt., more preferably 0.5 to 18% wt., even more preferably 1 to 16 %wt., and most preferably 3 to 15 %wt. of non-aqueous solvent.
- composition premix preferably comprises an effective amount of one or more enzyme preferably selected from the group comprising, hemicellulases, peroxidases, proteases, cellulases, hemicellulases, xylanases, xantanase, lipases, phospholipases, esterases, cutinases, pectinases, carrageenases, mannanases, pectate lyases, keratinases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, ⁇ -glucanases, arabinosidases, hyaluronidase, chondroitinase, laccase, tannases, amylases, nucleases (such as deoxyribonuclease and/or ribonuclease), phosphodiesterases,
- the level of an enzyme is from 0.1 to 600, more preferably from 0.5 to 450, most preferably from 1 to 400 mg active enzyme protein per 100 g finished product.
- the protease enzyme is present in the greatest weight fraction.
- the protease is present a level that are greater than 3 times any other single enzyme.
- Examples of preferred enzymes are sold under the following trade names Purafect Prime ® , Purafect ® , Preferenz ® (DuPont), Savinase ® , Pectawash ® , Mannaway ® , Lipex ® , Lipoclean ® , Whitzyme ® Stainzyme ® , Stainzyme Plus ® , Natalase ® , Mannaway ® , Amplify ® Xpect ® , Celluclean ® (Novozymes), Biotouch (AB Enzymes), Lavergy ® (BASF)
- Detergent enzymes are discussed in WO 2020/186028(Procter and Gamble ), WO 2020/200600 (Henkel ), WO 2020/070249 (Novozymes ), WO 2021/001244 (BASF ) and WO 2020/259949 (Unilever ).
- a nuclease enzyme is an enzyme capable of cleaving the phosphodiester bonds between the nucleotide sub-units of nucleic acids and is preferably a deoxyribonuclease or ribonuclease enzyme.
- composition premix may further comprise performance boosting polymers, such as soil release polymer (SRP) and/or anti-redeposition polymers (ARP).
- SRP soil release polymer
- ARP anti-redeposition polymers
- the water-soluble pouch made of water-soluble film.
- the water-soluble film comprises a water dissoluble material, such as polyvinyl alcohol (PVOH), including homopolymers thereof (e.g., including substantially only vinyl alcohol and vinyl acetate monomer units) and copolymers thereof (e.g., including one or more other monomer units in addition to vinyl alcohol and vinyl acetate units).
- PVOH polyvinyl alcohol
- the water-soluble film comprises partially hydrolysed PVOH.
- water soluble polymers for use in addition to the PVOH polymers and PVOH copolymers in the blend can include, but are not limited to modified polyvinyl alcohols, polyacrylates, water-soluble acrylate copolymers, polyvinyl pyrrolidone, polyethyleneimine, pullulan, water-soluble natural polymers including, but not limited to, guar gum, gum Acacia, xanthan gum, carrageenan, and starch, water-soluble polymer derivatives including, but not limited to, modified starches, ethoxylated starch, and hydroxypropylated starch, copolymers of the forgoing and combinations of any of the foregoing.
- water-soluble polymers can include polyalkylene oxides, polyacrylamides, polyacrylic acids and salts thereof, celluloses, cellulose ethers, cellulose esters, cellulose amides, polyvinyl acetates, polycarboxylic acids and salts thereof, polyaminoacids, polyamides, gelatines, methylcelluloses, carboxymethylcelluloses and salts thereof, dextrins, ethylcelluloses, hydroxyethyl celluloses, hydroxypropyl methylcelluloses, maltodextrins, and polymethacrylates.
- Such water-soluble polymers, whether PVOH or otherwise are commercially available from a variety of sources. Any of the foregoing water-soluble polymers are generally suitable for use as film-forming polymers.
- the water- soluble film can include copolymers and/or blends of the foregoing resins.
- the water-soluble film may further contain other auxiliary agents and processing agents, such as, but not limited to, plasticizers, plasticizer compatibilizers, surfactants, lubricants, release agents, fillers, extenders, cross-linking agents, antiblocking agents, antioxidants, detackifying agents, antifoams, nanoparticles such as layered silicate-type nanoclays (e.g., sodium montmorillonite), bleaching agents (e.g., sodium metabisulphite, sodium bisulphite or others), aversive agents such as bitterants (e.g., denatonium salts such as denatonium benzoate, denatonium saccharide, and denatonium chloride; sucrose octaacetate; quinine; flavonoids such as quercetin and naringen; and quassinoids such as quassin and brucine) and pungents (e.g., capsaicin, piperine, allyl isothiocyanate, and resinferat
- suitable polymers include polyesters, polyolefins, polyamides, polystyrene (PS), polyanhydrides, polyacrylates, poly hydroxy alkanoates, poly vinyl chloride, thermoplastic polyurethanes, polycarbonate (PC), polylactic acid (PLA), acrylonitrile/butadiene/styrene copolymer (ABS), styrene/acrylonitrile copolymer (SAN), polyoxymethylene (POM), biodegradable thermoplastics, starch-based thermoplastics, their derivatives, and combination thereof.
- a liquid detergent obtained by diluting the composition premix in water wherein the ratio of the composition premix to water is in the range from 1:1 to 1:20.
- the ratio of the composition premix to water is in the range from 1:2 to 1:15, even more preferably from 1:3 to 1:10 and yet more preferably 1:4 to 1:8 by weight.
- Most preferred dilution ratio of the composition premix to water is 1:5.
- a process for providing a liquid detergent for cleaning comprising steps of diluting a concentrated liquid composition premix according to the present invention in water, wherein the ratio of the composition premix to water is in the range from 1:1 to 1:20 by weight. More preferably the ratio of the composition premix to water is in the range from 1:2 to 1:15, even more preferably from 1:3 to 1:10 and yet more preferably 1:4 to 1:8 by weight. Most preferred dilution ratio of the composition premix to water is 1:5.
- the resulting liquid detergent is homogenous, stable and may be kept by the consumer until ready for use.
- the liquid detergent provided on dilution has viscosity in the range from 100 to 2000 mPa.S, more preferably 200 to 1600 mPa.S, and most preferably 300 to 1200 mPa.S at 20 S -1 shear rate and 25 °C.
- the liquid detergent has a viscosity comparable or higher than that of the composition premix.
- the liquid detergent may be a laundry or dishwashing detergent.
- Viscosity of each sample were measured using Rheocompass (Anton Paar GmbH), at 21S -1 shear rate and (25 ⁇ 2) °C with CP50 geometry and are summarized below: Table 2: Ex-1 Viscosity @ neat 380 Viscosity 1:5 dilution @21S -1 850
- Ex 1 shows viscosity build-up i.e., having higher viscosity on dilution.
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)
- Dispersion Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Claims (14)
- Konzentrierte flüssige Vormischungszusammensetzung zur Bildung eines flüssigen Reinigungsmittels bei Verdünnen in Wasser, umfassend:a) 30 bis 90 Gew.-% anionisches Tensid mit einem ammoniakalischen Gegenion; undb) einen alkoxylierten Polyolpolyester, der mindestens drei Alkoxylate und mindestens zwei C8- bis C40-Fettsäureester umfasst.
- Vormischungszusammensetzung nach Anspruch 1, wobei das anionische Tensid mit einem ammoniakalischen Gegenion unter Alkylethersulfaten, linearen Alkylbenzolsulfonaten und Kombinationen davon mit einem ammoniakalischen Gegenion ausgewählt ist.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 oder 2, wobei das ammoniakalische Gegenion unter Monoisopropanolamin (MIPA), Monoethanolamin (MEA), Diethanolamin (DEA) und Triethanolamin (TEA) ausgewählt ist.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 3, wobei die Menge des alkoxylierten Polyolpolyesters in dem Bereich von 0,1 bis 15 Gew.-% der Vormischungszusammensetzung liegt.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 4, wobei der alkoxylierte Polyolpolyester 50 bis 500 Alkoxylateinheiten umfasst.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 5, wobei das Alkoxylat Ethoxylat oder Propoxylat ist.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 6, wobei das Polyol unter Sorbit, Pentaerythrit und Glycerin ausgewählt ist.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 7, wobei der Fettsäureester unter Laurat, Stearat, Isostearat, Oleat, Guerbetsäureester und Kombinationen davon ausgewählt ist.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 8, die ein nichtionisches Tensid umfasst.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 9, wobei die Zusammensetzung 0,1 bis 15 Gew.-% nichtwässriges Lösungsmittel umfasst.
- Vormischungszusammensetzung nach Anspruch 10, wobei das nichtwässrige Lösungsmittel Monopropylenglykol umfasst.
- Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 11, wobei die Zusammensetzung weniger als 10 Gew.-% Wasser enthält.
- Einheitsdosisprodukt zur Bildung eines flüssigen Reinigungsmittels beim Auflösen in Wasser, umfassend eine Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 12, enthalten in einem wasserlöslichen Beutel.
- Verfahren zur Bereitstellung eines flüssigen Reinigungsmittels, umfassend die Schritte des Verdünnens einer Vormischungszusammensetzung nach irgendeinem der Ansprüche 1 bis 12 in Wasser, wobei das Gewichtsverhältnis der Vormischungszusammensetzung zu Wasser in dem Bereich von 1:1 bis 1:20 liegt.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP22156472 | 2022-02-14 | ||
| PCT/EP2023/052869 WO2023152092A1 (en) | 2022-02-14 | 2023-02-06 | A concentrated liquid composition premix |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP4479507A1 EP4479507A1 (de) | 2024-12-25 |
| EP4479507B1 true EP4479507B1 (de) | 2025-08-20 |
| EP4479507C0 EP4479507C0 (de) | 2025-08-20 |
Family
ID=80682528
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP23702839.4A Active EP4479507B1 (de) | 2022-02-14 | 2023-02-06 | Vormischung einer konzentrierten flüssigen zusammensetzung |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP4479507B1 (de) |
| AR (1) | AR128512A1 (de) |
| WO (1) | WO2023152092A1 (de) |
| ZA (1) | ZA202405312B (de) |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005506989A (ja) * | 2001-10-18 | 2005-03-10 | ザ プロクター アンド ギャンブル カンパニー | アニオン性界面活性剤、両性界面活性剤及びカチオン性ポリマーを有するシャンプー組成物 |
| DE10342870A1 (de) | 2003-09-15 | 2005-05-12 | Clariant Gmbh | Flüssige Zusammensetzungen enthaltend oxalkylierte Polyglycerinester |
| US9862913B2 (en) | 2010-12-13 | 2018-01-09 | Colgate-Palmolive Company | Dilutable concentrated cleaning composition |
| EP2922939A2 (de) * | 2012-11-21 | 2015-09-30 | Dow Corning Corporation | Stoffpflegezusammensetzungen mit emulsionen |
| BR102015028047A2 (pt) | 2015-11-06 | 2017-05-09 | Oxiteno S A Indústria E Comércio | composição espessante líquida para formulações de cosméticos para limpeza da pele e cabelos e limpadores de superfícies e tecidos, e, uso da composição espessante líquida |
| WO2020070249A1 (en) | 2018-10-03 | 2020-04-09 | Novozymes A/S | Cleaning compositions |
| CA3127167A1 (en) | 2019-03-14 | 2020-09-17 | The Procter & Gamble Company | Cleaning compositions comprising enzymes |
| EP3714945A1 (de) | 2019-03-29 | 2020-09-30 | Applechem Inc. | Flüssigkeitsverdickungsmittelzusammensetzung mit polyester mit polyalkoxylierten polyolen mit guerbet-säureteilen |
| DE102019204792A1 (de) | 2019-04-04 | 2020-10-08 | Henkel Ag & Co. Kgaa | Verwendung von Mannanase-Enzym in Kombination mit Catecholderivaten |
| US20220372408A1 (en) | 2019-06-28 | 2022-11-24 | Conopco, Inc., D/B/A Unilever | Detergent composition |
| EP3994148A1 (de) | 2019-07-01 | 2022-05-11 | Basf Se | Peptideacetale zur stabilisierung von enzymen |
| WO2021239376A1 (en) * | 2020-05-27 | 2021-12-02 | Unilever Ip Holdings B.V. | Dilutable fabric conditioner composition |
-
2023
- 2023-02-06 WO PCT/EP2023/052869 patent/WO2023152092A1/en not_active Ceased
- 2023-02-06 EP EP23702839.4A patent/EP4479507B1/de active Active
- 2023-02-14 AR ARP230100334A patent/AR128512A1/es unknown
-
2024
- 2024-07-08 ZA ZA2024/05312A patent/ZA202405312B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AR128512A1 (es) | 2024-05-15 |
| WO2023152092A1 (en) | 2023-08-17 |
| EP4479507C0 (de) | 2025-08-20 |
| ZA202405312B (en) | 2025-10-29 |
| EP4479507A1 (de) | 2024-12-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5535903B2 (ja) | ポリアルキレンオキシド及びビニルエステルをベースとする両親媒性グラフトポリマーを含む洗濯洗剤組成物 | |
| CN106471111B (zh) | 洗衣液组合物 | |
| EP1771535B1 (de) | Methylesterbasierte mikroemulsionen zum reinigen von festen oberflächen | |
| AU2013298898B2 (en) | Concentrated liquid detergent compositions | |
| EP3039111B1 (de) | Wässrige flüssige zusammensetzungen | |
| US7091168B2 (en) | Liquid detergents | |
| US20120122753A1 (en) | Liquid washing or cleaning agent comprising anti-graying polysaccharide | |
| US9012388B2 (en) | Gel surfactant composition | |
| WO2021222190A1 (en) | Liquid laundry composition | |
| WO2024017614A1 (en) | A concentrated liquid composition | |
| EP4479506B1 (de) | Vormischung einer konzentrierten flüssigen zusammensetzung | |
| EP4259762B1 (de) | Zusammensetzung | |
| WO2017174258A1 (en) | Laundry liquid composition | |
| EP4479507A1 (de) | Vormischung für konzentrierte flüssige zusammensetzung | |
| WO2024042179A1 (en) | A cleaning composition | |
| WO2024017623A1 (en) | A concentrated liquid composition | |
| EP2607469A1 (de) | Flüssiges Waschmittel mit Protease und Lipase | |
| EP4053254B1 (de) | Reinigungszusammensetzung mit polyalkylenglykol für harte oberflächen | |
| WO2026069388A1 (en) | Alkaline laundry liquid composition comprising sodium alkyl benzene sulphonate | |
| EP4547803A1 (de) | Stoff- und heimpflegeprodukt | |
| WO2021222191A1 (en) | Method of making liquid laundry detergent formulation | |
| JP2011026430A (ja) | 液体洗浄剤組成物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
| 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: REQUEST FOR EXAMINATION WAS MADE |
|
| 17P | Request for examination filed |
Effective date: 20240709 |
|
| 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 ME 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 |
|
| DAV | Request for validation of the european patent (deleted) | ||
| DAX | Request for extension of the european patent (deleted) | ||
| INTG | Intention to grant announced |
Effective date: 20250430 |
|
| GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
| 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 |
|
| 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 ME MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
| 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: IE Ref legal event code: FG4D |
|
| RAP4 | Party data changed (patent owner data changed or rights of a patent transferred) |
Owner name: UNILEVER IP HOLDINGS B.V. Owner name: UNILEVER GLOBAL IP LIMITED |
|
| U01 | Request for unitary effect filed |
Effective date: 20250820 |
|
| U07 | Unitary effect registered |
Designated state(s): AT BE BG DE DK EE FI FR IT LT LU LV MT NL PT RO SE SI Effective date: 20250826 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20251220 |
|
| 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: 20251120 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20250820 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20251121 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20250820 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20251120 |
|
| 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: 20250820 |
|
| U1N | Appointed representative for the unitary patent procedure changed after the registration of the unitary effect |
Representative=s name: UNILEVER PATENT GROUP; NL |
|
| U20 | Renewal fee for the european patent with unitary effect paid |
Year of fee payment: 4 Effective date: 20260225 |
|
| 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: 20250820 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20250820 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
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: 20250820 |