EP4256016A1 - Reinigungszusammensetzung für harte oberflächen - Google Patents

Reinigungszusammensetzung für harte oberflächen

Info

Publication number
EP4256016A1
EP4256016A1 EP21810368.7A EP21810368A EP4256016A1 EP 4256016 A1 EP4256016 A1 EP 4256016A1 EP 21810368 A EP21810368 A EP 21810368A EP 4256016 A1 EP4256016 A1 EP 4256016A1
Authority
EP
European Patent Office
Prior art keywords
surfactant
composition according
betaine
alkyl
amine oxide
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.)
Pending
Application number
EP21810368.7A
Other languages
English (en)
French (fr)
Inventor
Arijit BERA
Jiji Paul Kottukapally
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unilever Global IP Ltd
Unilever IP Holdings BV
Original Assignee
Unilever Global IP Ltd
Unilever IP Holdings BV
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Unilever Global IP Ltd, Unilever IP Holdings BV filed Critical Unilever Global IP Ltd
Publication of EP4256016A1 publication Critical patent/EP4256016A1/de
Pending legal-status Critical Current

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
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/046—Salts
    • 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
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/94—Mixtures with anionic, cationic or non-ionic 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
    • 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
    • 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
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/75—Amino oxides
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88—Ampholytes; Electroneutral compounds
    • C11D1/90—Betaines
    • 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 hard surface cleaning compositions, in particular liquid aqueous detergent compositions comprising a surfactant system with a high Renewable Carbon Index (RCI) with good emulsification and oily soil removal of hard surfaces, such as tableware.
  • RCI Renewable Carbon Index
  • Household cleaning activities involve the use of a detergent product and water to rinse off the detergent product and finish the cleaning process. These activities are typically performed daily, often more than once a day, such as dish washing. That is, hard surface cleaning, dishwashing and other household cleaning activities are time consuming activities and, ideally, can be optimized when using products with excellent detergency and soil removal capacity.
  • the Renewable Carbon Index is a way to quantify the ‘eco-friendly’ profile of ingredients and products.
  • a further refined version of such an index is the Biorenewable Carbon Index (BCI) wherein at least part of the carbon in an ingredient or product is derived from recently living plant or animal organisms.
  • the surfactant system in cleaning product contributes to the cleaning efficacy in such products.
  • the RCI and BCI of surfactants may widely vary with some having a high RCI or BCI, like alkyl polyglycosides (APG) and rhamnolipids, because of their very nature, and other surfactants that are simply not available from a renewable source. It may not always be possible to formulate surfactant systems solely with surfactants like APG and rhamnolipids because of supply, cost and/or formulation restraints, and sometimes such surfactant mixes do not match the desired cleaning profile. Some of the most widely used surfactants are not (cost effectively) available as ingredients with a high RCI or BCI, like for example alkylbenzene sulphonates (ABS).
  • ABS alkylbenzene sulphonates
  • cleaning compositions comprising a surfactant system comprising anionic surfactant and amphoteric surfactant in certain weight ratios provide good oily soil removal whilst the surfactant system has a high Renewable Carbon Index (RCI).
  • RCI Renewable Carbon Index
  • the invention relates to a liquid aqueous detergent composition
  • a liquid aqueous detergent composition comprising, a. 8 to 30 wt% of a surfactant system comprising, i. primary surfactant being anionic surfactant comprising a surfactant of the formula (Ri-(OR’) n -O-SO3')xM x+ , wherein:
  • Ri is saturated or unsaturated Cs-C alkyl chain
  • R’ is ethylene; n is from 1 to 18; x is equal to 1 or 2;
  • M x+ is a suitable cation which provides charge neutrality selected from sodium, calcium, potassium and magnesium; and optionally comprising alkyl sulphate; and ii. secondary surfactant being amphoteric surfactant comprising betaine and amine oxide in a weight ratio of betaine to amine oxide in the range from 1:1 to 7:1 ; b. 0.001 to 0.2 wt% of polyethylene oxide having a molecular weight higher than 200,000 g/mol; c.
  • RTI Renewable Carbon Index
  • the invention further relates to a method of cleaning a hard surface using the composition of the invention, as well as the use thereof.
  • the liquid aqueous detergent composition of the present invention comprises a surfactant system.
  • the surfactant system comprises at least primary and secondary surfactant wherein the weight ratio of primary surfactant to secondary surfactant is in the range from 2:1 to 8:1. Preferably the weight ratio is from 4:1 to 7:1 , more preferably 5:1 to 7:1.
  • the surfactant system is present in the composition in a concentration of 8 to 30 wt%. Preferably the weight ratio of the surfactant system is 8 to 25 wt%, more preferably 9 to 20 wt% and even more preferably 9 to 15 wt%.
  • the primary surfactant is an anionic surfactant comprising a surfactant of the formula (Formula I):
  • Ri is saturated or unsaturated Cs-C , preferably C12-C14 alkyl chain; preferably, R1 is a saturated Cs-C , more preferably a saturated C12-C14 alkyl chain;
  • R’ is ethylene; n is from 1 to 18, preferably from 1 to 15, more preferably from 1 to 10, still more preferably from 1 to 5; x is equal to 1 or 2;
  • M x+ is a suitable cation which provides charge neutrality, preferably sodium, calcium, potassium, or magnesium, more preferably a sodium cation.
  • the primary surfactant comprises sodium lauryl ether sulphate having 1 to 3 ethylene oxide units per molecule, more preferably, sodium lauryl ether sulphate having 1 to 2 ethylene oxide units per molecule.
  • the primary surfactant comprises at least 70 wt% calculated on total amount of primary surfactant, more preferably at least 80 wt%, even more preferably at least 90 wt% and still more preferably at least 95 wt% surfactant of Formula I. It may be preferred that the primary surfactant consists of surfactant of Formula I.
  • the primary surfactant may optionally comprise alkyl sulphates, i.e. primary alcohol sulphates.
  • alkyl sulphates include sodium lauryl sulphate, ammonium lauryl sulphate and diethanolamine (DEA) lauryl sulphate.
  • DEA diethanolamine
  • Suitable examples include alkyl sulphates from synthetic origin with trade names Safol 23, Dobanol 23A or 23S, Lial 123 S, Alfol 1412S, Empicol LC3, Empicol 075SR.
  • Further suitable examples, and preferred when alkyl sulphates are present in the primary surfactant include alkyl sulphates commercially available from natural sources with trade names Galaxy 689, Galaxy 780, Galaxy 789, Galaxy 799 SP.
  • the primary surfactant may comprise other anionic surfactants such as rhamnolipids, being anionic biosurfactants.
  • Primary surfactant may be present in a concentration of 5 to 89 wt%, preferably 10 to 85 wt%, more preferably 15 to 80 wt%, even more preferably 20 to 70 wt% and still even more preferably 25 to 60 wt%, by total weight of the surfactant system.
  • the secondary surfactant is amphoteric surfactant comprising betaine and amine oxide in a weight ratio of betaine to amine oxide in the range from 1:1 to 7:1.
  • the specific weight ratio allows for improved emulsification in the compositions of the present invention.
  • the weight ratio of betaine to amine oxide is in the range from 2:1 to 6:1 , more preferably from 3:1 to 5:1. So for example, a weight ratio of 6:1 means that there is 6 times more betaine present than amine oxide.
  • the secondary surfactant comprises at least 70 wt% calculated on total amount of secondary surfactant, more preferably at least 80 wt%, even more preferably at least 90 wt% and still more preferably at least 95 wt% betaine and amine oxide. It may be preferred that the secondary surfactant consists of betaine and amine oxide.
  • Secondary surfactant may be present in a concentration of 0.1 to 30 wt%, preferably 0.5 to 25 wt%, more preferably 1 to 20 wt%, even more preferably 2 to 15 wt% and still even more preferably 3 to 10 wt% by total weight of the surfactant system.
  • Betaine The amphoteric surfactant comprises betaine.
  • Suitable betaines include alkyl betaine, alkyl amido betaine, alkyl amidopropyl betaine, alkyl sulphobetaine and alkyl phosphobetaine, wherein the alkyl groups preferably have from 8 to 19 carbon atoms.
  • cocodimethyl sulphopropyl betaine cetyl betaine, laurylamidopropyl betaine, caprylate/caprate betaine, capryl/capramidopropyl betaine, cocam idopropyl hydroxysultaine, cocobutyramido hydroxysultaine, and preferably lauryl betaine, cocamidopropyl betaine and sodium cocamphopropionate.
  • the betaine is cocamidopropyl betaine (CAPB).
  • the amphoteric surfactant comprises an amine oxide surfactant.
  • Preferred amine oxides are alkyl dimethyl amine oxide and alkyl amido propyl dimethyl amine oxide, more preferably alkyl dimethyl amine oxide.
  • Especially preferred are lauryl dimethylamine oxide, coco dimethyl amine oxide and coco amido propyl dimethyl amine oxide.
  • the surfactant system of the present invention may comprise other types of surfactants in addition to the anionic surfactant of the primary surfactant and amphoteric surfactant of the secondary surfactant. More specifically the surfactant system may also comprise cationic and/or non-ionic surfactant.
  • Suitable non-ionic surfactants include the condensation products of a higher alcohol (e.g. an alkanol containing about 8 to 18 carbon atoms in a straight or branched chain configuration) condensed with about 5 to 30 moles of ethylene oxide, for example, lauryl or myristyl alcohol condensed with about 16 moles of ethylene oxide (EO), tridecanol condensed with about 6 moles of EO, myristyl alcohol condensed with about 10 moles of EO per mole of myristyl alcohol, the condensation product of EO with a cut of coconut fatty alcohol containing a mixture of fatty alcohols with alkyl chains varying from 10 to about 14 carbon atoms in length and wherein the condensate contains either about 6 moles of EO per mole of total alcohol or about 9 moles of EO per mole of alcohol and tallow alcohol ethoxylates containing 6 EO to 11 EO per mole of alcohol.
  • a higher alcohol e.g. an
  • Lauryl alcohol condensed with 5, 7 and 9 moles of ethylene oxide (Laureth 5, Laureth 7 and Laureth 9).
  • the non-ionic surfactant is selected from Laureth 5, Laureth 7 and Laureth 9, or mixtures thereof.
  • Condensates of 2 to 30 moles of ethylene oxide with sorbitan mono- and tri-C10-C20 alkanoic acid esters having a HLB of 8 to 15 also may be employed as the nonionic surfactant.
  • These surfactants are well known and are available from Imperial Chemical Industries under the Tween trade name. Suitable surfactants include polyoxyethylene (4) sorbitan monolaurate, polyoxyethylene (4) sorbitan monostearate, polyoxyethylene (20) sorbitan trioleate and polyoxyethylene (20) sorbitan tristearate.
  • alkyl polyglycosides are alkyl polyglycosides. These may be preferred as these have a high Renewable Carbon Index (RCI) and Biorenewable Carbon Index (BCI).
  • RCI Renewable Carbon Index
  • BCI Biorenewable Carbon Index
  • the non-ionic surfactant is in a concentration of 0.1 to 5 % by weight, preferably at least 0.3%, still more preferably at least 0.5% but preferably not more than 4%, more preferably not more than 3%, even more preferably not more than 2% by weight of the surfactant system.
  • BKC benzalkonium chloride
  • Renewable carbon is defined as carbon derived from recently living plant or animal organisms (as opposed to carbon derived from fossil carbon which is coal, oil or petroleum based), as well as carbon derived from CO2 capture.
  • Biorenewable carbon is defined as carbon derived from recently living plant or animal organisms and as such has no carbon derived from fossil carbon which is coal, oil or petroleum based.
  • RCI is defined as the value calculated by dividing the number of renewable carbons by the total number of carbons in the entire molecule
  • BCI is defined as the value calculated by dividing the number of biorenewable carbons by the total number of carbons in the entire molecule. For example, if 80% of the number of carbons present in a surfactant system is renewable carbon then the RCI is 0.8.
  • the liquid detergent composition of the present invention comprises a surfactant system having a RCI of at least 0.8.
  • the surfactant system has a RCI of 1.
  • the surfactant system preferably has a BCI of at least 0.8.
  • the surfactant system has a BCI of 1 .
  • ABS Alkylbenzene sulphonates
  • Alkylbenzene sulphonates and derivatives thereof include water-soluble alkali metal salts of organic sulphonates having alkyl radicals typically containing from about 8 to about 22 carbon atoms, preferably 8 to 18 carbon atoms, still more preferably 12 to 15 carbon atoms and may be saturated or unsaturated.
  • Examples include sodium salt of linear alkylbenzene sulphonate, alkyl toluene sulphonate, alkyl xylene sulphonate, alkyl phenol sulphonate, alkyl naphthalene-sulphonate, ammonium diamylnaphthalenesulphonate and sodium dinonylnaphthalene-sulphonate and mixtures with olefin sulphonates.
  • ABS is not readily available from renewable carbon or biorenewable carbon sources. Therefore, any amount of ABS in the surfactant system of compositions of the present invention will not contribute to the RCI or BCI of the surfactant system. It is therefore preferred that the amount of ABS in the surfactant system is kept at very low levels like for example from 0 to 5 wt% or 0 to 3 wt% calculated on total surfactant system.
  • the surfactant system is essentially free of ABS and derivatives thereof wherein essentially free is defined as from 0 to 1 wt% calculated on total surfactant system. Even more preferably the surfactant system is free of ABS.
  • the liquid detergent composition of the present invention comprises polyethylene oxide having a molecular weight higher than 200,000 g/mol.
  • the polyethylene oxide may be present as a single compound or a mixture of at least two polyethylene oxides having a molecular weight higher than 200,000 g/mol.
  • polyethylene oxide refers to polyethylene oxides (PEO) or high molecular weight polyethylene glycols (PEGs).
  • high molecular weight polyethylene glycol means a linear homopolymer derived from ethylene oxide and having a molecular weight of at least 200,000 g/mol.
  • the polyethylene oxide has a molecular weight of 300,000 g/mol to 4,000,000 g/mol, more preferably 500,000 g/mol to 3,000,000 g/mol, even more preferably 1 ,000,000 to 2,000,000 g/mol.
  • Suitable examples include, but are not limited to, polyethylene oxides commercially available with trade names WSR N-10, WSR N-80, WSR N-750, WSR 205, WSR 1105, WSR N-12K, WSR N-60K, WSR-301, WSR-303, WSR-308, all from The Dow Chemical Company; polyethylene oxide (PEO) from MSE, Beantown chemicals or Acros Organics; PEO 100K from Polysciences; PEO-1 , PEO2, PEO-3, PEO-4, PEO-8, PEO15, PEO-18, PEO-57, PEO-29 from Sumitomo Seika Chemicals Ltd.; or ALKOX polyethylene Glycol from Meisei Chemical Works.
  • PEO polyethylene oxide
  • the polyethylene oxide is present in an amount of 0.001 to 0.2 wt.% based on the total weight of the composition.
  • the polyethylene oxide is present in an amount of 0.01 to 0.18, more preferably 0.1 to 0.15 wt.%.
  • the liquid detergent composition comprises 0.1 to 5% by weight of an inorganic salt selected from the group consisting of sodium chloride, magnesium sulfate, sodium sulfate and combinations thereof.
  • Inorganic salts advantageously control the viscosity of the detergent compositions.
  • liquid detergent composition comprises 0.5 to 4%, more preferably 1.0 to 3%, even more preferably 1.5 to 2.5 % by weight of an inorganic salt.
  • the composition further comprises water. Preferably 60 to 92%, more preferably not less than 62%, still more preferably not less than 65% but typically not more than 85%, more preferably not more than 80%, still more preferably not more than 75% by weight of the composition.
  • compositions according to the invention may contain other ingredients which aid in the cleaning or sensory performance.
  • Compositions according to the invention can also contain, in addition to the ingredients already mentioned, various other optional ingredients such as thickeners, colorants, preservatives, fatty acids, anti-microbial agents, perfumes, pH adjusters, sequestrants, alkalinity agents and hydrotropes.
  • compositions do not contain large amounts of organic solvents, usually added to boost cleaning performance, that is from 0 to 1 wt% organic solvent.
  • the composition is free of organic solvents.
  • compositions of the present invention preferably comprise only limited amounts of silicones as these may not provide the required user characteristics for cleaning compositions of the present invention. Silicones may for example leave a ‘slippery’ feel to the hard surface. Therefore, the composition of the present invention preferably comprises from 0 to 1 wt%, more preferably from 0 to 0.5 wt% and still more preferably from 0 to 0.1 wt% silicones. Still more preferably the composition is free of silicones. pH of the composition
  • the pH of the composition of the present invention is between 4.0 to 8.0.
  • the pH is 4.5 and 7.5, preferably between 4.5 and 7.0, more preferably between 5.0 and 6.5.
  • the composition of the present invention has a viscosity in the range of 1000 to 2700 cps at 21 sec 1 measured on a Haake Viscometer (Models include VT181 , VT501 , VT550 or equivalent) with “cup” and “bob” geometry, equipped with a MV cup and a MV2 bob at a controlled temperature of 25°C.
  • a Haake Viscometer Models include VT181 , VT501 , VT550 or equivalent
  • cup and “bob” geometry, equipped with a MV cup and a MV2 bob at a controlled temperature of 25°C.
  • 1500 to 2500 and more preferably 1700 to 2300 Thicker compositions are sometimes preferred by users as these may be easier to dose.
  • a thick product may also validate appropriate cleaning power perception with users of such compositions.
  • organic solvents like for example ethers, glycol ethers, ketones, diols, alcohols and combinations thereof are included to liquid aqueous detergent compositions to improve cleaning performance of such compositions.
  • organic solvents include low carbon alcohols like ethanol and isopropyl alcohol, alkoxylated aliphatic alcohols like butoxypropanol, and glycol ethers like ethylene glycol n-butyl ether, ethylene glycol propyl ether and dipropylene glycol dimethyl ether.
  • the liquid aqueous detergent compositions of the present invention preferably comprise 0 to 1 wt% of such organic solvents and more preferably 0 to 0.5 wt%. Even more preferably the liquid aqueous detergent composition is essentially free of organic solvents.
  • the composition may be used neat or diluted.
  • the composition is typically applied neat directly to the surface or on an implement like for example a sponge or cloth.
  • the composition is preferably diluted with water in a ratio of between 1 :1 to 1 :100 and more preferably in a ratio of between 1 :1 to 1:10.
  • composition may be packaged in the form of any commercially available bottle for storing the liquid.
  • the bottle containing the liquid can be of different sizes and shapes to accommodate different volumes of the liquid; preferably between 0.25 and 2 L, more preferably between 0.25 and 1.5 L or even between 0.25 and 1 L.
  • the bottle is preferably provided with a dispenser, which enables the consumer an easier mode of dispersion of the liquid. Spray or pump-dispensers may also be used.
  • the invention also relates to a method of cleaning a hard surface comprising the steps of: a. contacting the hard surface, optionally in diluted form, with the liquid detergent composition according to the present invention, and b. removing the detergent composition from the hard surface, optionally by rinsing with water.
  • the method can be performed manually (e.g. cleaning by hand) or in a cleaning device, such as an industrial or at home dishwashing machines.
  • a cleaning device such as an industrial or at home dishwashing machines.
  • the method of cleaning is a manual cleaning, more preferably hand dishwashing.
  • Hard surface typically means utensils or kitchenware, kitchen worktops, kitchen floors, sinks and kitchen counter tops, floors and bathrooms.
  • the invention relates to the use of a liquid detergent composition of the invention for handwashing hard surfaces, preferably dishware.
  • the composition of the invention is applied onto a hard surface in neat or diluted form.
  • the composition may be applied by any known ways such as by using a cleaning implement, such as scrub, sponge paper, cloth, wipes or any other direct or indirect application.
  • the applied composition may be cleaned using a cleaning implement such as a scrub, sponge, paper, cloth or wipes with or without water, or rinsed off with water, optionally running water.
  • Detergent compositions A (not according to the invention) and 1 to 4 (according to the invention) were prepared.
  • the pH of the formulations was around pH 6.
  • the formulations are included in Table 1. TABLE 1 , detergent compositions (wt%)
  • the formulations as in Table 1 were evaluated as to their emulsification capacity. 5 g of the formulation was poured into a 250 ml beaker, to which 50 ml of 24 FH. (‘French Hardness’) water at 25°C were added followed by stirring until dissolution. To the homogeneous mixture, 25 g of an oil mix consisting of 95 wt% sunflower oil, 2.5 wt% stearic acid and 2.5 wt% oleic acid was added. The mixture was stirred for 2 min at 1200 RPM and then transferred to a 250 ml glass cylinder.
  • the non-emulsified phase was measured (in mm) after 30 min from start time (1 st reading) and after 90 min from start time (2 nd reading).

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
EP21810368.7A 2020-12-07 2021-11-18 Reinigungszusammensetzung für harte oberflächen Pending EP4256016A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP20212124 2020-12-07
PCT/EP2021/082081 WO2022122332A1 (en) 2020-12-07 2021-11-18 A hard surface cleaning composition

Publications (1)

Publication Number Publication Date
EP4256016A1 true EP4256016A1 (de) 2023-10-11

Family

ID=73740237

Family Applications (1)

Application Number Title Priority Date Filing Date
EP21810368.7A Pending EP4256016A1 (de) 2020-12-07 2021-11-18 Reinigungszusammensetzung für harte oberflächen

Country Status (6)

Country Link
EP (1) EP4256016A1 (de)
CN (1) CN116529347A (de)
AR (1) AR125175A1 (de)
CL (1) CL2023001613A1 (de)
WO (1) WO2022122332A1 (de)
ZA (1) ZA202305088B (de)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1167500A1 (de) * 2000-06-29 2002-01-02 The Procter & Gamble Company Verfahren zum Reinigen einer harten Oberfläche
PL2420558T3 (pl) * 2010-08-17 2017-12-29 The Procter And Gamble Company Stabilne, trwałe detergenty do ręcznego zmywania naczyń
EP3670639A1 (de) * 2018-12-17 2020-06-24 Unilever N.V. Flüssige handgeschirrspülformulierung mit hydroxyfettsäure und polymer
WO2020126592A1 (en) * 2018-12-17 2020-06-25 Unilever N.V. Liquid hand dishwash formulation comprising fatty acids and polymer

Also Published As

Publication number Publication date
CN116529347A (zh) 2023-08-01
WO2022122332A1 (en) 2022-06-16
CL2023001613A1 (es) 2023-12-15
ZA202305088B (en) 2024-09-25
AR125175A1 (es) 2023-06-21

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