EP1994133B1 - Lessive protégeant les couleurs - Google Patents

Lessive protégeant les couleurs Download PDF

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Publication number
EP1994133B1
EP1994133B1 EP07703336A EP07703336A EP1994133B1 EP 1994133 B1 EP1994133 B1 EP 1994133B1 EP 07703336 A EP07703336 A EP 07703336A EP 07703336 A EP07703336 A EP 07703336A EP 1994133 B1 EP1994133 B1 EP 1994133B1
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stands
acid
hal
textiles
group
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German (de)
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EP1994133A1 (fr
Inventor
Josef Penninger
Birgit GLÜSEN
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Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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Priority to PL07703336T priority Critical patent/PL1994133T3/pl
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/26—Organic compounds containing nitrogen
    • C11D3/28—Heterocyclic compounds containing nitrogen in the ring
    • 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
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0021—Dye-stain or dye-transfer inhibiting compositions

Definitions

  • the present invention relates to the use of carboxylated triazine derivatives as dye transfer inhibiting agents in the washing of textiles and detergents containing such compounds.
  • Detergents contain in addition to the indispensable for the washing process ingredients such as surfactants and builders usually other ingredients that can be summarized under the term washing aids and the so different drug groups such as foam regulators, graying inhibitors, bleach, bleach activators and enzymes include.
  • auxiliaries also include substances which are intended to prevent dyed textiles from causing a changed color impression after washing. This color impression change washed, i. cleaner, textiles can be based on the one hand on the fact that dye components are removed by the washing process from the textile ("fading"), on the other hand may be deposited by differently colored textiles dyes on the textile ("discoloration").
  • the discoloration aspect may also play a role in undyed laundry items when washed together with colored laundry items.
  • detergents In order to avoid these undesirable side effects of removing dirt from textiles by treatment with usually surfactant-containing aqueous systems, detergents, especially when they are provided as so-called color or colored laundry detergents for colored textiles, contain active ingredients which prevent the detachment of dyes from the textile or At least the deposition of detached, located in the wash liquor to avoid dyes on textiles.
  • Many of the commonly used polymers have such a high affinity for dyes that they draw them more from the dyed fiber, resulting in increased color losses.
  • Another object of the invention is a color-protective detergent, comprising a color transfer inhibitor in the form of a Triaziriderivates the above-defined general formula II in addition to conventional ingredients compatible with this ingredient.
  • Triazine derivatives of general formula I are obtainable by reacting 2,4,6-trihalo-1,3,5-triazines with 1 or 2 equivalents of aminoaryl compound, wherein the aryl group of the aminoaryl compound carries at least 1 carboxy substituent. It is preferably a 1 to 3-fold carboxylic acid or carboxylate-substituted benzene unit.
  • Suitable aminoaryl compounds are, for example, 2-aminobenzoic acid, 3-aminobenzoic acid, 4-aminobenzoic acid, 3-amino-1,2-benzenedicarboxylic acid, 4-amino-1,2-benzenedicarboxylic acid, 2-amino-1,3-benzenedicarboxylic acid, 4-amino-1,3- benzene dicarboxylic acid, 5-amino-1,3-benzenedicarboxylic acid, 2-amino-1,4-benzenedicarboxylic acid, 4-amino-1,2,3-benzenetricarboxylic acid, 3-amino-1,2,4-benzenetricarboxylic acid, 5-amino 1,2,4-benzenetricarboxylic acid, 6-amino-1,2,4-benzenetricarboxylic acid and 2-amino-1,3,5-benzenetricarboxylic acid, wherein their carboxylic acid groups may also be in salt form. It is also possible to
  • Preferred oligo- or polyethylenimines are those of the formula NH 2 -CH 2 CH 2 - (NH-CH 2 CH 2 -) n NH 2 , in which n is a number from 1 to 30, in particular 2 to 20, whereby also Mixtures of oligo- or polyethyleneimines of different degrees of oligo- or polymerization can be used so that n can take as an average value and non-integer values.
  • An agent according to the invention preferably contains from 0.05% by weight to 2% by weight, in particular from 0.2% by weight to 1% by weight, of dye-transfer-inhibiting compound of the general formula II.
  • the compounds of the general formula I or II contribute to both aspects of the color constancy mentioned above, ie they reduce it both discoloration and fading, although the effect of preventing staining, especially when washing white textiles, is most pronounced.
  • Another object of the invention is therefore the use of a corresponding compound to prevent the change in the color impression of textiles in their washing in particular surfactant-containing aqueous solutions. Under the change in the color impression is by no means the difference between dirty and clean textile to understand, but the difference between each clean textile before and after the washing process.
  • Another object of the invention is a process for washing dyed textiles in surfactant-containing aqueous solutions, which is characterized in that one uses a surfactant-containing aqueous solution containing a compound of general formula II. In such a process, it is possible to wash white or undyed textiles together with the dyed textile without the white or undyed textile being dyed.
  • An agent according to the invention may, in addition to the compound of the formula II, if desired, comprise a known dye transfer inhibitor, then preferably in amounts of from 0.1% by weight to 2% by weight, in particular from 0.2% by weight to 1% by weight, which, in a preferred embodiment of the invention, is a polymer of vinylpyrrolidone, vinylimidazole, vinylpyridine-N-oxide or a copolymer thereof.
  • a mediator compound for the peroxidase for example one from the international patent application WO 96/10079 known acetosyringone, one from the international patent application WO 96/12845 known phenol derivative or one from the international patent application WO 96/12846 known phenotiazine or phenoxazine, is preferred in this case, whereby also above-mentioned polymeric Farbübertragungsinhibitorwirkstoffe can be used.
  • Polyvinylpyrrolidone preferably has an average molecular weight in the range from 10 000 to 60 000, in particular in the range from 25 000 to 50 000, for use in compositions according to the invention.
  • those of vinylpyrrolidone and vinylimidazole in a molar ratio of 5: 1 to 1: 1 having an average molecular weight in the range of 5,000 to 50,000, especially 10,000 to 20,000 are preferred.
  • the detergents according to the invention may in principle contain, in addition to the active ingredient used in accordance with the invention, all known ingredients customary in such agents.
  • the agents according to the invention may in particular be builders, surface-active surfactants, bleaches based on organic and / or inorganic peroxygen compounds, bleach activators, water-miscible organic solvents, enzymes, sequestering agents, electrolytes, pH regulators and other auxiliaries, such as optical brighteners, grayness inhibitors, foam regulators and colorants Contain fragrances.
  • compositions according to the invention may comprise one or more surfactants, in particular anionic surfactants, nonionic surfactants and mixtures thereof, but also cationic, zwitterionic and amphoteric surfactants.
  • Suitable nonionic surfactants are in particular alkyl glycosides and ethoxylation and / or propoxylation of alkyl glycosides or linear or branched alcohols each having 12 to 18 carbon atoms in the alkyl moiety and 3 to 20, preferably 4 to 10 alkyl ether groups. Also suitable are ethoxylation and / or propoxylation products of N-alkylamines, vicinal diols, fatty acid esters and fatty acid amides which correspond to said long-chain alcohol derivatives with respect to the alkyl moiety and of alkylphenols having 5 to 12 carbon atoms in the alkyl radical.
  • the nonionic surfactants used are preferably alkoxylated, advantageously ethoxylated, in particular primary, alcohols having preferably 8 to 18 carbon atoms and on average 1 to 12 moles of ethylene oxide (EO) per mole of alcohol in which the alcohol residue is linear or preferably methyl-branched in the 2-position may be or contain linear and methyl-branched radicals in the mixture, as they are usually present in Oxoalkoholresten.
  • EO ethylene oxide
  • alcohol ethoxylates with linear radicals of alcohols of natural origin having 12 to 18 carbon atoms, for example of coconut, palm, tallow or oleyl alcohol, and on average 2 to 8 EO per mole of alcohol are preferred.
  • the preferred ethoxylated alcohols include, for example, C 12 -C 14 -alcohols with 3 EO or 4 EO, C 9 -C 11 -alcohols with 7 EO, C 13 -C 15 -alcohols with 3 EO, 5 EO, 7 EO or 8 EO, C 12 -C 18 -alcohols with 3 EO, 5 EO or 7 EO and mixtures of these, such as mixtures of C 12 -C 14 -alcohol with 3 EO and C 12 -C 18 -alcohol with 7 EO.
  • the degrees of ethoxylation given represent statistical means which, for a particular product, may be an integer or a fractional number.
  • Preferred alcohol ethoxylates have a narrow homolog distribution (narrow range ethoxylates, NRE).
  • fatty alcohols with more than 12 EO can also be used. Examples include (tallow) fatty alcohols with 14 EO, 16 EO, 20 EO, 25 EO, 30 EO or 40 EO.
  • agents for use in mechanical processes usually extremely low-foam compounds are used. These include preferably C 12 -C 18 -alkylpolyethylenglykol-polypropylene glycol ethers with in each case at to 8 mol ethylene oxide and propylene oxide units in the molecule.
  • the nonionic surfactants also include alkyl glycosides of the general formula RO (G) x in which R is a primary straight-chain or methyl-branched, in particular 2-methyl-branched aliphatic radical having 8 to 22, preferably 12 to 18 carbon atoms and G represents a glycose unit having 5 or 6 C atoms, preferably glucose.
  • the degree of oligomerization x which indicates the distribution of monoglycosides and oligoglycosides, is an arbitrary number - which, as a variable to be determined analytically, may also assume fractional values - between 1 and 10; preferably x is 1.2 to 1.4.
  • polyhydroxy fatty acid amides of the formula (II) in which R 1 is CO for an aliphatic acyl radical having 6 to 22 carbon atoms, R 2 is hydrogen, an alkyl or hydroxyalkyl radical having 1 to 4 carbon atoms and [Z] is a linear or branched polyhydroxyalkyl radical having 3 to 10 carbon atoms and 3 to 10 hydroxyl groups:
  • the polyhydroxy fatty acid amides are preferably derived from reducing sugars having 5 or 6 carbon atoms, in particular from glucose.
  • the group of polyhydroxy fatty acid amides also includes compounds of the formula (IV) in the R 3 is a linear or branched alkyl or alkenyl radical having 7 to 12 carbon atoms, R 4 is a linear, branched or cyclic alkylene radical or a Arylene radical having 2 to 8 carbon atoms and R 5 is a linear, branched or cyclic alkyl radical or an aryl radical or an oxy-alkyl radical having 1 to 8 carbon atoms, wherein C 1 -C 4 alkyl or phenyl radicals are preferred, and [Z] is a linear polyhydroxyalkyl radical whose alkyl chain is substituted by at least two hydroxyl groups, or alkoxylated, preferably ethoxylated or propoxylated derivatives of this radical.
  • [Z] is also obtained here preferably by reductive amination of a sugar such as glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • a sugar such as glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • the N-alkoxy- or N-aryloxy-substituted compounds can then be used, for example, according to the teaching of the international patent application WO 95/07331 be converted by conversion with fatty acid methyl esters in the presence of an alkoxide as catalyst into the desired Polyhydroxyfettklaamide.
  • nonionic surfactants used either as the sole nonionic surfactant or in combination with other nonionic surfactants, in particular together with alkoxylated fatty alcohols and / or alkyl glycosides, are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters, preferably from 1 to 4 carbon atoms in the alkyl chain, in particular fatty acid methyl ester, as described for example in the Japanese patent application JP 58/217598 are described or preferably according to the in the international patent application WO 90/13533 be prepared described methods.
  • Nonionic surfactants of the amine oxide type for example N-cocoalkyl-N, N-dimethylamine oxide and N-tallowalkyl-N, N-dihydroxyethylamine oxide, and the fatty acid alkanolamides may also be suitable.
  • the amount of these nonionic surfactants is preferably not more than that of the ethoxylated fatty alcohols, especially not more than half thereof.
  • Other suitable surfactants are so-called gemini surfactants. These are generally understood as meaning those compounds which have two hydrophilic groups per molecule. These groups are usually separated by a so-called "spacer". This spacer is usually a carbon chain that should be long enough for the hydrophilic groups to be spaced sufficiently apart for them to act independently of each other.
  • Such surfactants are generally characterized by an unusually low critical micelle concentration and the ability to greatly reduce the surface tension of the water.
  • Gemini surfactants not only such "dimeric", but also understood according to “trimeric” surfactants.
  • Suitable gemini surfactants are, for example, sulfated hydroxy mixed ethers according to the German patent application DE 43 21 022 or dimer alcohol bis and trimer alcohol tris sulfates and ether sulfates according to the German patent application DE 195 03 061 , End-capped dimeric and trimeric mixed ethers according to the German patent application DE 195 13 391 They are characterized by their bi- and multi-functionality.
  • end-capped surfactants mentioned have good wetting properties and are low foaming, so that they are particularly suitable for use in machine washing or cleaning processes.
  • gemini-polyhydroxy fatty acid amides or poly-polyhydroxy fatty acid amides as described in international patent applications WO 95/19953 .
  • WO 95/19954 and the US patents US 3,234,258 or US 5 075 041 which can be obtained as commercial products of the Shell Oil Company under the name DAN® are suitable anionic surfactants.
  • sulfuric acid monoesters of straight-chain or branched C 7 -C 21 -alcohols ethoxylated with from 1 to 6 mol of ethylene oxide such as 2-methyl-branched C 9 -C 11 -alcohols having on average 3.5 mol of ethylene oxide (EO) or C 12 - C 18 -fatty alcohols with 1 to 4 EO.
  • EO ethylene oxide
  • the preferred anionic surfactants also include the salts of alkylsulfosuccinic acid, which are also referred to as sulfosuccinates or as sulfosuccinic acid esters, and the monoesters and / or diesters of sulfosuccinic acid with alcohols, preferably fatty alcohols and in particular ethoxylated fatty alcohols.
  • alcohols preferably fatty alcohols and in particular ethoxylated fatty alcohols.
  • Preferred sulfosuccinates contain C 8 to C 18 fatty alcohol residues or mixtures of these.
  • Particularly preferred sulfosuccinates contain a fatty alcohol residue derived from ethoxylated fatty alcohols, which by themselves are nonionic surfactants.
  • Sulfosuccinates whose fatty alcohol residues are derived from ethoxylated fatty alcohols with a narrow homolog distribution, are again particularly preferred.
  • alk (en) ylsuccinic acid having preferably 8 to 18 carbon atoms in the alk (en) yl chain or salts thereof.
  • Suitable further anionic surfactants are fatty acid derivatives of amino acids, for example N-methyltaurine (Tauride) and / or N-methylglycine (sarcosides).
  • sarcosides or the sarcosinates and here especially sarcosinates of higher and possibly simple or polyunsaturated fatty acids such as oleyl sarcosinate.
  • anionic surfactants are particularly soaps into consideration.
  • Particularly suitable are saturated fatty acid soaps, such as the salts of lauric acid, myristic acid, palmitic acid, stearic acid, hydrogenated erucic acid and behenic acid and, in particular, soap mixtures derived from natural fatty acids, for example coconut, palm kernel or tallow fatty acids. Together with these soaps or as a substitute for soaps, it is also possible to use the known alkenylsuccinic acid salts.
  • the anionic surfactants may be in the form of their sodium, potassium or ammonium salts and as soluble salts of organic bases, such as mono-, di- or triethanolamine.
  • the anionic surfactants are preferably present in the form of their sodium or potassium salts, in particular in the form of the sodium salts.
  • Surfactants are present in detergents according to the invention in proportions of preferably from 5% by weight to 50% by weight, in particular from 8% by weight to 30% by weight.
  • An agent according to the invention preferably contains at least one water-soluble and / or water-insoluble, organic and / or inorganic builder.
  • the water-soluble organic builder substances include polycarboxylic acids, in particular citric acid and sugar-seeds, monomeric and polymeric aminopolycarboxylic acids, in particular methylglycinediacetic acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid and polyaspartic acid, polyphosphonic acids, in particular 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 accessible by oxidation of polysaccharides or dextrins polycarboxylates of the European patent specification EP 0 625 992 or the international patent application WO 92/18542 or the European patent specification EP 0
  • the molecular weight of the homopolymers of unsaturated carboxylic acids is generally between 3,000 and 200,000, of the copolymers between 2,000 and 200,000, preferably 30,000 to 120,000, each 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, though 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 acid is at least 50% by weight.
  • 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 may be a derivative of a C 4 -C 8 -dicarboxylic acid, with maleic acid being particularly preferred, and / or a derivative of an allylsulfonic acid which is substituted in the 2-position by an alkyl or aryl radical.
  • Such polymers can be prepared in particular by methods described in the German patent DE 42 21 381 and the German patent application DE 43 00 772 are generally described, and generally have a molecular weight between 1,000 and 200,000. Further preferred copolymers are those described in the German patent applications DE 43 03 320 and DE 44 17 734 be described and as monomers preferably acrolein and acrylic acid / acrylic acid salts or vinyl acetate.
  • the organic builder substances can be used, in particular for the preparation of liquid agents, in the form of aqueous solutions, preferably in the form of 30 to 50 percent by weight aqueous solutions. All of the acids mentioned are generally used in the form of their water-soluble salts, in particular their alkali metal salts.
  • organic builder substances may 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. Quantities close to the stated upper limit are preferably used in paste-form or liquid, in particular water-containing, agents according to the invention.
  • water-soluble inorganic builder materials are in particular alkali metal silicates, alkali metal carbonates and alkali metal phosphates, in the form of their alkaline, neutral or acidic Sodium or potassium salts may be present, into consideration.
  • alkali metal silicates alkali metal carbonates and alkali metal phosphates
  • neutral or acidic Sodium or potassium salts may be present, into consideration.
  • examples of these are trisodium phosphate, tetrasodium diphosphate, disodium dihydrogen diphosphate, pentasodium triphosphate, so-called sodium hexametaphosphate, oligomeric trisodium phosphate with degrees of oligomerization of 5 to 1000, in particular 5 to 50, and the corresponding potassium salts or mixtures of sodium and potassium salts.
  • Crystalline or amorphous alkali metal aluminosilicates in amounts of up to 50% by weight, preferably not more than 40% by weight, and in liquid agents, in particular from 1% by weight to 5% by weight, are particularly suitable as water-insoluble, water-dispersible inorganic builder materials.
  • suitable aluminosilicates have no particles with a particle size greater than 30 .mu.m and preferably consist of at least 80% by weight of particles having a size of less than 10 .mu.m.
  • Their calcium binding capacity is usually in the range of 100 to 200 mg CaO per gram.
  • Suitable substitutes or partial substitutes for the said aluminosilicate are crystalline alkali silicates which may be present alone or in a mixture with amorphous silicates.
  • the alkali metal silicates useful as builders in the compositions according to the invention 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 may be present in amorphous or crystalline form.
  • Preferred alkali metal silicates are the sodium silicates, in particular the amorphous sodium silicates, with a molar ratio of Na 2 O: SiO 2 of 1: 2 to 1: 2.8.
  • crystalline silicates which may be present alone or in admixture with amorphous silicates, are crystalline layer silicates with the general formula Na 2 Si x O y are used 2x + 1 H 2 O, in which x, the so-called module, 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. Crystalline phyllosilicates, which fall under this general formula, for example, in the European patent application EP 0 164 514 described.
  • Preferred crystalline phyllosilicates are those in which x in the abovementioned general formula assumes the values 2 or 3.
  • both .beta.- and ⁇ -sodium (Na 2 Si 2 O 5 ⁇ yH 2 O) are preferred, with beta-sodium disilicate being obtainable, for example, by the method described in the international patent application WO 91/08171 is described.
  • ⁇ -Sodium silicates with a modulus between 1.9 and 3.2 can according to the Japanese Patentarimmeldungen JP 04/238 809 or JP 04/260 610 getting produced.
  • Crystalline sodium silicates with a modulus ranging from 1.9 to 3.5, as prepared by the methods of European patents EP 0 164 552 and or EP 0 294 753 are available are used in a further preferred embodiment of the invention means.
  • Crystalline layer-form silicates of formula (I) given above are sold by Clariant GmbH under the trade name Na-SKS, eg Na-SKS-1 (Na 2 Si 22 O 45 .H 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 eg Na-SKS-1 (Na 2 Si 22 O 45 .H 2 O, Kenyaite)
  • Na-SKS-2 Na 2 Si 14 O 29 .xH 2 O, magadiite
  • Na-SKS-5 ⁇ -Na 2 Si 2 O 5
  • Na-SKS-7 ⁇ -Na 2 Si 2 O 5 , natrosilite
  • Na-SKS-9 NaHSi 2 O 5 3H 2 O
  • 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
  • compositions according to the invention a granular compound of crystalline phyllosilicate and citrate, of crystalline phyllosilicate and of the abovementioned (co) polymeric polycarboxylic acid, as described, for example, in the German patent application DE 198 19 187 or from alkali silicate and alkali carbonate, as described for Example in the international patent application WO 95/22592 or as it is commercially available, for example, under the name Nabion® 15.
  • Builder substances are preferably present in the compositions according to the invention in amounts of up to 75% by weight, in particular 5% by weight to 50.
  • suitable peroxygen compounds are in particular organic peracids or pers acid salts of organic acids, such as phthalimidopercaproic acid, perbenzoic acid or salts of diperdodecanedioic acid, hydrogen peroxide and under the washing conditions hydrogen peroxide donating inorganic salts, which include perborate, percarbonate, persilicate and / or persulfate Caroat belong into consideration.
  • organic peracids or pers acid salts of organic acids such as phthalimidopercaproic acid, perbenzoic acid or salts of diperdodecanedioic acid, hydrogen peroxide and under the washing conditions hydrogen peroxide donating inorganic salts, which include perborate, percarbonate, persilicate and / or persulfate Caroat belong into consideration.
  • solid peroxygen compounds are to be used, they can be used in the form of powders or granules, which can also be enveloped in a manner known in principle.
  • an agent according to the invention contains peroxygen compounds, they are present in amounts of preferably up to 50% by weight, in particular from 5% by weight to 30% by weight.
  • bleach stabilizers such as phosphonates, borates or metaborates and metasilicates and magnesium salts such as magnesium sulfate may be useful.
  • bleach activators it is possible to use compounds which, under perhydrolysis conditions, give aliphatic peroxycarboxylic acids having preferably 1 to 10 C atoms, in particular 2 to 4 C atoms, and / or optionally substituted perbenzoic acid.
  • Suitable substances are those which carry O- and / or N-acyl groups of the stated C atom number and / or optionally substituted benzoyl groups.
  • polyacylated alkylenediamines in particular tetraacetylethylenediamine (TAED), acylated triazine derivatives, in particular 1,5-diacetyl-2,4-dioxohexahydro-1,3,5-triazine (DADHT), acylated glycolurils, in particular tetraacetylglycoluril (TAGU), N- Acylimides, in particular N-nonanoylsuccinimide (NOSI), acylated phenolsulfonates, in particular n-nonanoyl or isononanoyloxybenzenesulfonate (n- or iso-NOBS), carboxylic anhydrides, in particular phthalic anhydride, acylated polyhydric alcohols, in particular triacetin, ethylene glycol diacetate, 2,5-diacetoxy- 2,5-dihydrofuran and from the German patent applications DE
  • Such bleach activators can, in particular in the presence of the abovementioned hydrogen peroxide-producing bleach, in the usual amount range, preferably in amounts of from 0.5 wt .-% to 10 wt .-%, in particular 1 wt .-% to 8 wt .-%, based on However, total agent, be included, missing when using percarboxylic acid as the sole bleach, preferably completely.
  • Suitable enzymes which can be used in the compositions are those from the class of amylases, proteases, lipases, cutinases, pullulanases, hemicellulases, cellulases, oxidases, laccases and peroxidases and mixtures thereof. Particularly suitable are from fungi or bacteria, such as Bacillus subtilis, Bacillus licheniformis, Bacillus lentus, Streptomyces griseus, Humicola lanuginosa, Humicola insolens, Pseudomonas pseudoalcaligenes, Pseudomonas cepacia or Coprinus cinereus derived enzymatic agents.
  • the enzymes can be as described, for example, in the European patent EP 0 564 476 or in the international patent application WO 94/23005 be adsorbed to carriers and / or embedded in encapsulating substances to protect against premature inactivation. They are in the washing or Detergents preferably in amounts up to 5 wt .-%, in particular from 0.2 wt .-% to 4 wt .-%, contain. If the agent of the invention contains protease, it preferably has a proteolytic activity in the range of about 100 PE / g to about 10,000 PE / g, in particular 300 PE / g to 8000 PE / g.
  • organic solvents which can be used in addition to water include alcohols having 1 to 4 C atoms, in particular methanol, ethanol, isopropanol and tert-butanol, diols having 2 to 4 C -Atomen, in particular ethylene glycol and propylene glycol, and mixtures thereof and derived from the classes of compounds mentioned ether.
  • Such water-miscible solvents are preferably present in the compositions according to the invention in amounts of not more than 30% by weight, in particular from 6% by weight to 20% by weight.
  • the compositions according to the invention may contain system and environmentally acceptable acids, in particular citric acid, acetic acid, tartaric acid, malic acid, lactic acid, glycolic acid, succinic acid, glutaric acid and / or adipic acid, but also mineral acids, in particular sulfuric acid, or bases, in particular ammonium or alkali metal hydroxides.
  • Such pH regulators are present in the compositions according to the invention in amounts of preferably not more than 20% by weight, in particular from 1.2% by weight to 17% by weight.
  • Graying inhibitors have the task of keeping suspended from the textile fiber dirt suspended in the fleet.
  • Water-soluble colloids of mostly organic nature are suitable for this purpose, for example starch, glue, gelatin, salts of ether carboxylic acids or ether sulfonic acids of starch or of cellulose or salts of acidic sulfuric acid esters of cellulose or starch.
  • water-soluble, containing acidic groups Polyamides are suitable for this purpose.
  • starch derivatives can be used, for example aldehyde starches.
  • cellulose ethers such as carboxymethylcellulose (Na salt), methylcellulose, hydroxyalkylcellulose and mixed ethers, such as methylhydroxyethylcellulose, methylhydroxypropylcellulose, methylcarboxymethylcellulose and mixtures thereof, for example in amounts of from 0.1 to 5% by weight, based on the compositions.
  • Detergents according to the invention may contain, for example, derivatives of diaminostilbenedisulfonic acid or their alkali metal salts as optical brighteners, although they are preferably free of optical brighteners for use as color detergents.
  • Suitable salts are, for example, salts of 4,4'-bis (2-anilino-4-morpholino-1,3,5-triazinyl-6-amino) stilbene-2,2'-disulphonic acid or compounds of similar construction which, instead of the morpholino Group carry a diethanolamino group, a methylamino group, an anilino group or a 2-methoxyethylamino group.
  • brighteners of the substituted diphenylstyrene type may be present, for example, the alkali salts of 4,4'-bis (2-sulfostyryl) -diphenyl, 4,4'-bis (4-chloro-3-sulfostyryl) -diphenyl, or 4 - (4-chlorostyryl) -4 '- (2-sulfostyryl).
  • Mixtures of the aforementioned optical brightener can be used.
  • foam inhibitors are, for example, soaps of natural or synthetic origin, which have a high proportion of C 18 -C 24 fatty acids.
  • Suitable non-surfactant foam inhibitors are, for example, organopolysiloxanes and mixtures thereof with microfine, optionally silanized silica and paraffins, waxes, microcrystalline waxes and mixtures thereof with silanated silicic acid or bis-fatty acid alkylenediamides. It is also advantageous to use mixtures of various foam inhibitors, for example those of silicones, paraffins or waxes.
  • the foam inhibitors, in particular silicone- and / or paraffin-containing foam inhibitors are preferably bound to a granular, water-soluble or dispersible carrier substance. In particular, mixtures of paraffins and bistearylethylenediamide are preferred.
  • compositions according to the invention presents no difficulties and can be carried out in a known manner, for example by spray-drying or granulation, enzymes and possibly other thermally sensitive ingredients such as, for example, bleaching agents optionally being added separately later.
  • inventive compositions having an increased bulk density in particular in the range of 650 g / l to 950 g / l, is one of the European patent EP 0 486 592 known method comprising an extrusion step is preferred.
  • Another preferred preparation by means of a granulation process is in the European patent specification EP 0 642 576 described.
  • compositions according to the invention in tablet form, which may be monophasic or multiphase, monochromatic or multicolor and in particular consist of one or more layers, in particular two layers
  • the procedure is preferably such that all constituents - if appropriate one per layer - in one Mixer mixed together and the mixture by means of conventional tablet presses, such as eccentric or rotary presses, pressed with compressive forces in the range of about 50 to 100 kN, preferably at 60 to 70 kN.
  • a tablet produced in this way has a weight of 10 g to 50 g, in particular 15 g up to 40 g.
  • the spatial form of the tablets is arbitrary and can be round, oval or angular, with intermediate forms are also possible. Corners and edges are advantageously rounded. Round tablets preferably have a diameter of 30 mm to 40 mm.
  • the size of rectangular or cuboid-shaped tablets, which are introduced predominantly via the metering device, for example the dishwasher, is dependent on the geometry and the volume of this metering device.
  • Exemplary preferred embodiments have a base area of (20 to 30 mm) x (34 to 40 mm), in particular of 26x36 mm or 24x38 mm.
  • Liquid or pasty compositions according to the invention in the form of customary solvent-containing solutions are generally prepared by simply mixing the ingredients, which can be added in bulk or as a solution in an automatic mixer.
  • Example 1 Preparation of 2,4-bis (3-carboxyphenylamino) -6-chlorotriazine.
  • 5-Aminoisophthalic acid (98%, 20g, 0.108 mol) was dissolved in a mixture of water (200 ml) and ice (20 g) and sodium hydroxide.
  • a freshly prepared suspension of cyanuric chloride (10 g, 0.054 mol) in ice / acetone (ca, 50 ml) was added with stirring at 0 ° C to 5 ° C and the pH was maintained at 6.5. After 4 hours, the mixture was warmed to 30 ° C. and the temperature was kept there for 16 hours, at pH 6.5. Phosphate buffer mixture and then acetone were added. The precipitated colorless solid was separated (yield 57 g, 53% purity).
  • Each of the triazine derivatives prepared in Examples 1 to 5 was applied by force to dipping on white cotton fabrics with the aid of an aqueous solution and the white textile was then washed with dyed textiles at 60 ° C. with a powder transfer detergent-free powder detergent.

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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)
  • Detergent Compositions (AREA)

Claims (8)

  1. Agent de lavage contenant un inhibiteur du transfert des couleurs sous la forme d'un dérivé de triazine répondant à la formule générale II

            X-NH-CH2CH2-(NY-CH2CH2-)nNH-X     (II)

    dans laquelle
    X représente un groupe -T(NH-Ar(CO2M)a)bHalc-1;
    T représente un groupe 1,3,5-triazinyle ;
    Ar représente un groupe phényle ;
    M représente un atome d'hydrogène, un atome de sodium, un atome de lithium ou un atome de potassium ;
    Hal représente un atome de chlore, un atome de brome ou un atome d'iode ;
    a est égal à 1, 2 ou 3 ;
    b est égal à 1 et c est égal à 2 ou bien b est égal à 2 et c est égal à 1 ;
    Y représente un atome d'hydrogène ou un groupe X ;
    et n représente un nombre de 0 à 50, à côté d'ingrédients habituels compatibles avec ce constituant.
  2. Agent selon la revendication 1, caractérisé en ce que l'on peut obtenir le dérivé de triazine par mise en réaction de 2 équivalents de composés répondant à la formule 1

            T(NH-Ar(CO2M)a)bHalc      (I)

    dans laquelle
    T représente un groupe 1,3,5-triazinyle ;
    Ar représente un groupe phényle ;
    M représente un atome d'hydrogène, un atome de sodium, un atome de lithium ou un atome de potassium ;
    Hal représente un atome de chlore, un atome de brome ou un atome d'iode ;
    a est égal à 1, 2 ou 3 ;
    b est égal à 1 et c est égal à 2 ou bien b est égal à 2 et c est égal à 1 ;
    avec du 1,2-diaminoéthane ou bien avec une oligo-éthylènimine ou une polyéthylènimine.
  3. Agent selon la revendication 2, caractérisé en ce que l'oligo-éthylènimine ou la polyéthylènimine répond à la formule NH2-CH2CH2-(NH-CH2CH2-)nNH2, dans laquelle n représente un nombre de 1 à 30, en particulier de 2 à 20.
  4. L'agent selon l'une quelconque des revendications 1 à 3, caractérisé en ce qu'il contient, à concurrence de 0,05 % en poids à 2 % en poids, en particulier de 0,2 % en poids à 1 % en poids, un dérivé de triazine inhibant le transfert des couleurs, répondant à la formule générale I et/ou II.
  5. L'agent selon l'une quelconque des revendications 1 à 4, caractérisé en ce qu'il contient en outre un polymère choisi parmi la vinylpyrrolidone, le vinylimidazole, un N-oxyde de vinylpyridine ou un de leurs copolymères.
  6. Utilisation de dérivés de triazine répondant à la formule générale I ou II :

            T(NH-Ar(CO2Ma)bHalc      (I)

            X-NH-CH2CH2-(NY-CH2CH2-)nNH-X     (II)

    dans lesquelles
    T représente un groupe 1,3,5-triazinyle ;
    Ar représente un groupe phényle ;
    M représente un atome d'hydrogène, un atome de sodium, un atome de lithium ou un atome de potassium ;
    Hal représente un atome de chlore, un atome de brome ou un atome d'iode ;
    a est égal à 1, 2 ou 3 ;
    b est égal à 1 et c est égal à 2 ou bien b est égal à 2 et c est égal à 1 ;
    X représente un groupe -T(NH-Ar(CO2M)a)bHalc-1;
    Y représente un atome d'hydrogène ou un groupe X ;
    et n représente un nombre de 0 à 50,
    pour éviter le transfert de colorants de textiles à partir de textiles colorés sur des textiles non colorés ou possédant une autre couleur, lors de leur lavage conjoint dans des solutions aqueuses en particulier contenant des agents tensioactifs.
  7. Utilisation de dérivés de triazine répondant à la formule générale I ou II :

            T(NH-Ar(CO2M)a)bHalc      (I)

            X-NH-CH2CH2-(NY-CH2CH2-)nNH-X     (II)

    dans lesquelles
    T représente un groupe 1,3,5-triazinyle ;
    Ar représente un groupe phényle ;
    M représente un atome d'hydrogène, un atome de sodium, un atome de lithium ou un atome de potassium ;
    Hal représente un atome de chlore, un atome de brome ou un atome d'iode ;
    a est égal à 1, 2 ou 3 ;
    b est égal à 1 et c est égal à 2 ou bien b est égal à 2 et c est égal à 1 ;
    X représente un groupe -T(NH-Ar(CO2M)a)bHalc-1 ;
    Y représente un atome d'hydrogène ou un groupe X ;
    et n représente un nombre de 0 à 50,
    pour éviter la modification de l'impression de couleur que laissent des textiles colorés, lors de leur lavage dans des solutions aqueuses en particulier contenant des agents tensioactifs.
  8. Procédé pour le lavage des textiles dans des solutions aqueuses contenant des agents tensioactifs, caractérisé en ce qu'on met en oeuvre une solution aqueuse contenant un ou plusieurs agents tensioactifs, qui contient un dérivé de triazine répondant à la formule générale II.
EP07703336A 2006-03-14 2007-02-08 Lessive protégeant les couleurs Not-in-force EP1994133B1 (fr)

Priority Applications (1)

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DE102006012018A DE102006012018B3 (de) 2006-03-14 2006-03-14 Farbschützendes Waschmittel
PCT/EP2007/001054 WO2007104392A1 (fr) 2006-03-14 2007-02-08 Lessive protégeant les couleurs

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EP (1) EP1994133B1 (fr)
JP (1) JP5143752B2 (fr)
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EP3747979A1 (fr) 2019-06-05 2020-12-09 Glatfelter Gernsbach GmbH Tissu non tissé capturant les colorants et son procédé de production
CN118223037B (zh) * 2024-04-25 2024-11-15 广东粤首新科技有限公司 一种含表面活性剂的清洗剂和制备方法

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DE102006012018B3 (de) 2007-11-15
JP5143752B2 (ja) 2013-02-13
JP2009529593A (ja) 2009-08-20
EP1994133A1 (fr) 2008-11-26
US7947087B2 (en) 2011-05-24
PL1994133T3 (pl) 2011-09-30
ATE507279T1 (de) 2011-05-15
US20090069210A1 (en) 2009-03-12
ES2362017T3 (es) 2011-06-27

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