EP0596968A1 - Agent for treating washed clothes in a clothes drier - Google Patents

Agent for treating washed clothes in a clothes drier

Info

Publication number
EP0596968A1
EP0596968A1 EP92916357A EP92916357A EP0596968A1 EP 0596968 A1 EP0596968 A1 EP 0596968A1 EP 92916357 A EP92916357 A EP 92916357A EP 92916357 A EP92916357 A EP 92916357A EP 0596968 A1 EP0596968 A1 EP 0596968A1
Authority
EP
European Patent Office
Prior art keywords
component
fatty
composition according
mixtures
fatty acid
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.)
Withdrawn
Application number
EP92916357A
Other languages
German (de)
French (fr)
Inventor
Rolf Puchta
Peter Sandkühler
Jutta Schreiber
Theodor Völkel
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
Publication of EP0596968A1 publication Critical patent/EP0596968A1/en
Withdrawn legal-status Critical Current

Links

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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/04Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
    • C11D17/041Compositions releasably affixed on a substrate or incorporated into a dispensing means
    • C11D17/047Arrangements specially adapted for dry cleaning or laundry dryer related applications
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2093Esters; Carbonates
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/005Compositions containing perfumes; Compositions containing deodorants
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/144Alcohols; Metal alcoholates
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165Ethers
    • D06M13/17Polyoxyalkyleneglycol ethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/188Monocarboxylic acids; Anhydrides, halides or salts thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224Esters of carboxylic acids; Esters of carbonic acid
    • D06M13/2243Mono-, di-, or triglycerides
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/722Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40Reduced friction resistance, lubricant properties; Sizing compositions
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2352Coating or impregnation functions to soften the feel of or improve the "hand" of the fabric

Definitions

  • the present invention relates to an agent for treating washed laundry in a tumble dryer consisting of a flexible surface that is loaded with an active substance mixture for laundry treatment.
  • Treating washed laundry in this way generally aims to give the laundry a pleasantly soft and full feel, as well as anti-electrostatic properties and a good fragrance.
  • the treatment of the laundry in the rinsing bath relied on the use of active substances which are transferred as completely as possible to the textiles to be treated in an aqueous liquor, the fact that the treatment process was relocated to the tumble dryer made it possible to also use such active substances which were difficult or impossible to use in an aqueous liquor.
  • DE-A 1967470 the disadvantages described are to be avoided by using substrates with a medium adsorption capacity as carriers for the quaternary ammonium compounds. It was later found, however, that under certain conditions it is also possible to use substrates with a low adsorption capacity, which have the advantage of the high release of active ingredient, without the formation of stains.
  • DE-A 3003249 relates to agents for treating washed laundry in a laundry dryer, the carriers of which for the softening active ingredients comprise a substrate with a low adsorption capacity.
  • Another object is to provide a textile-softening active substance or mixture of active substances which, during production after application to the flexible fabric, solidifies quickly, that is to say at a relatively high temperature, to a dry-feeling active substance layer and the textiles treated therewith have good antielectrostatic properties Gives properties.
  • the present invention therefore relates to agents for treating washed laundry in a tumble dryer, consisting of a flexible sheet loaded with active ingredient mixtures for laundry treatment, the active ingredient mixtures containing a fat component which are characterized in that the mono-, di Fat component a) in a mixture with b) fatty alcohol alkoxylates and / or fatty acid esters of monohydric alcohols is present - or trifatty acid glycerides and / or fatty acids and / or fatty alcohols.
  • the constituents of the fat component a) are known per se as softening active ingredients, but these alone or in combination do not meet the requirements which are described in more detail in the description of the object of the present invention. They are either difficult to process because they solidify too slowly or too quickly when they are applied to the flexible surface; or they do not impart sufficient softness or sufficient anti-electrostatic properties to the textiles treated with them; or the flexible sheets coated with it feel uncomfortable, which prevents the consumer from using them; or the drug delivery rate is too low.
  • the fat component a) with component b), the monovalent of fatty alcohol alkoxylates and / or Fettklaestern alcohols is, in such a way that the active ingredient mixtures formed have a crystallization onset is r at a temperature of 40 ° C or higher.
  • the start of crystallization in the sense of this patent application is determined by DSC measurement using a device from Mettler, type FP 84.
  • the active substance mixture to be tested is heated at a heating rate of 2 ° C. per minute until the melting end temperature is reached.
  • the Temperature at which crystallization begins the heat of crystallization given off.
  • the temperature at which the heat of crystallization begins to be given is called the start of crystallization below.
  • Mixtures of active ingredients from components a) and b) which are suitable for the treatment agents according to the invention have an onset of crystallization at a temperature of 40 ° C. or higher.
  • the active ingredient mixtures contain a fat component a) which contains mono- and di-fatty acid glyceride, preferably mono-fatty acid glycerides.
  • the fatty acid residue of these mono- and diglycerides is derived from fatty acids which can be straight-chain or branched, saturated or unsaturated and contain 10 to 24 carbon atoms.
  • a typical example of suitable glyceride mixtures is, for example, a mixture consisting of mono- and di-fatty acid glyceride which predominantly contains mono-fatty acid glyceride and whose fatty acid residue is derived from stearic acid.
  • a glycerol mono-di-palmitate / stearate is also suitable, the proportion of monoglyceride being 40 to 60%.
  • a preferred embodiment of the agents according to the invention contains in fatty component a) fatty acids with a melting point in the range from 40 to 80, preferably in the range from 45 to 65 ° C.
  • the fatty acids can be of natural and synthetic origin and are generally straight-chain and in particular saturated. Natural fatty acids are derived from triglycerides, for example from coconut oil, palm kernel oil, olive oil or also from animal fats such as beef tallow, fish oil or lard. Depending on their origin, the fatty acids derived therefrom are mixtures of different fatty acids and are also preferred if, after hydrogenation if necessary, they have a melting point in the range from 40 to 80, in particular in the range from 45 to 65 ° C.
  • the fat component a) can also contain fatty alcohols.
  • Fatty alcohols preferred for the agents according to the invention have 10 to 22 carbon atoms in the molecule.
  • the fatty alcohol alkoxylates suitable for component b) are generally based on the fatty alcohols, as are also suitable for the fatty component a). They contain 1 to 15 moles of ethylene oxide and / or 1 to 15 moles of propylene oxide per mole of fatty alcohol. Fatty alcohol alkoxylates in which ethylene oxide and propylene oxide are simultaneously attached to the fatty alcohol are preferred. In particular, suitable fatty alcohol alkoxylates contain 2 to 8 moles of ethylene oxide and / or propylene oxide per mole of fatty alcohol.
  • component b) may contain fatty acid esters of monohydric alcohols.
  • Preferred fatty acid esters of monohydric alcohols contain a total of 15 to 44 carbon atoms.
  • Monovalent "alcohol component in particular methyl alcohol, ethyl alcohol are n-propyl and iso-propyl alcohol in question.
  • Fettklarekompo ⁇ the appropriate fatty acid ester component of monovalent alcohols, the same applies as already explained above for the fatty acids.
  • fatty acid ester of monohydric alcohols are within the scope of The present invention is also understood to mean mixtures of fatty acid esters of various compositions, for example carnauba wax obtainable from the leaves of the Brazilian fan palm Copernica prunivera, candeliol wax obtained from the leaves of Euphorbiaceae, jojoba oil and natural or synthetic beeswax ⁇ a mixture in question, the 40 parts by weight of a fatty acid onoglyceride, the acid component of which is a 3: 1 mixture of hydroxystearic acid and hardened castor oil, and 35 parts by weight of palmitic acid, 20 Parts by weight of micro wax, 10 parts by weight of hydroxystearic acid and other constituents in minor amounts.
  • Such natural ester mixtures are also counted among the fatty acid esters of monohydric alcohols in the context of the present invention.
  • Mixtures have the preferred start of crystallization at a temperature of 40 ° C or higher, the active ingredient mixtures consist of component a) and component b) in a weight ratio of 3: 1 to 1: 3, preferably in a weight ratio of 2: 1 to 1: 2.
  • Agents according to the invention in which the active compound mixtures contain component a) and component b) in the weight ratio mentioned are preferred moves.
  • the addition of an effective amount of glycerol which generally makes up 1 to 15% by weight, based on the active ingredient mixtures, is particularly suitable for this purpose.
  • the flexible sheet materials used as carriers for the active substance mixture may contain an amount of the active substance mixtures which is sufficient for a single application or for repeated use, it is preferred that the agents have an amount which is sufficient for a single application contain components a) + b). This is preferably an amount of 1 to 5 g, which is applied to the flexible fabric on one or both sides.
  • the active ingredient mixtures are liquefied by heating.
  • Particularly suitable mixtures of active ingredients have a viscosity of 5 to 100 mPas at 60 ° C .; they are therefore preferred.
  • the flash point of the active substance mixtures is significantly higher than that for the known compositions for the treatment of washed laundry in general Dryer mixtures used active ingredients.
  • Agents according to the invention the active ingredient mixtures of which have a flash point of more than 55 ° C., preferably more than 100 ° C., are therefore particularly preferred.
  • Such a high flash point has a particularly favorable effect on the production of the agents according to the invention, in which the active substance mixtures are applied to the flexible fabric at elevated temperature.
  • the flexible surface structure of the agents according to the invention can be a fibrous surface structure and accordingly a woven, a knitted one textile material or a non-woven fabric.
  • Foam or sponge-like materials of natural or synthetic origin such as foamed synthetic polymers, which are preferably in sheet form, are also suitable as flexible fabrics.
  • the textile fabrics generally have a lower adsorption capacity than the foam or sponge-like materials. The lower adsorption capacity is usually associated with a high rate of release of the active ingredient mixtures, whereas the foam or sponge-like materials can absorb more of the active ingredient mixture, but generally release it less completely when used in the tumble dryer. Above all, the flexible textile fabrics, and in particular the non-woven fabrics, have proven successful.
  • a carrier for the active ingredient mixtures are flexible fabrics which are a nonwoven made of synthetic and natural fiber materials.
  • compositions according to the invention do not contain any salt-like constituents, such as quaternary ammonium salts, in their active ingredient mixtures
  • the textiles treated with the compositions according to the invention have surprisingly good antielectrostatic properties after treatment in a tumble dryer, which takes place at temperatures of about 50 to 80 ° C. ⁇ shafts.
  • the agents according to the invention convince through the sum of the desirable properties present. They are easy to manufacture, do not feel uncomfortable after manufacture, have the property of releasing the active substance mixtures almost completely when used in the tumble dryer and transferring them to the textiles to be treated, and they give the textiles to be treated a pleasantly soft and full grip and excellent anti-electrostatic properties.
  • the active ingredient mixtures are also free of quaternary ammonium compounds, the environmental impact from the active ingredients which enter the sewer system with the washing water of the laundry following treatment in the tumble dryer is extremely low.
  • Another advantage of the agents according to the invention is the fact that the in the components present in the active ingredient mixture are produced from natural and renewable raw materials.
  • the active substance mixtures can additionally contain customary auxiliaries and additives in agents for treating washed laundry in a tumble dryer. These are, for example, fragrances, dyes, heavy metal complexing agents, clay materials or finely divided silica.
  • the start of crystallization for mixture A was 42 ° C, that for mixture B at 46 ° C.
  • DMDMAC distearyldimethylammonium chloride
  • the flash point of mixture A was 166 ° C, for mixture B 156 ° C, whereas for the DSDMAC mixture it was 28 ° C. Accordingly, the DSDMAC mixture is to be treated as dangerous goods, but the active substance mixtures A and B of the agents according to the invention are not. Textiles treated with this had an approximately equally good grip in all cases.
  • the anti-electrostatic properties measured as the half-life of the dissipation of an applied electrical charge, were 7.6 seconds (A) and 10.6 seconds (B) and 36 seconds DSDMAC.
  • the toxicological, ecological and ecotoxicological behavior of the active substance mixtures A and B was better than that of DSDMAC in every respect.

Abstract

Un produit contient sur un support plat flexible une combinaison de glycérides d'acides gras, d'acides gras et/ou d'alcools gras d'une part et d'alcoxylates d'alcools gras et/ou d'esters d'acides gras d'alcools monovalents d'autre part, servant de mélange adoucissant de matières textiles.A product contains on a flexible flat support a combination of glycerides of fatty acids, fatty acids and / or fatty alcohols on the one hand and alkoxylates of fatty alcohols and / or esters of fatty acids monovalent alcohols on the other hand, serving as a softening mixture of textile materials.

Description

"Mittel zum Behandeln gewaschener Wäsche in einem Wäschetrockner""Means for treating washed laundry in a tumble dryer"
Die vorliegende Erfindung betrifft ein Mittel zum Behandeln gewaschener Wäsche in einem Wäschetrockner bestehend aus einem flexiblen Flächenge¬ bilde, das mit einem Wirkstoffgemisch zur Wäschebehandlung beladen ist.The present invention relates to an agent for treating washed laundry in a tumble dryer consisting of a flexible surface that is loaded with an active substance mixture for laundry treatment.
Mit der Entwicklung von automatischen Wäschetrocknern, in denen gewaschene Wäsche durch erwärmte Luft getrocknet wird, bot sich die Möglichkeit, eine sonst im allgemeinen während des letzten Spülgangs in der Waschmaschine vorgenommene Behandlung der Wäsche im Wäschetrockner vorzunehmen. Eine derartige Behandlung gewaschener Wäsche zielt in der Regel darauf ab, der Wäsche einen angenehmen weichen und vollen Griff sowie antielektrosta¬ tische Eigenschaften und einen guten Duft zu vermitteln. Während man bei der Behandlung der Wäsche im Spülbad darauf angewiesen war, Wirkstoffe zu verwenden, die in wässeriger Flotte möglichst vollständig auf die zu be¬ handelnden Textilien übertragen werden, ergab sich durch die Verlagerung des Behandlungsprozesses in den Wäschetrockner die Möglichkeit, auch solche Wirkstoffe einzusetzen, die in wässeriger Flotte nur schwer bezie¬ hungsweise nicht einsetzbar waren. Wenn man auch grundsätzlich bei der Behandlung der Wäsche im Wäschetrockner die Möglichkeit hat, andere Wirk¬ stoffe, als man sie bei der Behandlung im Spülbad verwendet, einzusetzen, hat man doch bisher fast ausschließlich die auch bei der Behandlung im Spülbad verwendeten Wirkstoffe vom Typ der sich von Ammoniak oder Imidazolin ableitenden quartären Ammoniumverbindungen mit 1, 2 oder 3 langen Resten im Molekül auch bei der Behandlung der Wäsche im Wäsche¬ trockner eingesetzt. Der Grund hierfür ist, daß derartige quartäre Ammoniumverbindungen auf synthetischem Wege verhältnismäßig leicht zugäng¬ lich sind und vor allem, daß sie als TextilWeichmacher ausgezeichnet wirk¬ sam sind. Für die Applikation der weichmachenden Wirkstoffe auf die Textilien im Wäschetrockner sind verschiedene Vorschläge bekannt geworden; so wurde beispielsweise vorgeschlagen, die Wirkstoffe, gewünschtenfalls zusammen mit zusätzlichen Hilfsstoffen, aus starren Behältern, die der Wäsche im Wäschetrockner beigegeben werden, auf die Wäsche zu übertragen. Anstelle der starren Behälter sind auch flexible Behälter, beispielsweise Beutel, vorgeschlagen worden, die mit den Wirkstoffen gefüllt sind. Am einfachsten und daher auch im allgemeinen am gebräuchlichsten ist aber die Abgabe der Wirkstoffe von flexiblen Flächengebilden. Die Behandlung von Wäsche im Wäschetrockner durch mit Wirkstoffen imprägnierte flexible Flächengebilde ist beispielsweise in der deutschen Patentanmeldung DE-A 19 55 803 be¬ schrieben. Je nach der Art der verwendeten textilen Flächengebilde, die mit dem Wirkstoff imprägniert sind, ergibt sich aber das Problem, daß bei Substraten mit niedriger Adsorptionskapazität die fettartigen Wirkstoff^ ungleichmäßig auf die Textilien übertragen werden und dabei zu fettfleck¬ artigen Störungen führen. Andere Substratmaterialien mit hoher Adsorp¬ tionskapazität, wie beispielsweise Schwammtücher oder Schaumstoffplatten geben die Wirkstoffe nur in unzureichendem Maße frei, so daß es bei deren Verwendung als Wirkstoffträger zu Wirkstoffverlusten durch nicht ausge¬ nutzte Wirkstoffe kommt.With the development of automatic tumble dryers, in which washed laundry is dried by heated air, it became possible to carry out the laundry in the tumble dryer, which was generally carried out in the washing machine during the last rinse cycle. Treating washed laundry in this way generally aims to give the laundry a pleasantly soft and full feel, as well as anti-electrostatic properties and a good fragrance. While the treatment of the laundry in the rinsing bath relied on the use of active substances which are transferred as completely as possible to the textiles to be treated in an aqueous liquor, the fact that the treatment process was relocated to the tumble dryer made it possible to also use such active substances which were difficult or impossible to use in an aqueous liquor. Although it is possible in principle to use laundry agents in the tumble dryer to use other active substances than those used in the treatment in the rinsing bath, the active substances of the type which have also been used almost exclusively in the treatment in the rinsing bath have hitherto been used Quaternary ammonium compounds with 1, 2 or 3 long residues in the molecule which are derived from ammonia or imidazoline are also used in the treatment of laundry in the clothes dryer. The reason for this is that such quaternary ammonium compounds are relatively easily accessible by synthetic means and, above all, that they are extremely effective as textile softeners. Various proposals have become known for the application of the softening active ingredients to the textiles in the tumble dryer; it has been proposed, for example, to transfer the active ingredients, if desired together with additional auxiliaries, to the laundry from rigid containers which are added to the laundry in the tumble dryer. Instead of the rigid containers, flexible containers, for example bags, which have been filled with the active substances have also been proposed. The simplest and therefore also the most common in general is the delivery of the active ingredients from flexible fabrics. The treatment of laundry in a tumble dryer by flexible fabrics impregnated with active ingredients is described, for example, in German patent application DE-A 19 55 803. Depending on the type of textile fabrics used, which are impregnated with the active ingredient, the problem arises that in the case of substrates with a low adsorption capacity, the fatty active ingredient is transferred unevenly to the textiles and in the process leads to grease-stained disorders. Other substrate materials with a high adsorption capacity, such as, for example, sponge cloths or foam sheets, release the active substances to an insufficient extent, so that when they are used as active substance carriers, active substance losses due to unused active substances occur.
Nach der Lehre der DE-A 1965470 sind die geschilderten Nachteile zu ver¬ meiden, indem man als Träger für die quartären Ammoniumverbindungen Substrate mit einer mittleren Adsorptionskapazität verwendet. Später wurde allerdings festgestellt, daß man unter bestimmten Bedingungen auch Substrate mit einer niedrigen Adsorptionskapazität, die den Vorteil der hohen Wirkstoffabgäbe aufweisen, verwenden kann, ohne daß es zu Flecken¬ bildungen kommt. Mittel zum Behandeln gewaschener Wäsche im einem Wäsche¬ trockner, deren Träger für die weichmachenden Wirkstoffe ein Substrat mit niedriger Adsorptionskapazität umfassen, sind Gegenstand der DE-A 3003249.According to the teaching of DE-A 1965470, the disadvantages described are to be avoided by using substrates with a medium adsorption capacity as carriers for the quaternary ammonium compounds. It was later found, however, that under certain conditions it is also possible to use substrates with a low adsorption capacity, which have the advantage of the high release of active ingredient, without the formation of stains. DE-A 3003249 relates to agents for treating washed laundry in a laundry dryer, the carriers of which for the softening active ingredients comprise a substrate with a low adsorption capacity.
Nach der Lehre der DE-A 2700512 lassen sich bis zu 60 % der weichmachen¬ den quartären Ammoniumverbindungen durch Fettsäureester eines mehrwertigen Alkohols ersetzen. Dies führt zu dem Vorteil, daß man offenbar nicht an eine bestimmte Adsorptionskapazität der als Wirkstoffträger verwendeten Substrate gebunden ist.According to the teaching of DE-A 2700512, up to 60% of the plasticizing quaternary ammonium compounds can be replaced by fatty acid esters of a polyhydric alcohol. This leads to the advantage that one does not appear to a certain adsorption capacity of the substrates used as active substance carriers is bound.
Es sind auch im Wäschetrockner anzuwendende Textilbehandlungsmittel be¬ kannt geworden, deren Wirkstoffe frei von quartären Ammoniumverbindungen sind. So beschreibt zum Beispiel die DE-A 25 16 104 Erzeugnisse, deren Wirkstoffkomponente zum Teil oder vollständig Sorbitanester sind. Diese neigen aber ebenso wie die quartären Ammoniumverbindungen zur Fleckenbil- dung beziehungsweise zur unzureichenden Wirkstoffabgäbe, wenn als Substrat nicht Materialien mit einer mittleren Adsorptionskapazität verwendet wer¬ den.There are also known textile treatment agents to be used in the tumble dryer, the active ingredients of which are free of quaternary ammonium compounds. For example, DE-A 25 16 104 describes products whose active ingredient components are partly or completely sorbitan esters. However, like the quaternary ammonium compounds, these tend to form stains or to give off insufficient active ingredient if materials with an average adsorption capacity are not used as the substrate.
Andere textilweichmachende Wirkstoffe, die keine quartären Ammoniumverbin¬ dungen darstellen, sind die beispielsweise aus der DE 27 00 512 bekannten Fettsäureester mehrwertiger Alkohole. Nach der Lehre dieser Patentanmel¬ dung müssen sie aber gemeinsam mit nennenswerten Mengen (40 bis 95 Gew.-%) kationischer Textilweichmacher vom Typ der quartären Ammoniumverbindungen zusammen verwendet werden. Quartäre Ammoniumverbindungen belasten aber nach neueren Erkenntnissen durch ihre mehr oder weniger stark ausgeprägten toxischen Eigenschaften und durch ihre geringe biologische Abbaubarkeit das Abwasser, in das sie durch den Spülgang beziehungsweise mit der Wasch¬ lauge des auf den Nachbehandlungsvorgang folgenden Waschprozesses gelan¬ gen. Es ist daher die Aufgabe der vorliegenden Erfindung, textilweich¬ machende Wirkstoffgemische für die Behandlung gewaschener Wäsche im Wäschetrockner bereitzustellen, wobei die Wirkstoff-Gemische ihrerseits ohne Fleckenbildung und mit hoher Abgaberate von einem als Träger für die Wirkstoffe dienenden flexiblen Flächengebilde abgegeben und auf die zu behandelnden Textilien übertragen werden und wobei die Wirkstoffgemische frei sind von quartären Ammoniumverbindungen. Eine weitere Aufgabe besteht in der Bereitstellung eines textilweich achenden Wirkstoffs beziehungs¬ weise Wirkstoffgemischs, das bei der Herstellung nach der Applikation auf das flexible Flächengebilde schnell, das heißt bei einer relativ hohen Temperatur zu einer sich trocken anfühlenden Wirkstoffschicht erstarrt und den damit behandelten Textilien gute antielektrostatische Eigenschaften verleiht. Es hat sich nun überraschenderweise herausgestellt, daß sich die als alleiniger textilweichmachender Wirkstoff ungeeigneten Fettsäureglyceride mit anderen, ebenfalls als alleinigen Textilweichmachern ungeeigneten Fettalkohol- beziehungsweise Fettsäure-Derivaten zu Wirkstoffgemischen kombinieren lassen, die die geschilderten Nachteile der bekannten Wirk- stoffgemische des Standes der Technik nicht haben und die übrigen wünschenswerten Anforderungen erfüllen.Other textile-softening active ingredients which are not quaternary ammonium compounds are the fatty acid esters of polyhydric alcohols known for example from DE 27 00 512. According to the teaching of this patent application, however, they must be used together with significant amounts (40 to 95% by weight) of cationic textile plasticizers of the quaternary ammonium compound type. Quaternary ammonium compounds, however, according to newer knowledge, pollute the wastewater due to their more or less pronounced toxic properties and their low biodegradability, into which they get through the rinse cycle or with the washing liquor of the washing process following the aftertreatment process. It is therefore the object of the present invention to provide textile-softening active substance mixtures for the treatment of washed laundry in a tumble dryer, the active substance mixtures in turn being emitted without stains and at a high release rate from a flexible fabric serving as a carrier for the active substances and being transferred to the textiles to be treated and wherein the active ingredient mixtures are free of quaternary ammonium compounds. Another object is to provide a textile-softening active substance or mixture of active substances which, during production after application to the flexible fabric, solidifies quickly, that is to say at a relatively high temperature, to a dry-feeling active substance layer and the textiles treated therewith have good antielectrostatic properties Gives properties. It has now surprisingly been found that the fatty acid glycerides which are unsuitable as the sole fabric softening active ingredient can be combined with other fatty alcohol or fatty acid derivatives which are likewise unsuitable as the sole fabric softener to form active ingredient mixtures which do not have the disadvantages described of the known active ingredient mixtures of the prior art and meet the other desirable requirements.
Gegenstand der vorliegenden Erfindung sind daher Mittel zum Behandeln ge¬ waschener Wäsche in einem Wäschetrockner, bestehend aus einem mit Wirk- stoffgemisehen zur Wäschebehandlung beladenen flexiblen Flächengebilde, wobei die Wirkstoffgemische eine Fettkomponente enthalten, die dadurch ge¬ kennzeichnet sind, daß die Mono-, Di- oder Trifettsäureglyceride und/oder Fettsäuren und/oder Fettalkohole umfassende Fettkomponente a) im Gemisch mit b) Fettalkohol-Alkoxylaten und/oder Fettsäureestern einwertiger Alkohole vorliegt.The present invention therefore relates to agents for treating washed laundry in a tumble dryer, consisting of a flexible sheet loaded with active ingredient mixtures for laundry treatment, the active ingredient mixtures containing a fat component which are characterized in that the mono-, di Fat component a) in a mixture with b) fatty alcohol alkoxylates and / or fatty acid esters of monohydric alcohols is present - or trifatty acid glycerides and / or fatty acids and / or fatty alcohols.
Die Bestandteile der Fettkomponente a) sind für sich als weichmachende Wirkstoffe bekannt, jedoch erfüllen diese für sich allein oder auch in Kombination miteinander nicht die Anforderungen, die in der Schilderung der Aufgabe der vorliegenden Erfindung näher beschrieben sind. So lassen sie sich entweder schlecht verarbeiten weil sie bei ihrer Aufbringung auf das flexible Flächengeb lde zu langsam oder zu schnell erstarren; oder sie verleihen den damit behandelten Textilien keine ausreichende Weichheit oder keine genügenden antielektrostatischen Eigenschaften; oder die damit beschichteten flexiblen Flächengebilde fühlen sich unangenehm an, was den Verbraucher hindert, sie zu verwenden; oder die Wirkstoffabgaberate ist zu gering. Man kombiniert daher die Fettkomponente a) mit einer Komponente b), die aus Fettalkohol-Alkoxylaten und/oder Fettsäureestern einwertiger Alkohole besteht, in der Weise, daß die gebildeten Wirkstoffgemische einen Kristallisationsbeginn habenr der bei einer Temperatur von 40 °C oder höher liegt. Der Kristallisationsbeginn im Sinne dieser Patentanmeldung wird bestimmt durch DSC-Messung mit einem Gerät der Firma Mettler, Typ FP 84. Das zu prüfende Wirkstoffgemisch wird mit einer Aufheizrate von 2 °C pro Minute bis zum Erreichen der Schmelzendpunkt-Temperatur aufgeheizt. Bei der sich anschließenden Abkühlung des Wirkstoffsgemisches wird bei der Temperatur, bei der die Kristallisation beginnt, die Kristallisationswär e abgegeben. Die Temperatur, bei der die Abgabe der Kristallisationswärme beginnt, wird im folgenden Kristallisationsbeginn genannt. Wirkstoffge¬ mische aus den Komponenten a) und b), die für die erfindungsgemäßen Be¬ handlungsmittel geeignet sind, haben einen Kristallisationsbeginn bei einer Temperatur von 40 °C oder höher.The constituents of the fat component a) are known per se as softening active ingredients, but these alone or in combination do not meet the requirements which are described in more detail in the description of the object of the present invention. They are either difficult to process because they solidify too slowly or too quickly when they are applied to the flexible surface; or they do not impart sufficient softness or sufficient anti-electrostatic properties to the textiles treated with them; or the flexible sheets coated with it feel uncomfortable, which prevents the consumer from using them; or the drug delivery rate is too low. Therefore, combining the fat component a) with component b), the monovalent of fatty alcohol alkoxylates and / or Fettsäureestern alcohols is, in such a way that the active ingredient mixtures formed have a crystallization onset is r at a temperature of 40 ° C or higher. The start of crystallization in the sense of this patent application is determined by DSC measurement using a device from Mettler, type FP 84. The active substance mixture to be tested is heated at a heating rate of 2 ° C. per minute until the melting end temperature is reached. During the subsequent cooling of the active ingredient mixture, the Temperature at which crystallization begins, the heat of crystallization given off. The temperature at which the heat of crystallization begins to be given is called the start of crystallization below. Mixtures of active ingredients from components a) and b) which are suitable for the treatment agents according to the invention have an onset of crystallization at a temperature of 40 ° C. or higher.
In einer bevorzugten Ausführungsform enthalten die Wirkstoffgemische eine Fettkomponente a), die Mono- und Di-Fettsäureglycerid, vorzugsweise Mono-Fettsäureglyceride enthält. Der Fettsäurerest dieser Mono- und Diglyceride leitet sich von Fettsäuren ab, die geradkettig oder verzweigt, gesättigt oder ungesättigt sein können und 10 bis 24 Kohlenstoffatome ent¬ halten. Ein typisches Beispiel für geeignete Glyceridgemische ist beispielsweise ein aus Mono- und Di-Fettsäureglycerid bestehendes Gemischr, das überwiegend Mono-Fettsäureglycerid enthält und dessen Fettsäurerest sich von Stearinsäure ableitet. Ebenfalls geeignet ist ein Glycerin-Mono- Di-Palmitat/Stearat, wobei der Anteil an Monoglycerid 40 bis 60 % beträgt.In a preferred embodiment, the active ingredient mixtures contain a fat component a) which contains mono- and di-fatty acid glyceride, preferably mono-fatty acid glycerides. The fatty acid residue of these mono- and diglycerides is derived from fatty acids which can be straight-chain or branched, saturated or unsaturated and contain 10 to 24 carbon atoms. A typical example of suitable glyceride mixtures is, for example, a mixture consisting of mono- and di-fatty acid glyceride which predominantly contains mono-fatty acid glyceride and whose fatty acid residue is derived from stearic acid. A glycerol mono-di-palmitate / stearate is also suitable, the proportion of monoglyceride being 40 to 60%.
Eine bevorzugte Ausführungsform der erfindungsgemäßen Mittel enthält in der Fettkomponente a) Fettsäuren mit einem Schmelzpunkt im Bereich von 40 bis 80, vorzugsweise im Bereich von 45 bis 65 °C. Die Fettsäuren können natürlichen und synthetischen Ursprungs sein und sind im allgemeinen geradkettig und insbesondere gesättigt. Natürliche Fettsäuren leiten sich von Triglyceriden ab, beispielsweise von Kokosöl, Palmkernöl, Olivenöl oder aber auch von tierischen Fetten wie Rindertalg, Fischöl, oder Schweineschmalz. Entsprechend ihrer Herkunft stellen die hieraus sich ab¬ leitenden Fettsäuren Gemische unterschiedlicher Fettsäuren dar und sind ebenfalls bevorzugt, sofern sie, gegebenenfalls nach Hydrierung, einen Schmelzpunkt im Bereich von 40 bis 80, insbesondere im Bereich von 45 bis 65 °C haben.A preferred embodiment of the agents according to the invention contains in fatty component a) fatty acids with a melting point in the range from 40 to 80, preferably in the range from 45 to 65 ° C. The fatty acids can be of natural and synthetic origin and are generally straight-chain and in particular saturated. Natural fatty acids are derived from triglycerides, for example from coconut oil, palm kernel oil, olive oil or also from animal fats such as beef tallow, fish oil or lard. Depending on their origin, the fatty acids derived therefrom are mixtures of different fatty acids and are also preferred if, after hydrogenation if necessary, they have a melting point in the range from 40 to 80, in particular in the range from 45 to 65 ° C.
Außer den bereits genannten Fettsäureglyceriden beziehungsweise Fettsäuren kann die Fettkomponente a) auch Fettalkohole enthalten. Für die erfin¬ dungsgemäßen Mittel bevorzugte Fettalkohole haben 10 bis 22 Kohlenstoff¬ atome im Molekül. Für die Herkunft der Fettalkohole gilt das gleiche wie oben für die Fettsäuren ausgeführt. Daß heißt, die Fettalkohole können ebenfalls synthetischen oder natürlichen Ursprungs sein und, gegebenen¬ falls nach Hydrierung, Gemische verschiedener Fettalkohole darstellen. Bevorzugt sind Fettalkohole mit 10 bis 22 Kohlenstoffatomen.In addition to the fatty acid glycerides or fatty acids already mentioned, the fat component a) can also contain fatty alcohols. Fatty alcohols preferred for the agents according to the invention have 10 to 22 carbon atoms in the molecule. The same applies to the origin of the fatty alcohols as stated above for the fatty acids. That means the fatty alcohols can likewise of synthetic or natural origin and, if appropriate after hydrogenation, represent mixtures of different fatty alcohols. Fatty alcohols having 10 to 22 carbon atoms are preferred.
Die für die Komponente b) geeigneten Fettalkohol-Alkoxylate basieren im allgemeinen auf den Fettalkoholen, wie sie auch für die- Fettkomponente a) geeignet sind. Pro Mol Fettalkohol enthalten sie 1 bis 15 Mol Ethylenoxid und/oder 1 bis 15 Mol Propylenoxid. Bevorzugt sind Fettalkohol-Alkoxylate, bei denen gleichzeitig Ethylenoxid und Propylenoxid an den Fettalkohol angelagert ist. Insbesondere enthalten geeignete Fettalkohol-Alkoxylate pro Mol Fettalkohol 2 bis 8 Mol Ethylenoxid und/oder Propylenoxid.The fatty alcohol alkoxylates suitable for component b) are generally based on the fatty alcohols, as are also suitable for the fatty component a). They contain 1 to 15 moles of ethylene oxide and / or 1 to 15 moles of propylene oxide per mole of fatty alcohol. Fatty alcohol alkoxylates in which ethylene oxide and propylene oxide are simultaneously attached to the fatty alcohol are preferred. In particular, suitable fatty alcohol alkoxylates contain 2 to 8 moles of ethylene oxide and / or propylene oxide per mole of fatty alcohol.
Außer Fettalkohol-Alkoxylate kann die Komponente b) Fettsäureester ein¬ wertiger Alkohole enthalten. Bevorzugte Fettsäureester einwertiger Alkohole enthalten insgesamt 15 bis 44 Kohlenstoffatome. Als einwertige" Alkoholkomponente kommen insbesondere Methylalkohol, Ethylalkohol n-Propylalkohol und iso-Propylalkohol in Frage. Für die Fettsäurekompo¬ nente der geeigneten Fettsäureester einwertiger Alkohole gilt das gleiche wie oben für die Fettsäuren bereits ausgeführt. Unter Fettsäureester ein¬ wertiger Alkohole werden im Rahmen der vorliegenden Erfindung auch unter¬ schiedlich zusammengesetzte Fettsäureester-Gemische verstanden. Hierzu gehören beispielsweise das aus den Blättern der brasilianischen Fächer¬ palme Copernica prunivera erhältliche Carnaubawachs, das aus den Blättern der Euphorbiaceae gewonnene CandeliIlawachs, Jojobaöl und natürliches oder synsthetisches Bienenwachs. Als synthetisches Bienenwachs kommt beispiels¬ weise ein Gemisch in Frage, das 40 Gew.-Teile eines Fettsäure ono- glycerids, dessen Säurekomponente ein 3 : 1-Gemisch aus HydroxyStearin¬ säure und gehärtetem Rizinusöl ist, das ferner 35 Gew.-Teile Palmitin- säurecetylester, 20 Gew.-Teile Mikrowachs, 10 Gew.-Teile Hydroxystearin- säure sowie weiteren Bestandteile in untergeordneten Mengen enthält. Der¬ artige natürliche Estergemische werden im Rahmen der vorliegenden Erfin¬ dung ebenfalls zu den Fettsäureestern einwertiger Alkohole gezählt.In addition to fatty alcohol alkoxylates, component b) may contain fatty acid esters of monohydric alcohols. Preferred fatty acid esters of monohydric alcohols contain a total of 15 to 44 carbon atoms. Monovalent "alcohol component in particular methyl alcohol, ethyl alcohol are n-propyl and iso-propyl alcohol in question. For the Fettsäurekompo¬ the appropriate fatty acid ester component of monovalent alcohols, the same applies as already explained above for the fatty acids. Under fatty acid ester of monohydric alcohols are within the scope of The present invention is also understood to mean mixtures of fatty acid esters of various compositions, for example carnauba wax obtainable from the leaves of the Brazilian fan palm Copernica prunivera, candeliol wax obtained from the leaves of Euphorbiaceae, jojoba oil and natural or synthetic beeswax ¬ a mixture in question, the 40 parts by weight of a fatty acid onoglyceride, the acid component of which is a 3: 1 mixture of hydroxystearic acid and hardened castor oil, and 35 parts by weight of palmitic acid, 20 Parts by weight of micro wax, 10 parts by weight of hydroxystearic acid and other constituents in minor amounts. Such natural ester mixtures are also counted among the fatty acid esters of monohydric alcohols in the context of the present invention.
Damit die Wirk.stoffgemische den bevorzugten Kristallisationsbeginn bei einer Temperatur von 40 °C oder höher haben, bestehen die Wirkstoffge- mische aus der Komponente a) und der Komponente b) im Gew.-Verhältnis von 3 : 1 bis 1 : 3, vorzugsweise im Gew.-Verhältnis von 2 : 1 bis 1 : 2. Erfindungsgemäße Mittel, bei denen die Wirkstoffgemische die Komponente a) und die Komponente b) im genannten Gew.-Verhältnis enthalten, sind bevor¬ zugt. Gelegentlich kann es zweckmäßig sein, den Kristallisationsbeginn durch Zusätze organischer Lösungsmittel zu modifizieren. Insbesondere ge¬ eignet ist hierfür der Zusatz einer wirksamen Menge von Glycerin, die im allgemeinen 1 bis 15 Gew.-%, bezogen auf die Wirkstoffgemische, ausmacht.So that the effect . Mixtures have the preferred start of crystallization at a temperature of 40 ° C or higher, the active ingredient mixtures consist of component a) and component b) in a weight ratio of 3: 1 to 1: 3, preferably in a weight ratio of 2: 1 to 1: 2. Agents according to the invention in which the active compound mixtures contain component a) and component b) in the weight ratio mentioned are preferred moves. Occasionally, it may be appropriate to modify the start of crystallization by adding organic solvents. The addition of an effective amount of glycerol, which generally makes up 1 to 15% by weight, based on the active ingredient mixtures, is particularly suitable for this purpose.
Obgleich es grundsätzlich möglich ist, daß die als Träger für das Wirk- stoffgemisch eingesetzten flexiblen Flächengebilde eine für eine einmalige Anwendung oder auch für eine mehrmalige Anwendung ausreichende Menge der Wirkstoffsgemische enthalten, ist es bevorzugt, daß die Mittel eine für eine einmalige Anwendung ausreichende Menge an der Komponente a) + b) ent¬ halten. Vorzugsweise ist dies eine Menge von 1 bis 5 g, die auf das flexible Flächengebilde einseitig oder beidseitig appliziert wird.Although it is fundamentally possible for the flexible sheet materials used as carriers for the active substance mixture to contain an amount of the active substance mixtures which is sufficient for a single application or for repeated use, it is preferred that the agents have an amount which is sufficient for a single application contain components a) + b). This is preferably an amount of 1 to 5 g, which is applied to the flexible fabric on one or both sides.
Für die Applikation der Wirkstoffgemische auf das flexible Flächengebilde werden die Wirkstoffgemische durch Erwärmen verflüssigt. Besonders geeig¬ nete Wirkstoffgemische haben bei 60 °C eine Viskosität von 5 bis 100 mPas; sie sind daher bevorzugt.For the application of the active ingredient mixtures to the flexible fabric, the active ingredient mixtures are liquefied by heating. Particularly suitable mixtures of active ingredients have a viscosity of 5 to 100 mPas at 60 ° C .; they are therefore preferred.
Dadurch, daß die Bestandteile der Wirkstoffgemische der erfindungsgemäßen Mittel aufgrund ihrer Herkunft aus natürlichen und nachwachsenden Roh¬ stoffen keine nennenswerten Mengen an brennbaren Flüssigkeiten enthalten, ist der Flammpunkt der Wirkstoffgemische deutlich höher als der im allge¬ meinen für die bekannten Mittel zur Behandlung gewaschener Wäsche im Wäschetrockner verwendeten Wirkstoffgemische. Dies ist ein weiterer Vor¬ teil der erfindungsgemäßen Mittel. Erfindungsgemäße Mittel, deren Wirk¬ stoffgemische einen Flammpunkt von mehr als 55 °C, vorzugsweise von mehr als 100 °C haben, sind daher besonders bevorzugt. Ein derartig hoher Flammpunkt wirkt sich besonders günstig bei der Herstellung der erfin¬ dungsgemäßen Mittel aus, bei der die Wirkstoffgemische bei erhöhter Temperatur auf das flexible Flächengebilde aufgetragen werden.Because the constituents of the active substance mixtures of the compositions according to the invention, because of their origin from natural and renewable raw materials, do not contain any noteworthy amounts of flammable liquids, the flash point of the active substance mixtures is significantly higher than that for the known compositions for the treatment of washed laundry in general Dryer mixtures used active ingredients. This is a further advantage of the agents according to the invention. Agents according to the invention, the active ingredient mixtures of which have a flash point of more than 55 ° C., preferably more than 100 ° C., are therefore particularly preferred. Such a high flash point has a particularly favorable effect on the production of the agents according to the invention, in which the active substance mixtures are applied to the flexible fabric at elevated temperature.
Das flexible Flächengebilde der erfindungsgemäßen Mittel kann ein faseri¬ ges Flächengebilde sein und dementsprechend ein gewebtes, ein gewirktes textiles Material oder auch ein Faservlies sein. Auch schäum- oder schwa martige Materialien natürlichen oder synthetischen Ursprungs, wie beispielsweise geschäumte synthetische Polymere, die vorzugsweise in Plattenform vorliegen, sind als flexible Flächengebilde geeignet. Die textilen Flächengebilde haben in der Regel eine niedrigere Adsorptions¬ kapazität als die schäum- oder schwammartigen Materialien. Die niedrigere Adsorptionskapazität ist gewöhnlich verbunden mit einer hohen Abgaberate der Wirkstoffsgemische, wohingegen die schäum- oder schwammartigen Materialien zwar mehr Wirkstoffgemisch aufnehmen können, dieses aber im allgemeinen bei der Anwendung im Wäschetrockner weniger vollständig wieder abgeben. Bewährt haben sich vor allem die textilen flexiblen Flächen¬ gebilde, und hiervon insbesondere die Faservliese. Diese haben im Ver¬ gleich zu den schäum- oder schwammartigen Materialien eine niedrige bis mittlere Adsorptionskapazität und sind für die erfindungsgemäßen Mittel bevorzugt. Besonders bevorzugt als Träger für die Wirkstoffgemische sind flexible Flächengebilde, die ein Vlies aus synthetischen und natürlichen Fasermaterial en darstellen.The flexible surface structure of the agents according to the invention can be a fibrous surface structure and accordingly a woven, a knitted one textile material or a non-woven fabric. Foam or sponge-like materials of natural or synthetic origin, such as foamed synthetic polymers, which are preferably in sheet form, are also suitable as flexible fabrics. The textile fabrics generally have a lower adsorption capacity than the foam or sponge-like materials. The lower adsorption capacity is usually associated with a high rate of release of the active ingredient mixtures, whereas the foam or sponge-like materials can absorb more of the active ingredient mixture, but generally release it less completely when used in the tumble dryer. Above all, the flexible textile fabrics, and in particular the non-woven fabrics, have proven successful. Compared to the foam or sponge-like materials, these have a low to medium adsorption capacity and are preferred for the agents according to the invention. Particularly preferred as a carrier for the active ingredient mixtures are flexible fabrics which are a nonwoven made of synthetic and natural fiber materials.
Obwohl die erfindungsgemäßen Mittel in ihren Wirkstoffgemisehen keinerlei salzartige Bestandteile, wie beispielsweise quartäre Ammoniumsalze, ent¬ halten, weisen die mit den erfindungsgemäßen Mittel behandelten Textilien nach der Behandlung im Wäschetrockner, die bei Temperaturen von etwa 50 bis 80 °C stattfindet, überraschend gute antielektrostatische Eigen¬ schaften auf. Außerdem überzeugen die erfindungsgemäßen Mittel durch die Summe der vorhandenen wünschenswerten Eigenschaften. Sie lassen sich leicht herstellen, fühlen sich nach der Herstellung nicht unangenehm an, haben die Eigenschaft, die Wirkstoffgemische bei der Anwendung im Wäsche¬ trockner nahezu vollständig abzugeben und auf die zu behandelnden Textilien zu übertragen, sie verleihen den zu behandelnden Textilien einen angenehmen weichen und vollen Griff und ausgezeichnete antielektro¬ statische Eigenschaften. Da die Wirkstoffgemische außerdem frei von quartären Ammoniumverbindungen sind, ist die Belastung der Umwelt durch die mit dem Waschwasser der auf die Behandlung im Wäschetrockner folgenden Wäsche in die Kanalisation gelangenden Wirkstoffe äußert gering. Ein weiterer Vorteil der erfindungsgemäßen Mittel ist die Tatsache, daß die in den Wirkstoffgemisehen vorhandenen Komponenten aus natürlichen und nach¬ wachsenden Rohstoffen hergestellt werden.Although the compositions according to the invention do not contain any salt-like constituents, such as quaternary ammonium salts, in their active ingredient mixtures, the textiles treated with the compositions according to the invention have surprisingly good antielectrostatic properties after treatment in a tumble dryer, which takes place at temperatures of about 50 to 80 ° C. ¬ shafts. In addition, the agents according to the invention convince through the sum of the desirable properties present. They are easy to manufacture, do not feel uncomfortable after manufacture, have the property of releasing the active substance mixtures almost completely when used in the tumble dryer and transferring them to the textiles to be treated, and they give the textiles to be treated a pleasantly soft and full grip and excellent anti-electrostatic properties. Since the active ingredient mixtures are also free of quaternary ammonium compounds, the environmental impact from the active ingredients which enter the sewer system with the washing water of the laundry following treatment in the tumble dryer is extremely low. Another advantage of the agents according to the invention is the fact that the in the components present in the active ingredient mixture are produced from natural and renewable raw materials.
Außer den genannten Bestandteilen können die Wirkstoffgemische zusätzlich in Mitteln zur Behandlung gewaschener Wäsche im Wäschetrockner übliche Hilfs- und Zusatzstoffe enthalten. Dies sind beispielsweise Duftstoffe, Farbstoffe, Schwermetallkomplexbildner, Tonmaterialien oder feinteilige Kieselsäure. In addition to the constituents mentioned, the active substance mixtures can additionally contain customary auxiliaries and additives in agents for treating washed laundry in a tumble dryer. These are, for example, fragrances, dyes, heavy metal complexing agents, clay materials or finely divided silica.
B e i s p e l eB e i s p e l e
Auf ein aus Polyester- und Cellulosefasern bestehendes Wirrfaservlies "Keybak 02", der Firma Chicopee, Niederlande, der Größe 14 cm x 25 cm wurden 3 g eines Wirkstoffgemischs der beiden folgenden Zusammensetzungen A und B gleichmäßig aufgetragen.3 g of a mixture of active ingredients of the two following compositions A and B were uniformly applied to a "Keybak 02" non-woven fabric "Keybak 02" from Chicopee, the Netherlands, consisting of polyester and cellulose fibers.
Der Kristallisationsbeginn für Gemisch A lag bei 42 °C, der für Gemisch B bei 46 °C. Für handelsübliches 75 Gew.-%iges Distearyldimethylammonium- chlorid (DSDMAC) mit der gleichen Menge Parfümöl lag der Kristallisations¬ beginn bei 27 °C.The start of crystallization for mixture A was 42 ° C, that for mixture B at 46 ° C. For commercially available 75% by weight distearyldimethylammonium chloride (DSDMAC) with the same amount of perfume oil, the start of crystallization was 27 ° C.
Der Flammpunkt von Mischung A lag bei 166 °C, bei Mischung B bei 156 °C, wohingegen er bei dem DSDMAC-Gemisch bei 28 °C lag. Dementsprechend ist das DSDMAC-Gemisch als Gefahrgut zu behandeln, die Wirkstoffgemische A und B der erfingungsgemäßen Mittel hingegen nicht. Damit behandelte Textilien hatten in allen Fällen einen etwa gleich guten Griff. Die antielektrostatischen Eigenschaften, gemessen als Halbwertszeit des Abbaus einer aufgebrachten elektrischen Ladung, betrugen 7,6 Sekunden (A) beziehungsweise 10,6 Sekunden (B) und 36 Sekunden DSDMAC.The flash point of mixture A was 166 ° C, for mixture B 156 ° C, whereas for the DSDMAC mixture it was 28 ° C. Accordingly, the DSDMAC mixture is to be treated as dangerous goods, but the active substance mixtures A and B of the agents according to the invention are not. Textiles treated with this had an approximately equally good grip in all cases. The anti-electrostatic properties, measured as the half-life of the dissipation of an applied electrical charge, were 7.6 seconds (A) and 10.6 seconds (B) and 36 seconds DSDMAC.
In allen Fällen war die Wirkstoffabgabe praktisch vollständig (über 96%ige Abgaberate).In all cases, drug delivery was virtually complete (over 96% delivery rate).
Die behandelten Textilien wiesen trotz der Verwendung eines Träger¬ materials mit der verhältnismäßig geringer Adsorptionskapazität von ca. 6, gemessen nach dem in US-Federal Specifications UU-T-595 b beschriebenen und gemäß DE-A 27 00 512 modifizierten Verfahren, keine Fleckenbildung auf.Despite the use of a carrier material with the relatively low adsorption capacity of approx. 6, measured according to the method described in US Federal Specifications UU-T-595 b and modified according to DE-A 27 00 512, the treated textiles showed no staining .
Das toxikologische, ökologische und ökotoxikologische Verhalten der Wirkr Stoffgemische A und B war in jeder Hinsicht besser als das von DSDMAC. The toxicological, ecological and ecotoxicological behavior of the active substance mixtures A and B was better than that of DSDMAC in every respect.

Claims

P a t e n t a n s p r ü c h e Patent claims
1. Mittel zum Behandeln gewaschener Wäsche in einem Wäschetrockner beste¬ hend aus einem mit Wirkstoffgemisehen zur Wäschebehandlung beladenen flexiblen Flächengebilde, wobei die Wirkstoffgemisehe eine Fett¬ komponente enthalten, dadurch gekennzeichnet, daß die Mono-, Di- oder Trifettsäureglyceride und/oder Fettsäuren und/oder Fettalkohole um¬ fassende Fettkomponente a) im Gemisch mit b) Fettalkohol-Alkoxylaten und/ oder Fettsäureestern einwertiger Alkohole vorliegt.1. Means for treating washed laundry in a tumble dryer consisting of a flexible fabric loaded with active ingredients for laundry treatment, the active ingredients containing a fat component, characterized in that the mono-, di- or trifatty acid glycerides and / or fatty acids and / / or fatty component a) comprising fatty alcohols in a mixture with b) fatty alcohol alkoxylates and / or fatty acid esters of monohydric alcohols.
2. Mittel nach Anspruch 1, dadurch gekennzeichnet, daß die Wirkstoffge¬ mische einen Kristallisationsbeginn bei einer Temperatur von 40 °C oder höher haben.2. Composition according to claim 1, characterized in that the active ingredient mixtures have a start of crystallization at a temperature of 40 ° C or higher.
3. Mittel nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß die Fett¬ komponente a) Mono- und Di-Fettsäureglycerid, vorzugsweise Mono-Fett- säureglyceride enthält.3. Composition according to claim 1 or 2, characterized in that the Fett¬ component a) contains mono- and di-fatty acid glyceride, preferably mono-fatty acid glycerides.
4. Mittel nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß die Fettkomponente a) Fettsäuren mit einem Schmelzpunkt im Bereich von 40 - 80 °C, vorzugsweise von 45 - 65 °C enthält.4. Composition according to one of claims 1 to 3, characterized in that the fat component a) contains fatty acids with a melting point in the range of 40-80 ° C, preferably 45-65 ° C.
5. Mittel nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, daß die Fettkomponente a) Fettalkohole mit 10 bis 22 Kohlenstoffatomen enthält.5. Composition according to one of claims 1 to 4, characterized in that the fat component a) contains fatty alcohols with 10 to 22 carbon atoms.
6. Mittel nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, daß die Komponente b) Fettalkohol, an den Ethylenoxid und Propylenoxid angelagert ist, enthält.6. Composition according to one of claims 1 to 5, characterized in that component b) contains fatty alcohol to which ethylene oxide and propylene oxide is attached.
7. Mittel nach einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, daß die Komponente b) Fettsäureester einwertiger Alkohole mit 15 bis 44 Kohlenstoffatomen enthält. 7. Composition according to one of claims 1 to 6, characterized in that component b) contains fatty acid esters of monohydric alcohols with 15 to 44 carbon atoms.
8. Mittel nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß es die Komponente a) und die Komponente b) im Verhältnis 3 : 1 bis 1 : 3, vorzugsweise im Verhältnis 2 : 1 bis 1 : 2 enthält.8. Composition according to one of claims 1 to 7, characterized in that it contains component a) and component b) in a ratio of 3: 1 to 1: 3, preferably in a ratio of 2: 1 to 1: 2.
9. Mittel nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß es eine für eine einmalige Anwendung ausreichende Menge der Komponen¬ ten a) + b), vorzugsweise eine Menge von 1 bis 5 g enthält.9. Composition according to one of claims 1 to 8, characterized in that it contains a sufficient amount for a single use of the components a) + b), preferably an amount of 1 to 5 g.
10. Mittel nach einem der Ansprüche 1 bis 9, dadurch gekennzeichnet, daß die Wirkstoffgemische eine Viskosität von 5 bis 100 mPas bei 60 °C haben.10. Agent according to one of claims 1 to 9, characterized in that the active substance mixtures have a viscosity of 5 to 100 mPas at 60 ° C.
il. Mittel nach einem der Ansprüche 1 bis 10, dadurch gekennzeichnet, daß die Wirkstoffgemische einen Flammpunkt von mehr als 55 °C, vorzugsr weise von mehr als 100 °C haben.il. Agent according to one of claims 1 to 10, characterized in that the active substance mixtures have a flash point of more than 55 ° C, preferably of more than 100 ° C.
12. Mittel nach einem der Ansprüche 1 bis 11, dadurch gekennzeichnet, daß das als Träger für die Wirkstoffgemische dienende flexible Flächenge¬ bilde ein Vlies aus synthetischen und natürlichen Fasermaterialien ist. 12. Composition according to one of claims 1 to 11, characterized in that the serving as a carrier for the active substance mixtures flexible surface structure is a nonwoven made of synthetic and natural fiber materials.
EP92916357A 1991-08-03 1992-07-27 Agent for treating washed clothes in a clothes drier Withdrawn EP0596968A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4125847 1991-08-03
DE4125847A DE4125847A1 (en) 1991-08-03 1991-08-03 AGENT FOR TREATING WASHED LAUNDRY IN A LAUNDRY DRYER
PCT/EP1992/001701 WO1993003132A1 (en) 1991-08-03 1992-07-27 Agent for treating washed clothes in a clothes drier

Publications (1)

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EP0596968A1 true EP0596968A1 (en) 1994-05-18

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Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4224067A1 (en) * 1992-07-21 1994-01-27 Henkel Kgaa Tumbler aids
ATE207106T1 (en) * 1996-01-19 2001-11-15 Unilever Nv NON-CATIONIC SYSTEMS FOR FABRIC DRYER SHEETS
FR2745013B1 (en) * 1996-02-19 1998-04-03 James River COMPOSITION FOR SOFTENING LOTION, USE OF THE LOTION FOR THE TREATMENT OF FIBERS AND ABSORBENT PAPER PRODUCT THEREOF
EP0831147A3 (en) * 1996-09-19 1998-12-16 Unilever Plc Non-cationic systems for dryer sheets
US5919750A (en) * 1997-07-24 1999-07-06 Akzo Nobel Nv Fabric softener composition
EP1930500A1 (en) * 2006-12-08 2008-06-11 Cognis IP Management GmbH Emulsions for the softening of textiles and paper

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3442692A (en) * 1965-08-13 1969-05-06 Conrad J Gaiser Method of conditioning fabrics
US3686025A (en) * 1968-12-30 1972-08-22 Procter & Gamble Textile softening agents impregnated into absorbent materials
US4000340A (en) * 1973-10-29 1976-12-28 The Procter & Gamble Company Clothes dryer additive containing crisping agents
US4209549A (en) * 1974-02-08 1980-06-24 The Procter & Gamble Company Process for treating fabrics with fabric treatment compositions
US4022938A (en) * 1974-04-16 1977-05-10 The Procter & Gamble Company Fabric treatment compositions
AU510901B2 (en) * 1976-01-09 1980-07-17 Procter & Gamble Company, The Fabric softening method and device
DE3003249A1 (en) * 1980-01-30 1981-08-06 Henkel KGaA, 4000 Düsseldorf AGENT FOR TREATING WASHED LAUNDRY IN A LAUNDRY DRYER
ZA914152B (en) * 1990-06-01 1993-01-27 Unilever Plc Liquid fabric conditioner and dryer sheet fabric conditioner containing fabric softener,aminosilicone and bronsted acid compatibiliser
US5145595A (en) * 1990-10-03 1992-09-08 Vista Chemical Company Anti-static fabric softening article for use in an automatic clothes dryer

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9303132A1 *

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DE4125847A1 (en) 1993-02-04
US5399271A (en) 1995-03-21

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