EP4242287A1 - Détergent pour lessive - Google Patents

Détergent pour lessive Download PDF

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Publication number
EP4242287A1
EP4242287A1 EP23156278.6A EP23156278A EP4242287A1 EP 4242287 A1 EP4242287 A1 EP 4242287A1 EP 23156278 A EP23156278 A EP 23156278A EP 4242287 A1 EP4242287 A1 EP 4242287A1
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EP
European Patent Office
Prior art keywords
acid
weight
range
laundry
detergent
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
EP23156278.6A
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German (de)
English (en)
Inventor
Nahla ELGHANDOUR
Sayed FARAHAT
Elron Gomes
Ahmed Amgad
Christina Roeleke
Detlef Buisker
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP4242287A1 publication Critical patent/EP4242287A1/fr
Pending legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3707Polyethers, e.g. polyalkyleneoxides
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06Powder; Flakes; Free-flowing mixtures; Sheets
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/046Salts
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads

Definitions

  • the present invention relates to surfactant-containing laundry detergents that comprise high molecular weight polyethylene oxide), fumed silica, and calcium salt. It also relates to the use of the combination of said ingredients to prevent accumulation of stains on fabrics by applying said combination in water to the fabrics, and to a process of laundering fabrics which makes use of said combination.
  • Laundry detergents generally contain, in addition to the ingredients such as surfactants and builder materials that are indispensable for the washing process, further constituents that can be grouped under the heading of "washing adjuvants" and encompass such different groups of active substances as foam regulators, greying inhibitors, bleaching agents, bleach activators, and color transfer inhibitors. Also included among such adjuvants are substances that impart soil-repelling properties to the laundry fibers and that, if present during the washing operation, assist the soil-releasing capability of the other laundry-detergent constituents.
  • Soil-release-enabling substances of this kind are often referred to as “soil release” active substances or, because of their ability to make the treated surface (for example, of the fibers) less prone to stains adhering to it, as “soil repellents.”
  • soil-release-enabling action of, for example methyl cellulose is known. Because of their chemical similarity to polyester fibers, soil-release-enabling active substances that are particularly effective for textiles made of said material are copolyesters that contain dicarboxylic acid units, alkylene glycol units, and polyalkylene glycol units. Soil-release-enabling copolyesters of the aforesaid kind, and the use thereof in laundry detergents, have been known for some time.
  • One aspect of the present invention is a solid laundry detergent in powder form, preferably suitable for washing fabrics by hand, comprising surfactant and a combination of polyethylene oxide) in which the medium polymerization degree of the ethylene oxide is in the range of from 22,000 to 228,000, fumed silica, and at least one calcium salt.
  • the mean molecular weight (weight average, M w ) of said polyethylene oxide) preferably is in the range of from 1,000,000 g/mol to 10,000,000 g/mol.
  • Preferred anions in the calcium salts are acetate, benzoate, borate, bromide, butyrate, carbonate, chloride, citrate, formate, fumarate, gluconate, iodide, lactate, malate, maleate, malonate, nitrate, oxalate, phosphate, propionate, salicylate, silicate, succinate, sulfate, tartrate, and mixtures thereof. More preferred are carbonate, sulfate, and their mixtures.
  • the weight ratio of said polyethylene oxide) to fumed silica is in the range of from 25 : 1 to 40 : 1, and/or that the weight ratio of said polyethylene oxide) to calcium salt is in the range of from 55 : 1 to 40 : 1.
  • Another aspect of the invention is the use of a combination defined above to prevent accumulation of stains on fabrics by applying said combination in water to the fabrics.
  • Still another aspect of the invention is the use, by treating fabrics with a combination defined above in water, to facilitate the removal of stains, accumulated on fabrics after the treatment, when washed. This washing of fabrics after the accumulation of stains may be performed with any common detergent, but preferably is performed with a detergent according to the invention in order to prolong the positive effects of the present invention.
  • detergents comprising the combination defined above do also show an improved detergency in comparison to detergents not comprising it. Accordingly, another aspect of the present invention is the use of the combination defined above to increase detergency of detergents.
  • Another aspect of the invention is a process of hand washing laundry, by manually contacting laundry in need of washing with an aqueous laundry liquor comprising 2.2 g/l to 2.7 g/l of a detergent of the invention.
  • Such process preferably is carried out by using water of a temperature in the range of from 20 °C to 35 °C, more preferred from 20 °C to 30 °C.
  • Such process also preferably is carried out by applying manual force to the laundry immersed in the laundry liquor for a period of from 5 minutes to 20 minutes, more preferred from 5 minutes to 10 minutes.
  • the laundry may be treated as is usual for other washing processes, that is it may be rinsed with water once or several times, a fabric softener may be applied to it, and the laundered items may be dried.
  • a detergent according to the present invention contains by preference peroxygen-based bleaching agents, in particular in quantities in the range from 5 wt % to 70 wt %, as well as (if applicable) bleach activator, in particular in quantities in the range from 2 wt % to 10 wt %.
  • the suitable bleaching agents are, by preference, the peroxygen compounds usually used in laundry detergents, such as percarboxylic acids, for example diperdodecanoic acid or phthaloylaminoper-oxycaproic acid, hydrogen peroxide, alkali perborate that can be present as a tetra- or monohydrate, percarbonate, perpyrophosphate, and persilicate, which as a rule are present as alkali salts, in particular as sodium salts.
  • percarboxylic acids for example diperdodecanoic acid or phthaloylaminoper-oxycaproic acid
  • hydrogen peroxide alkali perborate that can be present as a tetra- or monohydrate
  • percarbonate perpyrophosphate
  • persilicate which as a rule are present as alkali salts, in particular as sodium salts.
  • Bleaching agents of this kind are present, in laundry detergents that contain a cellulose derivative used according to the present invention, by preference in quantities of up to 25 wt %, in particular up to 15 wt %, and particularly preferably from 5 wt % to 15 wt %, based in each case on the entire detergent, percarbonate being used in particular.
  • the optionally present component of bleach activators encompasses the N- or O-acyl compounds usually utilized, for example multiply acylated alkylenediamines, in particular tetraacetylethylenediamine, acylated glycourils, in particular tetraacetyl glycouril, N-acylated hydantoins, hydrazides, triazoles, urazoles, diketopipera-zines, sulfuryl amides, and cyanurates, also carboxylic acid anhydrides, in particular phthalic acid anhydride, carboxylic acid esters, in particular sodium isononanoyl phenolsulfonate, and acylated sugar derivatives, in particular pentaacetyl glucose, as well as cationic nitrile derivatives such as trimethylammonium acetonitrile salts.
  • N- or O-acyl compounds usually utilized for example multiply acylated alkylenediamines, in particular tetraacety
  • the bleach activators can in known fashion have been coated with encasing substances or granulated; tetraacetylethylenediamine granulated with the aid of carboxymethyl cellulose and having average particle sizes from 0.01 mm to 0.8 mm, granulated 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine, and/or trialkylammonium acetonitriles are particularly preferred.
  • Such bleach activators are contained in laundry detergents by preference in quantities of up to 8 wt %, in particular from 2 wt % to 6 wt %, based in each case on the entire detergent.
  • a detergent according to the present invention used according to the present invention, or utilized in the method according to the present invention contains nonionic surfactant, selected from fatty alkylpolyglycosides, fatty alkylpolyalkoxylates, in particular-ethoxylates and/or -propoxylates, fatty acid polyhydroxyamides and/or ethoxylation and/or propoxylation products of fatty alkyl amines, vicinal diols, fatty acid alkyl esters, and/or fatty acid amides, as well as mixtures thereof, in particular in a quantity in the range from 2 wt % to 25 wt %.
  • nonionic surfactant selected from fatty alkylpolyglycosides, fatty alkylpolyalkoxylates, in particular-ethoxylates and/or -propoxylates, fatty acid polyhydroxyamides and/or ethoxylation and/or propoxylation products of fatty alkyl amines
  • a further embodiment of such detergents encompasses the presence of synthetic anionic surfactant of the sulfate and/or sulfonate type, in particular fatty alkyl sulfate, fatty alkyl ether sulfate, sulfo-fatty acid ester, and/or sulfo-fatty acid di-salts, in particular in a quantity in the range from 2 wt % to 25 wt %.
  • the anionic surfactant is preferably selected from the alkyl or alkenyl sulfates and/or the alkyl or alkenyl ether sulfates in which the alkyl or alkenyl group possesses 8 to 22, in particular 12 to 18 carbon atoms. These usually are not individual substances, but rather cuts or mixtures. Preferred among them are those whose proportion of compounds having longer-chain groups in the range from 16 to 18 carbon atoms is above 20 wt %.
  • nonionic surfactants are the alkoxylates, in particular ethoxylates and/or propoxylates, of saturated or mono- to polyunsaturated linear or branched-chain alcohols having 10 to 22 carbon atoms, by preference 12 to 18 carbon atoms.
  • the degree of alkoxylation of the alcohols is as a rule between 1 and 20, by preference between 3 and 10. They can be manufactured, in known fashion, by reacting the corresponding alcohols with the corresponding alkylene oxides.
  • the derivatives of the fatty alcohols are particularly suitable, although their branched-chain isomers, in particular so-called oxo alcohols, can also be used to manufacture usable alkoxylates.
  • the alkoxylates in particular the ethoxylates, of primary alcohols having linear, in particular dodecyl, tetradecyl, hexadecyl, or octadecyl radicals, and mixtures thereof, are accordingly usable. Also usable are corresponding alkoxylation products of alkylamines, vicinal diols, and carboxylic acid amides that correspond to the aforesaid alcohols in terms of the alkyl portion. Additionally suitable are the ethyleneoxide and/or propylene-oxide insertion products of fatty acid alkyl esters, as well as fatty acid polyhydroxyamides.
  • alkylpolyglycosides suitable for incorporation into the detergents according to the present invention are compounds of the general formula (G) n -OR 12 , in which R 12 denotes an alkyl or alkenyl radical having 8 to 22 carbon atoms, G denotes a glycose unit, and n denotes a number between 1 and 10.
  • the glycoside component (G)n refers to oligomers or polymers from naturally occurring aldose or ketose monomers, among which are included, in particular, glucose, mannose, fructose, galactose, talose, gulose, altrose, allose, idose, ribose, arabinose, xylose, and lyxose.
  • the oligomers made up of glycosidically linked monomers of this kind are characterized not only by the nature of the sugars contained in them but also by their number (the so-called degree of oligomerization).
  • the degree of oligomerization n constituting a magnitude to be ascertained analytically, generally assumes fractional numerical values; its value is between 1 and 10, below 1.5 for the glycosides used by preference, in particular between 1.2 and 1.4. Because of its good availability, glucose is a preferred monomer module.
  • the alkyl or alkenyl portion R 12 of the glycosides preferably derives likewise from easily accessible derivatives of renewable raw materials, in particular from fatty alcohols, although their branched-chain isomers, in particular so-called oxo alcohols, can also be used for the manufacture of usable glycosides.
  • the primary alcohols having linear octyl, decyl, dodecyl, tetradecyl, hexadecyl, or octadecyl radicals, and mixtures thereof, are accordingly usable.
  • Nonionic surfactant is contained in detergents according to the present invention, that are used according to the present invention, or that are utilized in the method according to the present invention, by preference in quantities from 1 wt % to 30 wt %, in particular from 1 wt % to 25 wt %; quantities in the upper part of this range are more likely to be encountered in liquid laundry detergents, and particulate laundry detergents preferably contain rather smaller quantities of up to 5 wt %.
  • the detergents can, instead or additionally, contain further surfactants, by preference synthetic anionic surfactants of the sulfate or sulfonate type, such as e.g. alkyl benzenesulfonates, in quantities by preference not above 20 wt %, in particular from 0.1 wt % to 18 wt %, based in each case on the entire detergent.
  • synthetic anionic surfactants that may be mentioned as particularly suitable for use in such detergents are the alkyl and/or alkenyl sulfates, having 8 to 22 carbon atoms, which carry an alkali-, ammonium-, or alkyl- or hydroxyalkyl-substituted ammonium ion as counter-cation.
  • the derivatives of the fatty alcohols having, in particular, 12 to 18 carbon atoms, and their branched-chain analogs are preferred.
  • the alkyl and alkenyl sulfates can be manufactured in known fashion by reacting the corresponding alcohol component with a usual sulfating reagent, in particular sulfur trioxide or chlorosulfonic acid, and subsequent neutralization with alkali-, ammonium-, or alkyl- or hydroxyalkyl-substituted ammonium bases.
  • a usual sulfating reagent in particular sulfur trioxide or chlorosulfonic acid
  • Such ether sulfates contain by preference 2 to 30, in particular 4 to 10 ethylene glycol groups per molecule.
  • suitable anionic surfactants of the sulfonate type are the ⁇ -sulfo esters obtainable by reacting fatty acid esters with sulfur trioxide and subsequent neutralization, in particular the sulfonation products deriving from fatty acids having 8 to 22 carbon atoms, by preference 12 to 18 carbon atoms, and linear alcohols having 1 to 6 carbon atoms, by preference 1 to 4 carbon atoms, and the sulfo-fatty acids generated therefrom by formal saponification.
  • soaps saturated fatty acid soaps such as the salts of lauric acid, myristic acid, palmitic acid, or stearic acid, as well as soaps derived from natural fatty acid mixtures, for example coconut, palm-kernel, or tallow fatty acids, are suitable.
  • Those soap mixtures that are made up of 50 wt % to 100 wt % saturated C12 to C18 fatty acid soaps and up to 50 wt % oleic acid soap are particularly preferred. Soap is contained by preference in quantities from 0.1 wt % to 5 wt %. Greater quantities of soap, as a rule up to 20 wt %, can, however, also be contained in particular in liquid detergents that contain a polymer used according to the present invention.
  • the detergents can also contain betaines and/or cationic surfactants, which are used (if present) by preference in quantities from 0.5 wt % to 7 wt %.
  • esterquats are particularly preferred.
  • Esterquats are quaternized fatty acid triethanolamine ester salts that conform to formula (I): in which R 1 CO denotes an acyl radical having 6 to 22 carbon atoms, R 2 and R 3 , mutually independently, denote hydrogen or R 1 CO, R 4 denotes an alkyl radical having 1 to 4 carbon atoms or a (CH 2 CH 2 O) q H group, m, n, and p in total denote 0 or numbers from 1 to 12, q denotes numbers from 1 to 12, and X - denotes a charge-equalizing anion such as a halide, alkyl sulfate, or alkyl phosphate.
  • esterquats that can be used in the context of the invention are products based on hexanoic acid, octanoic acid, decanoic acid, lauric acid, myristic acid, palmitic acid, isostearic acid, stearic acid, oleic acid, elaidic acid, arachidic acid, behenic acid, and erucic acid, and technical mixtures thereof, such as those occurring upon high-pressure cleavage of natural fats and oils.
  • technical C 12/18 coconut oil fatty acids and in particular partially hardened C 16/18 tallow or palm oil fatty acids, as well as elaidic-acid-rich C16/18 fatty acid cuts, are used.
  • the fatty acids and the triethanolamine can be used at a molar ratio from 1.1:1 to 3:1; a utilization ratio from 1.2:1 to 2.2:1, by preference 1.5:1 to 1.9:1, has proven particularly advantageous.
  • the esterquats preferred for use represent technical mixtures of mono-, di-, and triesters having an average degree of esterification from 1.5 to 1.9 and are derived from technical C 16/18 tallow or palm fatty acid (iodine number 0 to 40).
  • esterquats in addition to the quaternized carboxylic acid triethanolamine ester salts, are quaternized ester salts of carboxylic acids with diethanolalkylamines, of formula (II): in which R 1 CO denotes an acyl radical having 6 to 22 carbon atoms, R 2 denotes hydrogen or R 1 CO, R 4 and R 5 , mutually independently, denote alkyl radicals having 1 to 4 carbon atoms, m and n in total denote 0 or numbers from 1 to 12, and X denotes a charge-equalizing anion such as halide, alkyl sulfate, or alkyl phosphate.
  • R 1 CO denotes an acyl radical having 6 to 22 carbon atoms
  • R 2 denotes hydrogen or R 1 CO
  • R 4 and R 5 mutually independently, denote alkyl radicals having 1 to 4 carbon atoms
  • m and n in total denote 0 or numbers from 1 to 12
  • X denote
  • esterquats that may be mentioned are the quaternized ester salts of carboxylic acids with 1,2-dihydroxypropyldialkylamines, of formula (III): in which R 1 CO denotes an acyl radical having 6 to 22 carbon atoms, R 2 denotes hydrogen or R 1 CO, R 4 , R 6 , and R 7 , mutually independent, denote alkyl radicals having 1 to 4 carbon atoms, m and n in total denote 0 or numbers from 1 to 12, and X - denotes a charge-equalizing anion such as halide, alkyl sulfate, or alkyl phosphate.
  • R 1 CO denotes an acyl radical having 6 to 22 carbon atoms
  • R 2 denotes hydrogen or R 1 CO
  • R 4 , R 6 , and R 7 mutually independent
  • m and n in total denote 0 or numbers from 1 to 12
  • esterquats are usually brought to market in the form of 50- to 90-weight-percent alcohol solutions, which can also be diluted with water without difficulty; ethanol, propanol, and isopropanol are the usual alcohol solvents.
  • detergents according to the inventions are those that comprise 14 % by weight to 17 % by weight, preferably 15.3 % by weight, of surfactant, preferably anionic surfactant, 0.09 % by weight to 0.2 % by weight of said polyethylene oxide), 0.002 % by weight to 0.01 % by weight of fumed silica, and/or up to 0.006 % by weight, preferably 0.001 % by weight to 0.005 % by weight, of calcium salt.
  • surfactant preferably anionic surfactant, 0.09 % by weight to 0.2 % by weight of said polyethylene oxide
  • 0.002 % by weight to 0.01 % by weight of fumed silica and/or up to 0.006 % by weight, preferably 0.001 % by weight to 0.005 % by weight, of calcium salt.
  • the detergents may contain water-soluble and/or water-insoluble builders, selected in particular from alkali aluminosilicate, crystalline alkali silicate having a modulus above 1, monomeric polycarboxylate, polymeric polycarboxylate, and mixtures thereof, in particular in quantities in the range from 2.5 wt % to 60 wt %.
  • the detergent contains by preference 20 wt % to 55 wt % water-soluble and/or water-insoluble organic and/or inorganic builders.
  • water-soluble organic builder substances include, in particular, those from the class of the polycarboxylic acids, in particular citric acid and sugar acids, as well as the polymeric (poly)carboxylic acids, in particular the polycarboxylates, accessible by oxidation of polysaccharides, of International Patent Application WO 93/16110 , polymeric acrylic acids, methacrylic acids, maleic acids, and mixed polymers thereof, which can also contain small proportions of polymerizable substances, without carboxylic acid functionality, polymerized in.
  • the relative molecular weight of the homopolymers of unsaturated carboxylic acids is generally between 5000 and 200,000, that of the copolymers between 2000 and 200,000, by preference 50,000 to 120,000, based on free acid.
  • a particularly preferred acrylic acid/maleic acid copolymer has a relative molecular weight from 50,000 to 100,000.
  • Suitable, although less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers such as vinylmethyl ethers, vinyl esters, ethylene, propylene, and styrene, in which the proportion of acid is at least 50 wt %.
  • Terpolymers that contain as monomers two carboxylic acids and/or salts thereof, and vinyl alcohol and/or a vinyl alcohol derivative or a carbohydrate as a third monomer can also be used as water-soluble organic builder substances.
  • the first acid monomer or salt thereof is derived from a monoethylenically unsaturated C 3 to C 8 carboxylic acid and by preference from a C 3 to C 4 monocarboxylic acid, in particular from (meth)acrylic acid.
  • the second acid monomer or salt thereof can be a derivative of a C 4 to Ca dicarboxylic acid, maleic acid being particularly preferred.
  • the third monomeric unit is constituted in this case by vinyl alcohol and/or preferably an esterified vinyl alcohol.
  • Vinyl alcohol derivatives that represent an ester of short-chain carboxylic acids, for example of C 1 to C 4 carboxylic acids, with vinyl alcohol, are particularly preferred.
  • Preferred terpolymers contain 60 wt % to 95 wt %, in particular 70 wt % to 90 wt %, (meth)acrylic acid or (meth)acrylate, particularly preferably acrylic acid or acrylate, and maleic acid or maleinate, as well as 5 wt % to 40 wt %, by preference 10 wt % to 30 wt % vinyl alcohol and/or vinyl acetate.
  • the second acid monomer or salt thereof can also be a derivative of an allyl sulfonic acid that is substituted in the 2-position with an alkyl radical, by preference with a C 1 to C 4 alkyl radical, or with an aromatic radical that is preferably derived from benzene or benzene derivatives.
  • Preferred terpolymers contain 40 wt % to 60 wt %, in particular 45 to 55 wt %, (meth)acrylic acid or (meth)acrylate, particularly preferably acrylic acid or acrylate, 10 wt % to 30 wt %, by preference 15 wt % to 25 wt % methallyl sulfonic acid or methallyl sulfonate, and as a third monomer 15 wt % to 40 wt %, by preference 20 wt % to 40 wt % of a carbohydrate.
  • This carbohydrate can be, for example, a mono-, di-, oligo-, or polysaccharide, mono-, di-, or oligosaccharides being preferred; sucrose is particularly preferred.
  • the use of the third monomer is presumed to incorporate into the polymer defined break points that are responsible for the polymer's good biodegradability.
  • These terpolymers generally have a relative molecular weight between 1000 and 200,000, by preference between 200 and 50,000, and in particular between 3000 and 10,000.
  • Especially for the manufacture of liquid detergents they can be used in the form of aqueous solutions, by preference in the form of 30- to 50-weight-percent aqueous solutions. All the aforesaid polycarboxylic acids are used as a rule in the form of their water-soluble salts, in particular their alkali salts.
  • Organic builder substances of this kind are contained by preference in quantities of up to 40 wt %, particularly up to 25 wt %, and particularly preferably from 1 wt % to 5 wt %. Quantities close to the aforesaid upper limit are used by preference in pasty or liquid, in particular water-containing, detergents.
  • Crystalline or amorphous alkali aluminosilicates may be used in particular as water-insoluble, water-dispersible inorganic builder materials, in quantities of up to 50 wt %, by preference not above 40 wt %, and in liquid detergents in particular from 1 wt % to 5 wt %.
  • the crystalline aluminosilicates of laundry-detergent quality in particular zeolite NaA and if applicable NaX, are preferred. Quantities close to the aforesaid upper limit are used by preference in solid, particulate detergents.
  • Suitable aluminosilicates comprise, in particular, no particles having a particle size above 30 ⁇ m, and by preference comprise at least 80 wt % of particles having a size below 10 ⁇ m. Their calcium binding ability is in the range from 100 to 200 mg CaO per gram.
  • Suitable substitutes or partial substitutes for the aforesaid aluminosilicates are crystalline alkali silicates, which can be present alone or mixed with amorphous silicates.
  • the alkali silicates usable in the detergents as detergency builders have by preference a molar ratio of alkali oxide to SiO 2 below 0.95, in particular from 1:1.1 to 1:12, and can be present in amorphous or crystalline fashion.
  • Preferred alkali silicates are the sodium silicates, in particular the amorphous sodium silicates, having a Na 2 O:SiO 2 molar ratio from 1:2 to 1 :2.8.
  • Amorphous alkali silicates of this kind are obtainable commercially, for example, under the name Portil ® . They are added in the context of manufacture preferably as a solid, and not in the form of a solution.
  • Preferred crystalline sheet silicates are those in which x in the aforesaid general formula assumes the values 2 or 3.
  • both ⁇ - and ⁇ -sodium disilicates Na 2 Si 2 O 5 ⁇ y H 2 O
  • the alkali silicate content of the detergent is by preference 1 wt % to 50 wt %, and in particular 5 wt % to 35 wt %, based on anhydrous active substance. If alkali aluminosilicate, in particular zeolite, is also present as an additional builder substance, the alkali silicate content is by preference 1 wt % to 15 wt %, and in particular 2 wt % to 8 wt %, based on anhydrous active substance.
  • the weight ratio of aluminosilicate to silicate, based in each case on anhydrous active substances is then by preference 4:1 to 10:1. In detergents that contain both amorphous and crystalline alkali silicates, the weight ratio of amorphous alkali silicate to crystalline alkali silicate is by preference 1:2 to 2:1, and in particular 1:1 to 2:1.
  • further water-soluble or water-insoluble inorganic substances can be contained in the detergents according to the present invention, that are to be used according to the present invention, or that are utilized in methods according to the present invention.
  • the alkali carbonates, alkali hydrogen carbonates, and alkali sulfates, and mixtures thereof, are suitable in this context.
  • Additional inorganic material of this kind can be present in quantities of up to 70 wt %.
  • the detergents can contain further constituents that are usual in laundry detergents and cleaning agents. Included among these optional constituents are, in particular, enzymes, enzyme stabilizers, complexing agents for heavy metals, for example aminopolycarboxylic acids, amino-hydroxypolycarboxylic acids, polyphosphonic acids, and/or aminopolyphosphonic acids, foam inhibitors, for example organopolysiloxanes or paraffins, solvents, and optical brighteners, for example stilbenedisulfonic acid derivatives.
  • enzymes for example aminopolycarboxylic acids, amino-hydroxypolycarboxylic acids, polyphosphonic acids, and/or aminopolyphosphonic acids
  • foam inhibitors for example organopolysiloxanes or paraffins
  • solvents for example stilbenedisulfonic acid derivatives.
  • optical brighteners in particular compounds from the class of the substituted 4,4'-bis(2,4,6-tri-amino-s-triazinyl)stilbene-2,2'-disulfonic acids, up to 5 wt %, in particular 0.1 wt % to 2 wt % complexing agents for heavy metals, in particular aminoalkylenephosphonic acids and salts thereof, and up to 2 wt %, in particular 0.1 wt % to 1 wt % foam inhibitors, are contained in detergents according to the present invention or that are used according to the present invention, the aforesaid weight proportions referring here and in each other case to the entire detergent.
  • Solvents which can be used in particular with liquid detergents, are (in addition to water) preferably those that are miscible with water. Included among these are the lower alcohols, for example ethanol, propanol, isopropanol, and the isomeric butanols, glycerol, lower glycols, for example ethylene glycol and propylene glycol, and the ethers derivable from the aforesaid classes of compounds.
  • Enzymes that may be present are by preference selected from the group encompassing protease, amylase, lipase, cellulase, hemicellulase, oxidase, peroxidase, or mixtures thereof.
  • Protease recovered from microorganisms such as bacteria or fungi, is especially suitable.
  • Proteases are obtainable commercially, for example, under the names BLAP ® , Savinase ® , Esperase ® , Maxatase ® , Optimase ® , Alcalase ® , Durazym ® , or Maxapem ® .
  • Usable lipases may be recovered from Humicola lanuginosa, from Bacillus species, from Pseudomonas species, from Fusarium species, from Rhizopus species, or from Aspergillus species. Suitable lipases are obtainable commercially, for example, under the names Lipolase ® , Lipozym ® , Lipomax ® , Lipex ® , Amano ® Lipase, Toyo-Jozo ® Lipase, Meito ® Lipase, and Diosynth ® Lipase.
  • Suitable amylases are commercially available, for example, under the names Maxamyl ® , Termamyl ® , Duramyl ® , and Purafect ® OxAm.
  • Usable cellulases are recoverable from bacteria or fungi, which exhibits a pH optimum preferably in the weakly acid to weakly alkaline range from 6 to 9.5.
  • Cellulases of this kind are commercially available under the names Celluzyme ® , Carezyme ® , and Ecostone ® .
  • aminoalcohols for example mono-, di-, triethanol- and -propanolamine and mixtures thereof, lower carboxylic acids, boric acid or alkali borates, boric acid/carboxylic acid combinations, boric acid esters, boronic acid derivatives, and/or sulfur-containing reducing agents.
  • foam inhibitors include long-chain soaps, in particular behenic soap, fatty acid amides, paraffins, waxes, microcrystalline waxes, organopolysiloxanes, and mixtures thereof, which can furthermore contain microfine, optionally silanized or otherwise hydrophobized silicic acid.
  • foam inhibitors of this kind are preferably bound to granular, water-soluble carrier substances as described.
  • the detergent is particulate, and contains up to 25 wt %, in particular 5 wt % to 20 wt % bleaching agent, in particular alkali percarbonate, up to 15 wt %, in particular 1 wt % to 10 wt % bleach activator, 20 wt % to 55 wt % inorganic builders, up to 10 wt %, in particular 2 wt % to 8 wt % water-soluble organic builders, 10 wt % to 25 wt % synthetic anionic surfactant, 1 wt % to 5 wt % nonionic surfactant, and up to 25 wt %, in particular 0.1 wt % to 25 wt % inorganic salts, in particular alkali carbonate and/or alkali hydrogen carbonate.
  • a detergent into which cellulose derivative to be used according to the present invention is incorporated is liquid, and contains 10 wt % to 25 wt %, in particular 12 wt % to 22.5 wt % nonionic surfactant, 2 wt % to 10 wt %, in particular 2.5 wt % to 8 wt % synthetic anionic surfactant, 3 wt % to 15 wt %, in particular 4.5 wt % to 12.5 wt % soap, 0.5 wt % to 5 wt %, in particular 1 wt % to 4 wt % organic builders, in particular polycarboxylate such as citrate, up to 1.5 wt %, in particular 0.1 wt % to 1 wt % complexing agents for heavy metals, such as phosphonate, and in addition to an optionally contained enzyme, enzyme stabilizer, dye and/or fragrance, water and/or water-miscible solvent.
  • heavy metals such as
  • polyester-active soil-release-enabling polymer made up of a dicarboxylic acid and an optionally polymeric diol, to intensify the cleaning performance of bleaching-agent-containing laundry detergents when washing textiles.
  • a polyester-active soil-release-enabling polymer are also possible in the context of detergents according to the present invention and of the method according to the present invention.
  • soil-release-enabling polymers known to be polyester-active, are copolyesters of dicarboxylic acids, for example adipic acid, phthalic acid, or terephthalic acid, diols, for example ethylene glycol or propylene glycol, and polydiols, for example polyethylene oxide.
  • dicarboxylic acids for example adipic acid, phthalic acid, or terephthalic acid
  • diols for example ethylene glycol or propylene glycol
  • polydiols for example polyethylene oxide.
  • soil-release-enabling polyesters preferred for use are those compounds that are accessible formally by the esterification of two monomer parts, the first monomer being a dicarboxylic acid HOOC-Ph-COOH and the second monomer being a diol HO-(CHR 11 -) a OH, which can also be present as a polymeric diol H-(O-(CHR 11 -) a ) b OH, in which Ph denotes an o-, m-, or p-phenylene radical that can carry 1 to 4 substituents selected from alkyl radicals having 1 to 22 carbon atoms, sulfonic acid groups, carboxyl groups, and mixtures thereof, R 11 denotes hydrogen, an alkyl radical having 1 to 22 carbon atoms, and mixtures thereof, a is a number from 2 to 6, and b is a number from 1 to 300.
  • Ph denotes an o-, m-, or p-phenylene radical that can carry 1 to 4
  • both monomer diol units -O-(CHR 11 -) a ) b O- and polymer diol units -(O-(CHR 11 -) a ) b O- are present in the polyesters obtainable therefrom.
  • the molar ratio of monomer diol units to polymer diol units is by preference 100:1 to 1:100, in particular 10:1 to 1:10.
  • the degree of polymerization b is preferably in the range from 4 to 200, in particular from 12 to 140.
  • the molecular weight or average molecular weight, or the maximum of the molecular weight distribution, of preferred soil-release-enabling polyesters is in the range from 250 to 100,000, in particular from 500 to 50,000.
  • the acid on which the Ph radical is based is selected by preference from terephthalic acid, isophthalic acid, phthalic acid, trimellitic acid, mellitic acid, the isomers of sulfophthalic acid, sulfoisophthalic acid, and sulfoterephthalic acid, and mixtures thereof. If their acid groups are not part of the ester bonds in the polymer, they are preferably present in salt form, in particular as an alkali or ammonium salt. Among these, the sodium and potassium salts are particularly preferred.
  • small proportions - in particular no more than 10 mol % based on the proportion of Ph having the meaning indicated above - of other acids that comprise at least two carboxyl groups can be contained in the soil-release-enabling polyester. Included among these are, for example, alkylene and alkenylene dicarboxylic acids such as malonic acid, succinic acid, fumaric acid, maleic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, and sebacic acid.
  • alkylene and alkenylene dicarboxylic acids such as malonic acid, succinic acid, fumaric acid, maleic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, and sebacic acid.
  • HO-(CHR 11 -) a OH include those in which R 11 is hydrogen and a is a number from 2 to 6, and those in which a has the value of 2 and R 11 is selected from hydrogen and the alkyl radicals having 1 to 10, in particular 1 to 3, carbon atoms.
  • R 11 is hydrogen and a is a number from 2 to 6
  • R 11 is selected from hydrogen and the alkyl radicals having 1 to 10, in particular 1 to 3, carbon atoms.
  • those of the formula HO-CH2-CHR 11 -OH, in which R 11 has the meaning indicated above are particularly preferred.
  • diol components are ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1,2-decanediol, 1,2-dodecanediol, and neopentyl glycol.
  • Polyethylene glycol having an average molar weight in the range from 1000 to 6000 is particularly preferred among the polymeric diols.
  • the polyesters having the composition as described above can also be end-capped, alkyl groups having 1 to 22 carbon atoms and esters of monocarboxylic acids being suitable as terminal groups.
  • the terminal groups, bound via ester bonds, can be based on alkyl, alkenyl, and aryl monocarboxylic acids having 5 to 32 carbon atoms, in particular 5 to 18 carbon atoms.
  • valeric acid hexanoic acid, oenanthic acid, octanoic acid, pelargonic acid, decanoic acid, undecanoic acid, undecenoic acid, lauric acid, lauroleic acid, tridecanoic acid, myristic acid, myristoleic acid, pentadecanoic acid, palmitic acid, stearic acid, petroselic acid, petroselaidic acid, oleic acid, linoleic acid, linolaidic acid, linolenic acid, eleostearic acid, arachidic acid, gadoleic acid, arachidonic acid, behenic acid, erucic acid, brassidic acid, clupanodonic acid, lignoceric acid, cerotic acid, melissic acid, benzoic acid, that can carry 1 to 5 substituents having a total of up to 25 carbon atoms, in particular 1 to 12 carbon
  • the terminal groups can also be based on hydroxymonocarboxylic acids having 5 to 22 carbon atoms, included among which are, for example, hydroxyvaleric acid, hydroxyhexanoic acid, ricinoleic acid, its hydrogenation product hydroxystearic acid, and o-, m-, and p-hydroxybenzoic acid.
  • the hydroxymonocarboxylic acids can in turn be connected to one another via their hydroxyl group and their carboxyl group, and thus be present more than once in a terminal group.
  • the number of hydroxymonocarboxylic acid units per terminal group i.e. their degree of oligomerization, is in the range from 1 to 50, in particular from 1 to 10.
  • polymers of ethylene terephthalate and polyethylene oxide terephthalate in which the polyethylene glycol units have molecular weights from 750 to 5000 and the molar ratio of ethylene terephthalate to polyethylene oxide terephthalate is 50:50 to 90:10, are used.
  • the soil-release-enabling polymers are preferably water-soluble; the term "water-soluble” is to be understood as a solubility of at least 0.01 g, by preference at least 0.1 g of the polymer per liter of water at room temperature and pH 8. Polymers preferred for use exhibit under these conditions, however, a solubility of at least 1 g per liter, in particular at least 10 g per liter.
  • Solid detergents according to the present invention (D1 and D2) and a comparative detergent (C1) were prepared by mixing the ingredients given in the following table 1 in the amounts also given there.
  • Table 1 Detergent compositions [wt %] D1 D2 C1 Sodium ABS 15.3 15.3 15.3 Sodium carbonate 20 20 20 Sodium silicate 5.9 5.9 5.9 Sodium HEDP 0.3 0.3 0.3 CMC 0.3 0.3 0.3 Perfume 0.25 0.25 0.25 Dye 0.155 0.155 0.155 Sodium sulfate 53 53 53 Polyethylene oxide), Mw 5,000,000 g/mol 0.095 0.19 0 fumed silica 0.003 0.006 0 calcium sulfate / calcium carbonate 0.002 0.004 0 Water ad 100
EP23156278.6A 2022-03-07 2023-02-13 Détergent pour lessive Pending EP4242287A1 (fr)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4844821A (en) * 1988-02-10 1989-07-04 The Procter & Gamble Company Stable liquid laundry detergent/fabric conditioning composition
WO1993016110A1 (fr) 1992-02-11 1993-08-19 Henkel Kommanditgesellschaft Auf Aktien Procede de fabrication de polycarboxylates a base de polysaccharides
WO2000017299A1 (fr) * 1998-09-21 2000-03-30 The Procter & Gamble Company Agglomerats d'adjuvants pour detergents a lessive en poudre
US20050192199A1 (en) * 2003-03-24 2005-09-01 Cartwright Brian K. Cleaner with soil flocculant
WO2019045958A1 (fr) * 2017-09-04 2019-03-07 Dow Global Technologies Llc Formulation de détergent à lessive en poudre

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4844821A (en) * 1988-02-10 1989-07-04 The Procter & Gamble Company Stable liquid laundry detergent/fabric conditioning composition
WO1993016110A1 (fr) 1992-02-11 1993-08-19 Henkel Kommanditgesellschaft Auf Aktien Procede de fabrication de polycarboxylates a base de polysaccharides
WO2000017299A1 (fr) * 1998-09-21 2000-03-30 The Procter & Gamble Company Agglomerats d'adjuvants pour detergents a lessive en poudre
US20050192199A1 (en) * 2003-03-24 2005-09-01 Cartwright Brian K. Cleaner with soil flocculant
WO2019045958A1 (fr) * 2017-09-04 2019-03-07 Dow Global Technologies Llc Formulation de détergent à lessive en poudre

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DDP SPECIALTY ELECTRONIC MATERIALS US: "UCARFLOC 309CP Polymer, SAFETY DATA SHEET", 15 October 2018 (2018-10-15), pages 1 - 10, XP009543347, Retrieved from the Internet <URL:https://www.chempoint.com/products/dupont/polyox-water-soluble-resins/polyox-ucarfloc/309cp> [retrieved on 20230712] *

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