WO2012130701A1 - Wasch- oder reinigungsmittel mit modifizierten riechstoffen - Google Patents

Wasch- oder reinigungsmittel mit modifizierten riechstoffen Download PDF

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Publication number
WO2012130701A1
WO2012130701A1 PCT/EP2012/055045 EP2012055045W WO2012130701A1 WO 2012130701 A1 WO2012130701 A1 WO 2012130701A1 EP 2012055045 W EP2012055045 W EP 2012055045W WO 2012130701 A1 WO2012130701 A1 WO 2012130701A1
Authority
WO
WIPO (PCT)
Prior art keywords
fragrances
weight
oil
metal oxides
composition according
Prior art date
Application number
PCT/EP2012/055045
Other languages
German (de)
English (en)
French (fr)
Inventor
Georg Meine
Andrea Eutebach
Frank Sonnenschein
Ralf Bunn
Sebastian GABRIEL
Hubert Smyrek
Manuela Materne
Frank Rittler
Original Assignee
Henkel Ag & 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 & Co. Kgaa filed Critical Henkel Ag & Co. Kgaa
Priority to EP12710720.9A priority Critical patent/EP2691504B1/de
Priority to ES12710720.9T priority patent/ES2609630T3/es
Publication of WO2012130701A1 publication Critical patent/WO2012130701A1/de
Priority to US14/038,952 priority patent/US8815786B2/en

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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/1213Oxides or hydroxides, e.g. Al2O3, TiO2, CaO or Ca(OH)2
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • C11D3/502Protected perfumes
    • C11D3/505Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50Perfumes
    • C11D3/502Protected perfumes
    • C11D3/507Compounds releasing perfumes by thermal or chemical activation

Definitions

  • WO 2010/076803 A2 describes a topical multicomponent system in which at least one component comprises an active substance which is coated with a metal oxide. Detergents or cleaning agents are not described.
  • a solution or dispersion of the starting materials is preferably first prepared, and this mixture is advantageously stirred for a period of at least 1 minute at room temperature (21 ° C).
  • thermal energy may also be supplied, e.g. by heating to 60 ° C.
  • the particle size of the metal oxides used is basically freely selectable. However, it is preferred that the metal oxides particle sizes ⁇ 1000 ⁇ , advantageously ⁇ 500 ⁇ , in a further advantageous manner ⁇ 100 ⁇ , preferably ⁇ 1 ⁇ , in particular ⁇ 0.1 ⁇ . A possible lower limit of the particle size may e.g. at 1 nm or 10 nm.
  • the washing or cleaning agent according to the invention makes it possible to produce a fragrance on the substrates treated therewith.
  • the invention goes hand in hand with some further advantages.
  • a significant advantage is that the invention allows a fragrant effect by Wederbefeuchten.
  • objects treated with the washing or cleaning agent according to the invention e.g. Textiles, after which they surprisingly exude a particularly intense fragrance when they are moistened again.
  • This effect is beneficial for many processes of daily life.
  • a towel washed with the detergent of the invention unfolds on drying e.g. of crockery or the human body, by the absorbed moisture a fragrance effect.
  • appropriate underwear e.g. Undershirt, by the body moisture a renewed fragrance effect are triggered.
  • This effect ie a re-flow of fragrance after the Wederbetwoeren, does not occur in the application of ordinary detergents or cleaning agents, i. It is usually not expected that a towel exudes fragrance as soon as it is moistened again.
  • Another advantage lies in the improvement of the absorption of fragrances from aqueous, preferably surfactant-containing solutions on the treated objects, in particular textiles. This not only affects the fragrances introduced via the reaction products according to the invention, but also benefits the other fragrances which are not introduced into the system via the reaction products according to the invention. This allows for improved efficiency in fragrance use.
  • Another advantage lies in the improved fixation of fragrances on soft and hard surfaces, such as textiles, skin and hair or hard surfaces. With improved fixation here is meant an improved, so strong adhesion of the already scented on the objects fragrances.
  • Bad-odor components are volatile compounds with kakosmophoren groups, eg. As amine derivatives and sulfur derivatives.
  • the present invention can afford not only a targeted release of fragrances, but also a recording and thus reduction of malodors.
  • the amount of metal oxide present preferably introduced via the reaction product according to the invention into the washing or cleaning agent, is 0.00001 to 10% by weight, preferably 0.01 to 1% by weight, based on the total washing or cleaning agent is a preferred embodiment of the invention.
  • the washing or cleaning agent according to the invention contains 0.0001 to 95 wt .-%, preferably 0.01 to 40 wt .-% surfactants.
  • a particularly preferred washing or cleaning agent according to the invention contains
  • Another object of the invention is a process for the preparation of a detergent or cleaning agent, wherein a reaction product of fragrances with metal produces oxides and this reaction product combined with the detergent or cleaning agent matrix.
  • a reaction product of fragrances with metal produces oxides and this reaction product combined with the detergent or cleaning agent matrix.
  • washing or cleaning agent in the context of the invention also includes the aftertreatment agents. These include, in particular, the fabric softeners, the hygiene rinse and the dryer sheets (so-called dryer sheets), but also the textile fresheners and ironing water.
  • the corresponding agents preferably contain the usual ingredients for the product category in question.
  • a hygiene rinse usually contains active ingredients that, depending on the individual case, can kill a wide range of organisms from viruses, bacteria, fungi.
  • active substances such as, for example, alkylbenzyldimethylammonium chloride, are known per se to the person skilled in the art.
  • fabric softeners contain softening active ingredients, generally cationic surfactants, preferably esterquats, ie quaternary ammonium compounds having two hydrophobic radicals, each containing an ester group as a so-called predetermined breaking point for easier biodegradation.
  • textile fresheners care products for spraying textiles in the household in order to absorb volatile, unpleasant-smelling molecules and to mask them with pleasant scents are referred to as textile fresheners.
  • textile fresheners For absorption, in conventional textile Shear eg cyclodextrins used. Drying cloths are intended for use in the tumble dryer. These are wipes on which certain active substances are applied so that the textiles are less wrinkled and less easily electrostatically charged.
  • Detergents or cleaning agents according to the invention preferably comprise, in addition to the reaction product according to the invention, at least one, preferably several, active components, in particular washing, care and / or cleaning active components, advantageously selected from the group comprising anionic surfactants, cationic surfactants, amphoteric surfactants, nonionic surfactants, acidifiers , Alkalizing agents, anti-wrinkling compounds, antibacterials, antioxidants, anti redeposition agents, antistatic agents, builders, bleaches, bleach activators, bleach stabilizers, bleach catalysts, ironing aids, fragrances, anti-shrinkage agents, electrolytes, enzymes, colorants, dyes, dye transfer inhibitors, fluorescers , Fungicides, germicides, odor-complexing substances, hydrotropes, rinse aids, complexing agents, preservatives, corrosion inhibitors, optical brighteners, pearlescers, pH adjusters, phobizers and impregnating agents, polymers, swelling and sliding agents, foam inhibitors,
  • the derivatives of the fatty alcohols although also their branched-chain isomers, in particular so-called oxo alcohols, can be used for the preparation of usable alkoxylates.
  • Useful are accordingly the alkoxylates, in particular the ethoxylates, primary alcohols with linear, in particular dodecyl, tetradecyl, hexadecyl or octadecyl radicals and mixtures thereof.
  • suitable alkoxylation products of alkylamines, vicinal diols and carboxylic acid amides which correspond to the said alcohols with respect to the alkyl part, usable.
  • the ethylene oxide and / or propylene oxide insertion products of fatty acid alkyl esters and fatty acid polyhydroxyamides are also suitable.
  • alkoxylates are those which are obtained by ethoxylation of branched primary alcohols, in particular by ethoxylation of corresponding branched primary alcohols having 1 to 36 carbon atoms and an average of 0.7 to 3.0 branches per molecule, which branches include methyl and ethyl branches.
  • Such alkoxylates are described in US Pat. No. 7,871,973 B1.
  • Nonionic surfactant is preferably present in detergents or cleaners according to the invention in amounts of from 0.1% by weight to 30% by weight, in particular from 1% by weight to 25% by weight, based on the weight entire washing or cleaning agent.
  • Cationic surfactants can also be present optionally in the detergents or cleaners according to the invention, in particular in the laundry aftertreatment compositions according to the invention.
  • cationic surfactants are quaternary ammonium compounds having preferably one or in particular two hydrophobic alkyl radicals.
  • Particularly preferred are esterquats, ie quaternary ammonium compounds having two hydrophobic radicals, each containing an ester group as a so-called predetermined breaking point for easier biodegradation.
  • the water-soluble organic builder substances include polycarboxylic acids, in particular citric acid and sugar acids, 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 also polymeric (poly) -carboxylic acids, polymeric acrylic acids, methacrylic acids, maleic acids and mixed polymers thereof, which may also contain polymerized small amounts of polymerizable substances without carboxylic acid functionality.
  • polycarboxylic acids in particular citric acid and sugar acids
  • monomeric and polymeric aminopolycarboxylic acids in particular methylglycinediacetic acid, nitrilotriace
  • Suitable, albeit less preferred, compounds of this class are copolymers of acrylic acid or methacrylic acid with vinyl ethers, such as vinylmethyl ethers, vinyl esters, ethylene, propylene and styrene, in which the proportion of the acid is at least 50% by weight.
  • the optionally usable foam inhibitors include, for example, organopolysiloxanes and mixtures thereof with microfine, optionally silanized silica and paraffin waxes and mixtures thereof with silanated silica or bis-fatty acid alkylenediamides.
  • mixtures of different foam inhibitors can be used, for example those of silicones, paraffins or waxes.
  • the optional foam inhibitors, in particular silicone and / or paraffin-containing foam inhibitors are bound to a granular, water-soluble or dispersible carrier substance.
  • mixtures of paraffin waxes and bistearylethylenediamides are preferred.
  • the optionally applicable graying inhibitors have the ability to keep 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 polyamides containing acidic groups are suitable for this purpose.
  • starch derivatives can be used, for example aldehyde starches.
  • alcohols and / or organic solvents can be used with up to 50%.
  • a liquid, hydrophobic compound selected from limonene, dioctyl ether, lauric acid hexyl ester, decamethylcyclopentasiloxane, C.sub.1-isoparaffin and mixtures thereof, preferably in combination with fatty acid soap and / or unneutralized fatty acid.
  • anionic surfactants such as preferably alkylbenzenesulfonate, alkylsulfate, e.g. in amounts of preferably 5-30% by weight
PCT/EP2012/055045 2011-03-29 2012-03-22 Wasch- oder reinigungsmittel mit modifizierten riechstoffen WO2012130701A1 (de)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP12710720.9A EP2691504B1 (de) 2011-03-29 2012-03-22 Wasch- oder reinigungsmittel mit modifizierten riechstoffen
ES12710720.9T ES2609630T3 (es) 2011-03-29 2012-03-22 Agentes de lavado o de limpieza con fragancias modificadas
US14/038,952 US8815786B2 (en) 2011-03-29 2013-09-27 Detergents or cleaning agents containing reaction products of odorants with metal oxides

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102011006315.3 2011-03-29
DE102011006315A DE102011006315A1 (de) 2011-03-29 2011-03-29 Wasch- oder Reinigungsmittel mit modifizierten Riechstoffen

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US14/038,952 Continuation US8815786B2 (en) 2011-03-29 2013-09-27 Detergents or cleaning agents containing reaction products of odorants with metal oxides

Publications (1)

Publication Number Publication Date
WO2012130701A1 true WO2012130701A1 (de) 2012-10-04

Family

ID=45888213

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2012/055045 WO2012130701A1 (de) 2011-03-29 2012-03-22 Wasch- oder reinigungsmittel mit modifizierten riechstoffen

Country Status (5)

Country Link
US (1) US8815786B2 (deFl)
EP (1) EP2691504B1 (deFl)
DE (1) DE102011006315A1 (deFl)
ES (1) ES2609630T3 (deFl)
WO (1) WO2012130701A1 (deFl)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014162311A1 (en) * 2013-04-01 2014-10-09 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. Adjustable sol-gel-based capsules comprising fragrances and aromas, and uses thereof
US9953588B1 (en) * 2014-03-25 2018-04-24 E Ink Corporation Nano-particle based variable transmission devices

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109414020A (zh) 2016-05-12 2019-03-01 应用银股份有限公司 将金属离子分配到洗涤系统中的制品和方法
CN110113946A (zh) 2016-10-31 2019-08-09 应用银股份有限公司 向分批式洗衣机和烘干机中分配金属离子

Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1270040A (en) * 1967-01-27 1972-04-12 Unilever Ltd Liquid detergent compositions
GB1505493A (en) * 1974-03-07 1978-03-30 Unilever Ltd Preparation of detergent bars
EP0536942A2 (en) * 1991-10-02 1993-04-14 Unilever Plc Perfume particles
WO1997047720A2 (en) * 1996-06-11 1997-12-18 The Procter & Gamble Company Process for producing a particulate laundry additive for perfume delivery having improved physical properties
DE19841147A1 (de) 1998-09-09 2000-03-16 Henkel Kgaa Kiselsäureester
DE10212121A1 (de) 2002-03-15 2003-09-25 Bayer Ag Verfahren zur Herstellung von nano-Zinkoxid-Dispersionen stabilisiert durch hydroxylgruppenhaltige anorganische Polymere
JP2004180979A (ja) 2002-12-04 2004-07-02 Ogawa & Co Ltd 抗菌消臭剤組成物
DE10337198A1 (de) 2003-08-13 2005-03-17 Degussa Ag Träger auf Basis von Granulaten, die aus pyrogen hergestelltem Siliciumdioxiden hergestellt sind
DE102006003092A1 (de) 2006-01-20 2007-07-26 Henkel Kgaa 1-Aza-3,7-dioxabicyclo[3.3.0]octan-Verbindungen und ihre Verwendung als Pro-Fragrances
WO2008077239A1 (en) 2006-12-22 2008-07-03 Sidense Corp. A program lock circuit for a mask programmable anti-fuse memory array
WO2008112826A1 (en) 2007-03-12 2008-09-18 Board Of Regents, The University Of Texas System Method and process for the production of multi-coated recognitive and releasing systems
US20090035365A1 (en) * 2007-07-30 2009-02-05 Lewis Michael Popplewell Density Controlled Capsule Particles and Methods of Making the Same
WO2009103651A2 (en) 2008-02-21 2009-08-27 Basf Se Preparation of cationic nanoparticles and personal care compositions comprising said nanoparticles
DE102008031212A1 (de) 2008-07-03 2010-01-07 Henkel Ag & Co. Kgaa Wasch- und Reinigungsmitteladditiv in Partikelform
DE102008052678A1 (de) 2008-10-22 2010-04-29 Henkel Ag & Co. Kgaa Polyoxyalkylenmonoamin modifizierte mehrschichtige Nanopartikel
WO2010076803A2 (en) 2009-01-05 2010-07-08 Sol-Gel Technologies Ltd. Topical systems and kits
US7871973B1 (en) 1996-11-26 2011-01-18 Shell Oil Company Highly branched primary alcohol compositions, and biodegradable detergents made therefrom

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6558710B1 (en) * 1999-06-14 2003-05-06 Helen Rebecca Godfrey Topical zinc compositions and methods of use
US20050191257A1 (en) * 2004-02-27 2005-09-01 John Brahms Dry deodorant containing a sesquiterpene alcohol and zinc oxide
US7833960B2 (en) * 2006-12-15 2010-11-16 International Flavors & Fragrances Inc. Encapsulated active material containing nanoscaled material
WO2008108756A1 (en) * 2007-03-05 2008-09-12 Grune Guerry L Sunscreen compositions

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1270040A (en) * 1967-01-27 1972-04-12 Unilever Ltd Liquid detergent compositions
GB1505493A (en) * 1974-03-07 1978-03-30 Unilever Ltd Preparation of detergent bars
EP0536942A2 (en) * 1991-10-02 1993-04-14 Unilever Plc Perfume particles
WO1997047720A2 (en) * 1996-06-11 1997-12-18 The Procter & Gamble Company Process for producing a particulate laundry additive for perfume delivery having improved physical properties
US7871973B1 (en) 1996-11-26 2011-01-18 Shell Oil Company Highly branched primary alcohol compositions, and biodegradable detergents made therefrom
DE19841147A1 (de) 1998-09-09 2000-03-16 Henkel Kgaa Kiselsäureester
DE10212121A1 (de) 2002-03-15 2003-09-25 Bayer Ag Verfahren zur Herstellung von nano-Zinkoxid-Dispersionen stabilisiert durch hydroxylgruppenhaltige anorganische Polymere
JP2004180979A (ja) 2002-12-04 2004-07-02 Ogawa & Co Ltd 抗菌消臭剤組成物
DE10337198A1 (de) 2003-08-13 2005-03-17 Degussa Ag Träger auf Basis von Granulaten, die aus pyrogen hergestelltem Siliciumdioxiden hergestellt sind
DE102006003092A1 (de) 2006-01-20 2007-07-26 Henkel Kgaa 1-Aza-3,7-dioxabicyclo[3.3.0]octan-Verbindungen und ihre Verwendung als Pro-Fragrances
WO2008077239A1 (en) 2006-12-22 2008-07-03 Sidense Corp. A program lock circuit for a mask programmable anti-fuse memory array
WO2008112826A1 (en) 2007-03-12 2008-09-18 Board Of Regents, The University Of Texas System Method and process for the production of multi-coated recognitive and releasing systems
US20090035365A1 (en) * 2007-07-30 2009-02-05 Lewis Michael Popplewell Density Controlled Capsule Particles and Methods of Making the Same
WO2009103651A2 (en) 2008-02-21 2009-08-27 Basf Se Preparation of cationic nanoparticles and personal care compositions comprising said nanoparticles
DE102008031212A1 (de) 2008-07-03 2010-01-07 Henkel Ag & Co. Kgaa Wasch- und Reinigungsmitteladditiv in Partikelform
DE102008052678A1 (de) 2008-10-22 2010-04-29 Henkel Ag & Co. Kgaa Polyoxyalkylenmonoamin modifizierte mehrschichtige Nanopartikel
WO2010076803A2 (en) 2009-01-05 2010-07-08 Sol-Gel Technologies Ltd. Topical systems and kits

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
REDDY, V. R., SYNLETT, vol. 11, 2006, pages 1791
SCHMIDT, CHEM. UNSERER ZEIT, vol. 35, no. 3, 2001, pages 176

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014162311A1 (en) * 2013-04-01 2014-10-09 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. Adjustable sol-gel-based capsules comprising fragrances and aromas, and uses thereof
US9953588B1 (en) * 2014-03-25 2018-04-24 E Ink Corporation Nano-particle based variable transmission devices

Also Published As

Publication number Publication date
US8815786B2 (en) 2014-08-26
DE102011006315A1 (de) 2012-10-04
EP2691504B1 (de) 2016-11-16
EP2691504A1 (de) 2014-02-05
US20140024570A1 (en) 2014-01-23
ES2609630T3 (es) 2017-04-21
DE102011006315A8 (de) 2012-12-20

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