EP4239049A1 - Coefficient d'efflorescence - Google Patents

Coefficient d'efflorescence Download PDF

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Publication number
EP4239049A1
EP4239049A1 EP22160242.8A EP22160242A EP4239049A1 EP 4239049 A1 EP4239049 A1 EP 4239049A1 EP 22160242 A EP22160242 A EP 22160242A EP 4239049 A1 EP4239049 A1 EP 4239049A1
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EP
European Patent Office
Prior art keywords
weight
blooming
washing
perfume composition
oil
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
EP22160242.8A
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German (de)
English (en)
Inventor
Andreas Bauer
Andreas Gerigk
Hubert Smyrek
Manuela Materne
Christian GIESEN
Lisa RULAND
Frank Pessel
Malte BRUTSCHY
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
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to EP22160242.8A priority Critical patent/EP4239049A1/fr
Priority to PCT/EP2023/054771 priority patent/WO2023165910A1/fr
Publication of EP4239049A1 publication Critical patent/EP4239049A1/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
    • C11D3/50Perfumes
    • C11D2111/12

Definitions

  • the invention relates to a perfume composition which comprises at least one fragrance with a blooming coefficient (Bc) of ⁇ 0.5.
  • the invention also relates to detergents or cleaning agents which comprise the perfume composition according to the invention and the use of the compositions or agents according to the invention for washing textiles or for cleaning surfaces and/or for scenting the room in which the composition or agent is used.
  • the invention also relates to a method for washing textiles or cleaning surfaces and/or for scenting the room in which the method is carried out, a perfume composition according to the invention or a detergent or cleaning agent according to the invention being used in at least one method step.
  • the consumer When using detergents or cleaning agents, the consumer expects not only long-lasting olfactory performance after using the product on the surface, e.g. on the textile, but also a space-filling perfume effect during or after using a product.
  • This can, for example, be a room-filling effect when drying textiles on the line, when opening the washing machine after the wash cycle or the room-filling effect after cleaning floor surfaces.
  • This room-filling (perfume) effect is also known as the blooming effect and is defined by an improved perception and intensity of perfumes in the room during or after the use of products that contain this perfume.
  • fragrances with a specific blooming coefficient can influence the space-filling effect of a perfume composition.
  • this effect can be significantly improved taking into account certain concentrations of these fragrances in the perfume composition. This effect can be observed both during application and after application.
  • a first aspect of the invention thus relates to a perfume composition
  • the perfume composition preferably contains the at least one fragrance with a blooming coefficient of ⁇ 0.5 in a concentration of at least 1% by weight, more preferably at least 5% by weight, even more preferably at least 10% by weight, even more preferably at least 15% by weight, more preferably at least 20% by weight, and especially at least 25% by weight, based on the total weight of the perfume composition.
  • a further aspect of the invention relates to a washing or cleaning agent comprising a perfume composition according to the invention.
  • the invention preferably relates to the use of the perfume composition according to the invention or the washing or cleaning agent according to the invention for washing textiles or for cleaning surfaces and at the same time for scenting the room in which the composition or the agent is used.
  • the invention preferably relates to a method for washing textiles or for cleaning surfaces and at the same time for scenting the room in which the method is carried out, characterized in that a perfume composition according to the invention or a washing or cleaning agent according to the invention is used in at least one method step.
  • the number average molar mass can be determined, for example, by means of gel permeation chromatography (GPC) in accordance with DIN 55672-1:2007-08 with THF as the eluent.
  • GPC gel permeation chromatography
  • the mass-average molar mass M w can also be determined by GPC, as described for M n .
  • the expression “substantially free from” means that the respective component can in principle be contained in the composition according to the invention or the agent according to the invention, but is then present in an amount that is significantly below the amount usually required or used for the function of this component.
  • the property “substantially free from” of a specific component is therefore preferably a total amount of less than 1% by weight, more preferably less than 0.1% by weight, even more preferably less than 0.01% by weight. -%, more preferably below 0.001% by weight, especially free, i.e. below the detection limit, considered thereto, based on the total weight of the composition or agent. It can also mean that the corresponding component was not intentionally added.
  • perfume or “perfume composition” denotes individual fragrance or fragrance compounds or mixtures of several such compounds, and thus covers, for example, synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type, as well as natural fragrance mixtures , as are accessible from plant sources.
  • odorant/perfume Most people perceive the smell of an odorant/perfume as pleasant and often corresponds to the smell of, for example, blossoms, fruits, spices, bark, resin, leaves, grasses, mosses and roots. Rich substances/perfumes can also be used to mask unpleasant odors or to provide a non-smelling substance with a desired smell.
  • At least one includes but is not limited to 1, 2, 3, 4, 5, 6 and more.
  • the information refers to the type of ingredient and not to the absolute number of molecules.
  • At least one fragrance thus means, for example, at least one type of fragrance, ie one type of fragrance or a mixture of several different fragrances can be meant.
  • the information relates to all compounds of the specified type contained in the composition/mixture, ie that the composition does not contain any other compounds of this type in addition to the specified amount of the corresponding compounds.
  • the vapor pressure for generating a blooming effect is directly related to the odor threshold of each individual fragrance.
  • the vapor pressure of the fragrance at 25° C. (VP25°) is given in pascals unless otherwise described. It is a material- and temperature-dependent gas pressure and describes the ambient pressure below which a liquid begins to change into the gaseous state at a constant temperature.
  • any suitable measuring method can be used to determine the vapor pressure.
  • Exemplary measurement methods include, but are not limited to, the dynamic measurement method, in which the boiling temperature of the test substance is measured at a certain specified pressure; the statistical measurement method, in which the vapor pressure is measured that occurs in thermodynamic equilibrium in a closed system at a given temperature over a substance; the effusion method, in which the amount of substance that leaves a measuring cell per unit of time through an opening of known size is determined under vacuum conditions in such a way that a return of the substance into the measuring cell can be neglected; or the gas saturation method, in which a stream of an inert gas is passed over the test substance so as to saturate it with its vapor, the amount of substance being transported by a known amount of carrier gas being determined either by collection in a suitable trap or by an on-line analytical methods can be measured.
  • the measuring methods are to be selected according to the amount of vapor pressure to be expected.
  • the odor threshold value (GSW or ODT (odor detection threshold)) describes the minimum concentration of a gaseous, sensory active substance, for example an odorant, which a living being, for example a human being, can just barely perceive via the sense of smell. In the context of this invention, this value is given in ⁇ g/m 3 unless otherwise stated.
  • the odor threshold value can either be taken from the literature or, for example, without being limited thereto, determined by means of olfactometry, in which the odor sample is mixed with non-smelling clean air and presented to a number of test persons. Defined dilution levels of the odor sample are adhered to.
  • the blooming coefficient (Bc) can be calculated from the vapor pressure [Pa] of the fragrance at 25° C. (VP25°) and the odor threshold value [ ⁇ g/m 3 ] of the fragrance (ODT) using the above formula.
  • the perfume composition according to the invention can be a single fragrance with a blooming coefficient of ⁇ 0.5 or a mixture of two or more fragrances, for example 1, 3, 4, 5, 6, 7, 8, 9, 10 or more fragrances, each have a blooming coefficient of ⁇ 0.5.
  • the composition can additionally comprise other fragrances which have a blooming coefficient below 0.5.
  • the perfume composition contains at least 1% by weight, at least 2% by weight, at least 3% by weight, at least 4% by weight, at least 5% by weight, at least 6% by weight, at least 7 % by weight, at least 8% by weight, at least 9% by weight, at least 10% by weight, at least 11% by weight, at least 12% by weight, at least 13% by weight, at least 14% by weight %, at least 15% by weight, at least 16% by weight, at least 17% by weight, at least 18% by weight, at least 19% by weight, at least 20% by weight, at least 21% by weight.
  • -% at least 22% by weight, at least 23% by weight, at least 24% by weight or at least 25% by weight, for example ⁇ 25% by weight, ⁇ 27% by weight, ⁇ 30% by weight. %, ⁇ 35% by weight, ⁇ 40% by weight, ⁇ 45% by weight or ⁇ 50% by weight of at least one fragrance with a blooming coefficient of ⁇ 0.5, based on the total weight of the perfume composition.
  • the perfume composition contains at least 15% by weight, in particular at least 25% by weight, of at least one fragrance with a blooming coefficient of ⁇ 0.5, based on the total weight of the perfume composition.
  • the blooming coefficient of the at least one fragrance in the perfume composition has a value of ⁇ 0.6, ⁇ 0.7, ⁇ 0.8, ⁇ 0.9, ⁇ 1, ⁇ 1.5, ⁇ 2, ⁇ 3 , ⁇ 4, ⁇ 5, ⁇ 6, ⁇ 7, ⁇ 8, ⁇ 9, ⁇ 10, ⁇ 15, ⁇ 20, ⁇ 25, ⁇ 30, ⁇ 35, ⁇ 40, ⁇ 50, ⁇ 55, ⁇ 60, ⁇ 65, ⁇ 70, ⁇ 75, ⁇ 80, ⁇ 85, ⁇ 90, ⁇ 95, or ⁇ 100. If two or more fragrances are present in the perfume composition, the blooming coefficients can be (virtually) the same or differ little or else greatly.
  • the proportion of fragrances with a blooming coefficient of ⁇ 0.5 is at most 50% by weight, based on the total weight of the perfume compositions, for example at most 40% by weight, at most 35% by weight, at most 30% by weight. %, at most 25% by weight, at most 20% by weight, at most 15% by weight or at most 10% by weight.
  • the perfume compositions according to the invention contain at least two different fragrances, each of which has a blooming coefficient of ⁇ 0.5, ⁇ 0.6, ⁇ 0.7, ⁇ 0.8, ⁇ 0.9, ⁇ 1, ⁇ 1.5 , ⁇ 2, ⁇ 3, ⁇ 4, ⁇ 5, ⁇ 6, ⁇ 7, ⁇ 8, ⁇ 9, ⁇ 10, ⁇ 15, ⁇ 20, ⁇ 25, ⁇ 30, ⁇ 35, ⁇ 40, ⁇ 50, ⁇ 55, ⁇ 60, ⁇ 65, ⁇ 70, ⁇ 75, ⁇ 80, ⁇ 85, ⁇ 90, ⁇ 95, or ⁇ 100.
  • At least one fragrance of the perfume composition according to the invention can be an aldehyde, preferably selected from adoxal (2,6,10-trimethyl-9-undecenal), anisaldehyde (4-methoxybenzaldehyde), cymal (3-(4- isopropyl-phenyl)-2-methylpropanal), ethylvanillin, florhydral (3-(3-isopropylphenyl)butanal), helional (3-(3,4-methylenedioxyphenyl)-2-methylpropanal), heliotropine, hydroxycitronellal, lauraldehyde, lyral (3 - and 4-(4-Hydroxy-4-methylpentyl)-3-cyclohexene-1-carboxaldehyde), methylnonylacetaldehyde, Lilial (3-(4-tert-butylphenyl)-2-methylpropanal), phenylacetalde
  • At least one fragrance can be a ketone, preferably selected from methyl beta-naphthyl ketone, musk indanone (1,2,3,5,6,7-hexahydro-1,1,2,3,3- pentamethyl-4H-inden-4-one), tonalid (6-acetyl-1,1,2,4,4,7-hexamethyltetralin), alpha-damascone, beta-damascone, delta-damascone, iso-damascone, damascenone, Methyldihydrojasmonate, menthone, carvone, camphor, koavone (3,4,5,6,6-pentamethylhept-3-en-2-one), fenchone, alpha-lonone, beta-lonone, gamma-methyl-ionone, fleuramon (2nd -heptylcyclopentanone), dihydrojasmon, cis-jasmon,
  • a fragrance can be an alcohol, preferably selected from 10-undecen-1-ol, 2,6-dimethylheptan-2-ol, 2-methylbutanol, 2-methylpentanol, 2-phenoxyethanol, 2- Phenylpropanol, 2-tert-butylcyclohexanol, 3,5,5-trimethylcyclohexanol, 3-hexanol, 3-methyl-5-phenylpentanol, 3-octanol, 3-phenylpropanol, 4-heptenol, 4-isopropylcyclohexanol, 4 -tert-Butycyclohexanol, 6,8-dimethyl-2-nona-nol, 6-nonen-1-ol, 9-decen-1-ol, ⁇ -methylbenzyl alcohol, ⁇ -terpineol, amyl salicylate, benzyl alcohol, benzyl salicylate, ⁇ - Terpineol, amy
  • Perfume compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate (DMBCA), phenylethyl acetate, Benzyl Acetate, Ethyl Methyl Phenylglycinate, Allyl Cyclohexyl Propionate, Styrallyl Propionate, Benzyl Salicylate, Cyclohexyl Salicylate, Floramat, Melusate and Jasmacyclate.
  • DMBCA dimethylbenzylcarbinyl acetate
  • Benzyl Acetate Ethyl Methyl Phenylglycinate
  • Allyl Cyclohexyl Propionate Styrallyl Propionate
  • Benzyl Salicylate Cyclohexyl Salicylate
  • Ethers include, for example, benzyl ethyl ether and ambroxan, and hydrocarbons include primarily terpenes such as limonene and pinene. However, preference is given to using mixtures of different fragrances which together produce an appealing fragrance note.
  • a fragrance can be an essential oil, such as angelica root oil, anise oil, arnica flower oil, basil oil, bay oil, champaca flower oil, citrus oil, noble fir oil, noble pine cone oil, elemi oil, eucalyptus oil, fennel oil, pine needle oil, galbanum oil, geranium oil, ginger grass oil, guaiac oil , gurjun balm oil, helichrysum oil, ho oil, ginger oil, iris oil, jasmine oil, cajeput oil, calamus oil, chamomile oil, camphor oil, kanaga oil, cardamom oil, cassia oil, pine needle oil, copaiva balm oil, coriander oil, spearmint oil, caraway oil, cumin oil, labdanum oil, lavender oil, lemongrass oil, lime blossom oil, lime oil , Mandarin Oil, Melissa Oil, Mint Oil, Musk Seed Oil, Clary Oil, Myrrh Oil, Clove Oil, Neroli Oil, Nia
  • Suitable fragrance compounds can be found in Table 1, but all other fragrance compounds that are known to the person skilled in the art and are considered suitable by him are also included in the context of the invention, as long as at least one of the fragrance compounds in the perfume composition according to the invention has a blooming coefficient of ⁇ 0, 5 has.
  • the at least one fragrance with a blooming coefficient of ⁇ 0.5 is selected from the group consisting of manzanate, ethyl 2-methylbutyrate, ethyl butyrate, aldehyde c 07 (heptanal), isopropylmethyl 2-butyrate, hexenyl acetate, aldehyde c 06 (hexanal), neoproxen, cerezoate, aldehyde c 08 (octanal), melonal, eucalyptus oil globulus, trans-2- hexenal, prenyl acetate, romilate, (para-)cresyl methyl ether, methylhexyl ketone, ethyl acetate, pinane, sulfox, amyl propionate, koumalactone, methylbutyl -2-propionate, isopentyrate, hexanol, (beta-)hex
  • individual fragrances of the perfume composition according to the invention can be present in free form, as fragrance storage substances or in encapsulated form, without being limited thereto. Furthermore, the fragrances can be applied to certain carrier molecules. However, free fragrances are particularly preferably used.
  • the invention relates to a washing or cleaning agent comprising the perfume composition according to the invention.
  • washing or cleaning agents both concentrates and agents to be used undiluted, for use on a commercial scale, in the washing machine or for hand washing or hand cleaning.
  • detergents for textiles, carpets, or natural fibers, for which the term detergent is used.
  • detergents or cleaning agents within the scope of the invention also include washing aids that are added to the actual detergent in manual or machine washing in order to achieve a further effect.
  • detergents or cleaning agents within the scope of the invention also include textile pre-treatment and after-treatment agents, i.e. agents with which the item of laundry is brought into contact before the actual wash, for example to loosen stubborn dirt, and also agents that are in one of the actual Textile washing subsequent step give the laundry other desirable properties such as a pleasant feel, crease resistance or low static charge.
  • the latter means include fabric softeners.
  • the perfume composition according to the invention is present in the washing or cleaning agent in an amount of from 0.001 to 30% by weight, preferably from 0.01 to 20% by weight, more preferably from 0.1 to 10% by weight. in particular from 0.5 to 5% by weight, for example 1% by weight, based on the total weight of the detergent or cleaning agent.
  • washing or cleaning agent described herein can be solid or liquid.
  • the washing or cleaning agents according to the invention are preferably of a liquid nature and can in particular be in the form of homogeneous solutions or suspensions.
  • Liquid as used herein includes liquids and gels as well as pasty compositions. It is preferred that the liquid compositions are flowable and pourable at room temperature, but it is also possible for them to have a yield point.
  • Solid in this context means that the composition is present as a solid under standard conditions, in particular as a powder or granules or compactate.
  • the washing or cleaning agent is in a pre-portioned form, preferably in the form of a unit dose, e.g. encased in a water-soluble film.
  • the washing or cleaning agent can also have several spatially separate compositions, which makes it possible to separate incompatible ingredients from one another and also makes it possible to offer compositions in combination that are used at different times.
  • the washing or cleaning agent according to the invention can contain at least one additional component, preferably at least two additional components, preferably selected from the group consisting of builders, surfactants, polymers, water-miscible solvents, pH regulators, enzymes, enzyme stabilizers/ - Inhibitors, electrolytes, bleaches, bleach catalysts, bleach activators, hydrotropes, foam regulators/inhibitors, dyes, fluorescent agents, silicone oils, soil release polymers, graying inhibitors, shrinkage inhibitors, anti-crease agents, antimicrobial agents, germicides, fungicides, antioxidants, preservatives, corrosion inhibitors, antistatic agents , bittering agents, ironing aids, repellents and impregnating agents, skin care active ingredients, swelling and non-slip agents, complexing agents, softening components, UV absorbers, other fragrances or storage substances and perfume carriers, without being limited to them.
  • the use of one or more other components depends on the intended use of the washing or cleaning agent.
  • the washing or cleaning agent according to the invention can preferably have at least one other component, preferably at least two other components, selected from the group consisting of other fragrances or fragrance storage compounds, builders, surfactants, complexing agents, polymers, water-miscible solvents, pH regulators, enzymes, enzyme stabilizers/- Inhibitors, bleaches, bleach catalysts, bleach activators, foam regulators and dyes.
  • other components preferably at least two other components, selected from the group consisting of other fragrances or fragrance storage compounds, builders, surfactants, complexing agents, polymers, water-miscible solvents, pH regulators, enzymes, enzyme stabilizers/- Inhibitors, bleaches, bleach catalysts, bleach activators, foam regulators and dyes.
  • Suitable surfactants are, for example, all known nonionic, anionic, cationic, zwitterionic and amphoteric surfactants, with at least nonionic and/or anionic surfactants being used in various embodiments.
  • the agent can contain 0.5 to 50% by weight of surfactants, preferably 1 to 40% by weight, in particular 5 to 30% by weight.
  • Nonionic surfactants known to those skilled in the art can be used as nonionic surfactants.
  • Nonionic surfactants to be used with preference come from the groups of alkoxylated nonionic surfactants, in particular ethoxylated primary alcohols, and also mixtures of these surfactants with structurally complex surfactants such as polyoxypropylene/polyoxyethylene/polyoxypropylene ((PO/EO/PO) surfactants).
  • Preferred anionic surfactants are fatty alcohol sulfates, fatty alcohol ether sulfates, dialkyl ether sulfates, monoglyceride sulfates, alkyl benzene sulfonates, olefin sulfonates, alkane sulfonates, ether sulfonates, n-alkyl ether sulfonates, ester sulfonates and lignin sulfonates.
  • the anionic surfactants are preferably used as sodium salts, but can also be present as other alkali metal or alkaline earth metal salts, for example potassium or magnesium salts, and in the form of ammonium or mono-, di-, tri- or tetraalkylammonium salts, in the case of sulfonates also in the form of their corresponding acid, e.g. dodecylbenzenesulfonic acid.
  • Suitable amphoteric surfactants are, for example, betaines of the formula (R iii )(R iv )(R v )N + CH 2 COO - , in which R iii is an alkyl radical having 8 to 25, preferably 10 to 21 carbon atoms and which is optionally interrupted by heteroatoms or heteroatom groups, and R iv and R v are identical or different alkyl radicals having 1 to 3 carbon atoms, in particular C 10 -C 18 -alkyldimethylcarboxymethylbetaine and C 11 -C 17 -alkylamidopropyldimethylcarboxymethylbetaine.
  • Amine oxides for example, can be used as zwitterionic surfactants.
  • Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R vi )(R vii )(R viii )(R ix )N + X - , where R vi to R ix are four of the same or different types, in particular two long and two short-chain alkyl radicals and X - stand for an anion, in particular a halide ion, for example didecyl dimethyl ammonium chloride, alkyl benzyl didecyl ammonium chloride and mixtures thereof.
  • Suitable cationic surfactants are the quaternary surface-active compounds, in particular with a sulfonium, phosphonium, iodonium or arsonium group, which are also known as antimicrobial agents.
  • quaternary surface-active compounds with an antimicrobial effect, the agent can be designed with an antimicrobial effect or its antimicrobial effect, which may already be present due to other ingredients, can be improved.
  • a composition according to the invention preferably contains at least one water-soluble and/or water-insoluble, organic and/or inorganic builder.
  • water-soluble organics Builder substances include polycarboxylic acids, especially citric acid and sugar acids, monomeric and polymeric aminopolycarboxylic acids, especially methylglycinediacetic acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid, as well as polyaspartic acid, polyphosphonic acids, especially aminotris(methylenephosphonic acid), ethylenediaminetetrakis(methylenephosphonic acid) and 1-hydroxyethane-1,1-diphosphonic acid, polymeric hydroxy compounds such as dextrin and polymeric (poly)carboxylic acids, in particular the polycarboxylates obtainable by oxidation of polysaccharides or dextrins, polymeric acrylic acids, methacrylic acids, maleic acids and mixed polymers of these, which can also contain small proportions of polymerizable substances without carb
  • the relative molecular mass of the homopolymers of unsaturated carboxylic acids is generally between 3,000 and 200,000, and that of the copolymers between 2,000 and 200,000, preferably 30,000 to 120,000, in each case based on the free acid.
  • a particularly preferred acrylic acid-maleic acid copolymer has a molecular weight of 30,000 to 100,000.
  • Commercially available products are, for example, Sokalan® CP 5, CP 10 and PA 30 from BASF.
  • Suitable, although less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinyl methyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of the acid is at least 50% by weight.
  • Terpolymers which contain two unsaturated acids and/or their salts as monomers and vinyl alcohol and/or an esterified vinyl alcohol or a carbohydrate as the third monomer can also be used as water-soluble organic builder substances.
  • the first acidic monomer or its salt is derived from a monoethylenically unsaturated C 3 -C 8 -carboxylic acid and preferably from a C 3 -C 4 -monocarboxylic acid, in particular from (meth)acrylic acid.
  • the second acidic monomer or its salt can be a derivative of a C 4 -C 8 -dicarboxylic acid, maleic acid being particularly preferred, and/or a derivative of an allylsulfonic acid which is substituted in the 2-position with an alkyl or aryl radical.
  • Such polymers generally have a molecular weight between 1,000 and 200,000.
  • Further preferred copolymers are those which preferably have acrolein and acrylic acid/acrylic acid salts or vinyl acetate as monomers.
  • the organic builder substances can be used in the form of aqueous solutions, preferably in the form of 30 to 50 percent by weight aqueous solutions, particularly for the production of liquid agents. All of the acids mentioned are generally used in the form of their water-soluble salts, in particular their alkali metal salts.
  • Such organic builder substances can, if desired, be present in amounts of up to 40% by weight, in particular up to 25% by weight and preferably from 1% by weight to 8% by weight. Amounts close to the upper limit mentioned are preferably used in pasty or liquid, in particular aqueous, compositions.
  • Suitable water-soluble inorganic builder materials are, in particular, alkali metal silicates, alkali metal carbonates and alkali metal phosphates, which can be present in the form of their alkaline, neutral or acidic sodium or potassium salts.
  • alkali metal silicates alkali metal carbonates and alkali metal phosphates, which can be present in the form of their alkaline, neutral or acidic sodium or potassium salts.
  • alkali metal silicates alkali metal carbonates and alkali metal phosphates
  • alkali metal phosphates which can be present in the form of their alkaline, neutral or acidic sodium or potassium salts.
  • examples of these are trisodium phosphate, tetrasodium diphosphate, disodium dihydrogen diphosphate, pentasodium triphosphate, so-called sodium hexametaphosphate, oligomeric trisodium phosphate with degrees of oligomerization from 5 to 1000, in particular 5 to
  • crystalline or amorphous alkali metal aluminosilicates in amounts of up to 50% by weight, preferably not more than 40% by weight and in liquid compositions, in particular from 1% by weight to 5% by weight, are used as water-insoluble, water-dispersible inorganic builder materials. deployed.
  • the crystalline sodium aluminosilicates of detergent quality in particular zeolites A, P and optionally X, alone or in mixtures, for example in the form of a co-crystallizate of zeolites A and X ( Vegobond® AX, a commercial product from Condea Augusta SpA), are preferred .
  • Amounts close to the upper limit mentioned are preferably used in solid, particulate compositions.
  • suitable aluminosilicates do not have any particles with a particle size of more than 30 ⁇ m and preferably consist of at least 80% by weight of particles with a size of less than 10 ⁇ m.
  • Your calcium binding capacity, for example, according to the German patent DE2412837 can be determined is usually in the range of 100 to 200 mg CaO per gram.
  • Suitable substitutes or partial substitutes for the aluminosilicate mentioned are crystalline alkali metal silicates, which can be present alone or in a mixture with amorphous silicates.
  • the alkali metal silicates which can be used as builders in the agents preferably have a molar ratio of alkali metal oxide to SiO 2 below 0.95, in particular from 1:1.1 to 1:12, and can be present in amorphous or crystalline form.
  • Preferred alkali silicates are the sodium silicates, in particular the amorphous sodium silicates, with a molar Na 2 O:SiO 2 ratio of 1:2 to 1:2.8.
  • Crystalline phyllosilicates of the general formula Na 2 Si x O 2x+1 y H 2 O are preferably used as crystalline silicates, which can be present alone or in a mixture with amorphous silicates, in which x, the so-called modulus, is a number from 1, 9 to 22, in particular 1.9 to 4 and y is a number from 0 to 33 and preferred values for x are 2, 3 or 4.
  • Preferred crystalline layered silicates are those in which x has the value 2 or 3 in the general formula mentioned. In particular, both ⁇ - and ⁇ -sodium dinitrates (Na 2 Si 2 O 5 .yH 2 O) are preferred.
  • Crystalline layered silicates of the above formula (I) are marketed by Clariant GmbH under the trade name Na-SKS, for example Na-SKS-1 (Na 2 Si 22 O 45 .xH 2 O, kenyaite), Na-SKS -2 (Na 2 Si 14 O 29 xH 2 O, magadiite), Na-SKS-3 (Na 2 Si 8 O 17 xH 2 O) or Na-SKS-4 (Na 2 Si 4 O 9 xH 2 O, makatite).
  • Na-SKS for example Na-SKS-1 (Na 2 Si 22 O 45 .xH 2 O, kenyaite), Na-SKS -2 (Na 2 Si 14 O 29 xH 2 O, magadiite), Na-SKS-3 (Na 2 Si 8 O 17 xH 2 O) or Na-SKS-4 (Na 2 Si 4 O 9 xH 2 O, makatite).
  • Na-SKS-5 ⁇ -Na 2 Si 2 O 5
  • Na-SKS-7 ß-Na 2 Si 2 O 5 , Natrosilit
  • Na-SKS-9 NaHSi 2 O 5
  • Na-SKS-10 NaHSi 2 O 5 3H 2 O, kanemite
  • Na-SKS-11 t-Na 2 Si 2 O 5
  • Na-SKS-13 NaHSi 2 O 5
  • Na-SKS-6 ⁇ -Na 2 Si 2 O 5
  • a granular compound of crystalline layered silicate and citrate, of crystalline layered silicate and the abovementioned (co)polymeric polycarboxylic acid, or of alkali metal silicate and alkali metal carbonate is used, as is the case, for example, under the name Nabion® 15 is commercially available.
  • Builder substances are preferably present in the compositions in amounts of up to 75% by weight, in particular 5% by weight to 50%.
  • the organic solvents that can be used in addition to water in the detergents or cleaning agents according to the invention, especially if they are in liquid or pasty form, include alcohols with 1 to 4 carbon atoms, in particular methanol, ethanol, isopropanol and tert-butanol, diols with 2 up to 4 carbon atoms, in particular ethylene glycol and propylene glycol, and mixtures thereof and the ethers which can be derived from the classes of compounds mentioned.
  • Such water-miscible solvents are preferably present in the compositions in amounts of not more than 30% by weight, in particular from 6% by weight to 20% by weight.
  • the organic solvents used are particularly preferably miscible with water.
  • the washing or cleaning agent according to the invention can contain enzymes, for example, without being limited thereto, amylases, proteases, cellulases, glycosidases, hemicellulases, mannanases, xylanases, pecinases, ⁇ -glucosidases, carrageenases, lipases, oxidases, oxidoreductases or combinations thereof.
  • Amylases and/or proteases are preferably used.
  • the compositions may contain enzyme stabilizers or inhibitors.
  • the composition according to the invention or the agent according to the invention is phosphate-free and/or phosphonate-free.
  • “Phosphate-free” and “phosphonate-free” as used herein means that the composition in question is essentially free of phosphates or phosphonates, i.e. in particular phosphates or phosphonates in amounts less than 0.1% by weight, preferably less than 0 .01% by weight, based on the respective composition or the respective agent.
  • the pH of the compositions or agents can be adjusted using customary pH regulators.
  • Acids and/or alkalis preferably alkalis, are used as pH adjusters.
  • Suitable acids are, in particular, organic acids such as acetic acid, citric acid, glycolic acid, lactic acid, succinic acid, adipic acid, malic acid, tartaric acid and gluconic acid or amidosulfonic acid.
  • the mineral acids hydrochloric acid, sulfuric acid and nitric acid or mixtures thereof can also be used.
  • Suitable bases come from the group of alkali metal and alkaline earth metal hydroxides and carbonates, in particular the alkali metal hydroxides, of which potassium hydroxide is preferred.
  • the alkali source described above is particularly preferably used to adjust the pH. Even if volatile alkali, for example in the form of ammonia and/or alkanolamines, which can contain up to 9 carbon atoms in the molecule, can be used to adjust the pH, the alkanolamine here being able to be selected from the group consisting of mono -, Di-, triethanol- and -propanolamine and mixtures thereof, such volatile alkali sources, in particular ethanolamines, are preferably avoided.
  • the compositions therefore contain less than 1.75% by weight of alkanolamine, in particular monoethanolamine, and are very particularly preferably free of it. It was found that the omission of such alkanolamines increases the stability of the compositions or compositions.
  • the composition according to the invention or the agent according to the invention can contain one or more buffer substances (INCI buffering agents), usually in amounts of 0.001 to 5% by weight.
  • buffer substances which are at the same time complexing agents or even chelating agents (chelators, INCI chelating agents) are preferred.
  • Particularly preferred buffer substances are citric acid or citrates, in particular sodium and potassium citrates, for example trisodium citrate ⁇ 2H 2 O and tripotassium citrate H 2 O.
  • the preparation of the agents described herein can take place in different ways.
  • the liquid supply forms based on water and/or organic solvents can be thickened and in the form of gels.
  • the agent or the respective liquid composition has a viscosity above 200 mPas (Brookfield Viscometer DV-II+Pro, spindle 25, 30 rpm, 20° C.), in particular between 400 and 6000 mPas, directly after production.
  • the detergents and cleaning agents described herein are preferably prepackaged to form dosing units. These dosing units preferably comprise the amount of washing or cleaning active substances required for one cleaning cycle. Preferred dosage units weigh between 12 and 30 g. The volume of the aforementioned dosing units and their three-dimensional shape are particularly preferably selected in such a way that the prefabricated units can be dosed via the dosing chamber of a washing machine or dishwasher. The volume of the dosage unit is therefore preferably between 10 and 35 ml, preferably between 12 and 30 ml.
  • the water-soluble cover is preferably formed from a water-soluble film material which is selected from the group consisting of polymers or polymer mixtures.
  • the cover can be formed from one or from two or more layers of the water-soluble film material.
  • the water-soluble film material of the first layer and the further layers, if any, can be the same or different. Films are particularly preferred which can be glued and/or sealed to form packaging such as tubes or pillows after they have been filled with an agent.
  • the foils are in the form of multi-chamber pouches in which different compositions or components can be spatially separated.
  • the water-soluble shell contains polyvinyl alcohol or a polyvinyl alcohol copolymer.
  • Water-soluble coatings that contain polyvinyl alcohol or a polyvinyl alcohol copolymer have good stability with sufficiently high water solubility, especially cold water solubility.
  • Suitable water-soluble films for producing the water-soluble covering are preferably based on a polyvinyl alcohol or a polyvinyl alcohol copolymer whose molecular weight is in the range from 10,000 to 1,000,000 gmol -1 , preferably from 20,000 to 500,000 gmol -1 , particularly preferably from 30,000 to 100,000 gmol -1 and in particular from 40,000 to 80,000 gmol -1 .
  • Polyvinyl alcohol is usually produced by hydrolysis of polyvinyl acetate, since the direct synthesis route is not possible. The same applies to polyvinyl alcohol copolymers, which are correspondingly produced from polyvinyl acetate copolymers. It is preferred if at least one layer of the water-soluble coating comprises a polyvinyl alcohol whose degree of hydrolysis is 70 to 100 mol %, preferably 80 to 90 mol %, particularly preferably 81 to 89 mol % and in particular 82 to 88 mol %.
  • a polyvinyl alcohol-containing film material suitable for producing the water-soluble casing can also have a polymer selected from the group consisting of (meth)acrylic acid-containing (co)polymers, polyacrylamides, oxazoline polymers, polystyrene sulfonates, polyurethanes, polyesters, polyethers, polylactic acid or mixtures of the above Polymers can be added.
  • a preferred additional polymer are polylactic acids.
  • preferred polyvinyl alcohol copolymers include dicarboxylic acids as further monomers. Suitable dicarboxylic acids are itaconic acid, malonic acid, succinic acid and mixtures thereof, with itaconic acid being preferred.
  • Polyvinyl alcohol copolymers which are also preferred include, in addition to vinyl alcohol, an ethylenically unsaturated carboxylic acid, its salt or its ester.
  • Such polyvinyl alcohol copolymers particularly preferably contain, in addition to vinyl alcohol, acrylic acid, methacrylic acid, acrylic acid esters, methacrylic acid esters or mixtures thereof.
  • the film material contains further additives.
  • the film material can contain, for example, plasticizers such as dipropylene glycol, ethylene glycol, diethylene glycol, propylene glycol, glycerol, sorbitol, mannitol or mixtures thereof.
  • Further additives include, for example, release aids, fillers, crosslinking agents, surfactants, antioxidants, UV absorbers, anti-blocking agents, anti-adhesive agents or mixtures thereof.
  • Suitable water-soluble films for use in the water-soluble wrappers of the water-soluble packages according to the invention are films sold by MonoSol LLC, for example under the designation M8630, C8400 or M8900.
  • Other suitable films include Solublon® PT, Solublon® GA, Solublon® KC or Solublon® KL films from Aicello Chemical Europe GmbH or Kuraray VF-HP films.
  • the surface to be cleaned is particularly preferably a fabric, crockery, a piece of furniture, a (floor) or (wall) tiles, in particular a hard surface such as crockery, a piece of furniture, a (floor) or (wall) tiles .
  • the invention preferably relates to the use of the perfume composition according to the invention or the washing or cleaning agent according to the invention for washing textiles or for cleaning surfaces and at the same time for scenting the room in which the composition or the agent is used.
  • a room-filling perfume effect is brought about by the use of the perfume composition according to the invention or the washing or cleaning agent according to the invention.
  • This effect preferably occurs in addition to the cleaning (laundry) of textiles or the cleaning of other surfaces, preferably hard surfaces.
  • the space-filling effect occurs both during use, for example when wiping a floor or while washing textiles, for example when washing by hand, and afterwards, for example when the washing machine is opened or the laundry is drying on the line. It is particularly preferred that the room-filling perfume effect lasts in the room for a period of time.
  • At least 30 seconds from the end of application more preferably at least 1 minute, even more preferably at least 2 minutes, even more preferably at least 5 minutes, even more preferably at least 10 minutes more preferably at least 15 minutes, even more preferably at least 30 minutes, even more preferably at least 60 minutes, or especially at least 120 minutes or longer from the end of application.
  • the invention preferably relates to a method for washing textiles or cleaning surfaces and at the same time for scenting the room in which the method is carried out, characterized in that a perfume composition according to the invention or a detergent or cleaning agent according to the invention is used in at least one method step.
  • the surface to be cleaned is particularly preferably a fabric, crockery, a piece of furniture, a (floor) or (wall) tiles, in particular a hard surface such as crockery, a piece of furniture, a (floor) or (wall) tiles .
  • the method according to the invention comprises, for example, washing textiles in an automatic washing machine or cleaning dishes in a dishwasher, the agent according to the invention or the composition according to the invention during the running through of a washing or dishwashing program before the start of the main wash cycle or in the course of the main wash cycle in the interior a washing machine or dishwasher.
  • the agent according to the invention can be dosed or introduced into the interior of the washing machine or dishwasher manually; alternatively, the agent can be dosed into the interior of the washing machine or dishwasher by means of the dosing chamber.
  • the method according to the invention also includes manual processes, with mechanical processes being preferred.
  • Manual methods can be, for example, the cleaning, eg cleaning or mopping, of floor surfaces or wall tiles.
  • the manual washing of textiles is also included.
  • the methods according to the invention are characterized in particular by the fact that the composition according to the invention or the washing or cleaning agent according to the invention is brought into contact with the items to be cleaned in one or more method steps.
  • the composition or agent can be used undiluted or diluted, for example, with water or another suitable solvent.
  • the items to be cleaned can be treated simultaneously or successively with other components, compositions or agents.
  • the relevant fragrance molecules are preferably released and, because of their properties, can bring about the desired room-filling perfume effect, which particularly preferably persists in the room for some time, as defined above.
EP22160242.8A 2022-03-04 2022-03-04 Coefficient d'efflorescence Pending EP4239049A1 (fr)

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EP22160242.8A EP4239049A1 (fr) 2022-03-04 2022-03-04 Coefficient d'efflorescence
PCT/EP2023/054771 WO2023165910A1 (fr) 2022-03-04 2023-02-27 Coefficient d'efflorescence

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EP22160242.8A EP4239049A1 (fr) 2022-03-04 2022-03-04 Coefficient d'efflorescence

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Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2412837A1 (de) 1973-04-13 1974-10-31 Henkel & Cie Gmbh Verfahren zum waschen und reinigen der oberflaechen von festen werkstoffen, insbesondere von textilien, sowie mittel zur durchfuehrung des verfahrens
US4476041A (en) * 1982-06-04 1984-10-09 International Flavors & Fragrances Inc. Process for augmenting or enhancing the fresh air aroma of consumable materials with a mixture of n-alkanals having from 6 to 15 carbon atoms
EP1285906A2 (fr) * 2001-08-20 2003-02-26 Haarmann & Reimer Gmbh Compositions à libération contrôlée d'un aldéhyde ou cétone, d'un alcool et d'un acide carboxylique
US20070099804A1 (en) * 2005-04-07 2007-05-03 Addi Fadel Perfumes for rinse-off systems
WO2009121725A1 (fr) 2008-04-02 2009-10-08 Henkel Ag & Co. Kgaa Agents de lavage et de nettoyage contenant des protéases sécrétées par xanthomonas
WO2012084292A1 (fr) * 2010-12-21 2012-06-28 Henkel Ag & Co. Kgaa Composition de parfum comprenant un composant odorant aldéhyde ou -cétone et précurseur de composant odorant oxazolidine
DE102015217876A1 (de) * 2015-09-17 2017-03-23 Henkel Ag & Co. Kgaa Parfümzusammensetzung mit Geruchsmodulatorverbindungen und Kieselsäureestern zur Steigerung und Verlängerung der Duftintensität
EP3257927A1 (fr) * 2016-06-15 2017-12-20 The Procter & Gamble Company Composition détergente liquide pour le lavage
EP3900696A1 (fr) * 2020-04-21 2021-10-27 Takasago International Corporation Composition de parfum encapsulée

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2412837A1 (de) 1973-04-13 1974-10-31 Henkel & Cie Gmbh Verfahren zum waschen und reinigen der oberflaechen von festen werkstoffen, insbesondere von textilien, sowie mittel zur durchfuehrung des verfahrens
US4476041A (en) * 1982-06-04 1984-10-09 International Flavors & Fragrances Inc. Process for augmenting or enhancing the fresh air aroma of consumable materials with a mixture of n-alkanals having from 6 to 15 carbon atoms
EP1285906A2 (fr) * 2001-08-20 2003-02-26 Haarmann & Reimer Gmbh Compositions à libération contrôlée d'un aldéhyde ou cétone, d'un alcool et d'un acide carboxylique
US20070099804A1 (en) * 2005-04-07 2007-05-03 Addi Fadel Perfumes for rinse-off systems
WO2009121725A1 (fr) 2008-04-02 2009-10-08 Henkel Ag & Co. Kgaa Agents de lavage et de nettoyage contenant des protéases sécrétées par xanthomonas
WO2012084292A1 (fr) * 2010-12-21 2012-06-28 Henkel Ag & Co. Kgaa Composition de parfum comprenant un composant odorant aldéhyde ou -cétone et précurseur de composant odorant oxazolidine
DE102015217876A1 (de) * 2015-09-17 2017-03-23 Henkel Ag & Co. Kgaa Parfümzusammensetzung mit Geruchsmodulatorverbindungen und Kieselsäureestern zur Steigerung und Verlängerung der Duftintensität
EP3257927A1 (fr) * 2016-06-15 2017-12-20 The Procter & Gamble Company Composition détergente liquide pour le lavage
EP3900696A1 (fr) * 2020-04-21 2021-10-27 Takasago International Corporation Composition de parfum encapsulée

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
RODRIGUES ALÍRIO E. ET AL: "Perfume and Flavor Engineering: A Chemical Engineering Perspective", MOLECULES, vol. 26, no. 11, 22 June 2021 (2021-06-22), DE, pages 3095, XP055922926, ISSN: 1433-1373, DOI: 10.3390/molecules26113095 *

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