EP3497195B1 - Laundry composition - Google Patents

Laundry composition Download PDF

Info

Publication number
EP3497195B1
EP3497195B1 EP17742707.7A EP17742707A EP3497195B1 EP 3497195 B1 EP3497195 B1 EP 3497195B1 EP 17742707 A EP17742707 A EP 17742707A EP 3497195 B1 EP3497195 B1 EP 3497195B1
Authority
EP
European Patent Office
Prior art keywords
powder
silicone
powder composition
cationic polymer
cationic
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.)
Active
Application number
EP17742707.7A
Other languages
German (de)
French (fr)
Other versions
EP3497195A1 (en
Inventor
Amanda Jane Adams
Martin Charles Crossman
Philip Ronald Moore
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.)
Unilever Global IP Ltd
Unilever IP Holdings BV
Original Assignee
Unilever Global IP Ltd
Unilever IP Holdings BV
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=56618070&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP3497195(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever Global IP Ltd, Unilever IP Holdings BV filed Critical Unilever Global IP Ltd
Publication of EP3497195A1 publication Critical patent/EP3497195A1/en
Application granted granted Critical
Publication of EP3497195B1 publication Critical patent/EP3497195B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • C11D17/0034Fixed on a solid conventional detergent ingredient
    • 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
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents ; Methods for using cleaning compositions
    • C11D11/0082Special methods for preparing compositions containing mixtures of detergents ; Methods for using cleaning compositions one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
    • 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
    • C11D17/042Water soluble or water disintegrable containers or substrates containing cleaning compositions or additives for cleaning compositions
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/128Aluminium silicates, e.g. zeolites
    • 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
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • C11D3/227Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin with nitrogen-containing groups
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines

Definitions

  • the present invention concerns a powder composition for use in laundry.
  • the powder may be used to provide softening benefits.
  • Silicones are known in the art to provide softening benefits for example WO 2006/005068 (The Procter & Gamble Company ) discloses liquid laundry detergent compositions containing functionalised silicone materials as fabric care agents. WO 2015/078692 discloses that fabric softening silicones have been used to provide softness to fabrics from a laundry detergent composition.
  • EP 1561803 discloses a need to improve the fabric-softening performance of a laundry detergent composition without unduly negatively affecting its fabric-cleaning performance.
  • an auxiliary composition for use in the laundering or treatment of fabrics, comprising a co-particulate admix, the co-particulate ad-mix comprising: i) clay; and ii) a hydrophobic component that is a silicone; and iii) a cationic polymeric fabric-softening boosting component that is a cationic guar gum; ...
  • co-particulate admix is obtained by a process comprising the steps of contracting the hydrophobic component with the clay and the charged polymeric fabric-softening boosting component to form a mixture, and then agglomerating the mixture in a high shear mixer and/or a low shear mixer to form a co-particulate admix.
  • Further powder laundry compositions are disclosed in WO 2007/028773 , WO 2012/075611 and EP 1561806 .
  • zeolite provides improved carrying capacity for a softening silicone and cationic polymers mix.
  • a powder composition for laundry comprising:
  • the present invention relates to a powder composition.
  • the powder composition may be used in a powder form or formed into a whole or part of a tablet or solid structure.
  • the powder composition may be utilised as a laundry product on its own to provide softening benefits for example as an ancillary product.
  • the powder composition may be integrated into another laundry product to provide an additional softening benefit e.g. added to a powdered laundry detergent, added to a unit dose capsule or incorporated into a tablet.
  • the powder forms part of a unit dose capsule or tablet, preferably the powder is contained in a unit does capsule. More preferably the powder is contained in a unit dose capsule which further comprises a detergent composition. Preferably the detergent composition is in a separate compartment to the powder.
  • the silicones suitable for the present invention are fabric softening silicones.
  • Non-limiting examples of such silicones include: non-functionalised silicones such as polydimethylsiloxane (PDMS) or alkyl (or alkoxy) functional silicones, and functionalised silicones or copolymers with one or more different types of functional groups such as amino, phenyl, polyether, acrylate, siliconhydride, carboxy acid, quarternized nitrogen etc.
  • the molecular weight of the softening silicone is less than 150 000 g/mol, more preferably the molecular weight is less than 125 000 g/mol, most preferably the molecular weight is less than 105 00 g/mol.
  • the molecular weight can be from 500 to 150 000 g/mol, more preferably the molecular weight 500 to 125 000 g/mol, most preferably the molecular weight is 500 to 105 00 g/mol.
  • the viscosity of the silicone is preferably 500 to 11 000 cP as measured at 25°C using a TA Instruments Discovery HR-2 rheometer. Viscosity is determined at a range of shear rates between 0.1s-1 and 10s-1 and the largest value taken as the viscosity.
  • Preferred silicones are selected from polydialkylsiloxanes, anionic silicones and mixtures thereof.
  • the silicones are selected from polydialkylsiloxanes, amino functionalised silicones, carboxyl functionalised silicone and mixtures thereof.
  • Commercially available examples are Wacker SLM 441075, SFD209 (Ex Dow Corning) or X-22-3014E (ShinEtsu) DOW CORNING ® 2-8566 AMINO FLUID and DOW CORNING ® 200 FLUID. Mixtures of silicones may be used.
  • the silicone may be in the form of an emulsion or a fluid. It is preferably a silicone fluid.
  • the cationic polymer may also be referred to as a deposition polymer, this aids the delivery of the silicone composition to the textile surface.
  • the cationic polymer may be naturally derived or synthetic.
  • suitable cationic polymers include: cationic guars, acrylate polymers, cationic starches, cationic amino resins, cationic urea resins, and cationic polysaccharides; preferably cationic celluloses.
  • the cationic polymer is selected from; cationic guars, cationic cellulose, and cationic acrylate polymers.
  • Cationic hydroxyethyl cellulose is a particularly preferred cationic cellulose.
  • a particularly preferred class of cationic polymer is cationic celloluse ethers.
  • ethers are commercially available under the tradename Ucare LR-400 ([2-hydroxy- 3 (trimethylammonio) propyl ] -w-hydroxypoly (oxy-1, 2- ethanediyl) chloride) or the Jaguar polymers such as Guar hydroxypropyl trimonium chloride, Jaguar C13 ex Rhodia.
  • the molecular weight of the cationic polymer is preferably greater than 50 000 g/mol, more preferably greater than 100 000 g/mol.
  • the molecular weight is preferably less than 5 000 000 g/mol.
  • the carrier material for the silicone composition and cationic polymer is a zeolite.
  • Zeolites are microporous crystalline aluminosilicate minerals.
  • the zeolite is preferably of type A, P or X, or mixtures thereof.
  • a more preferred type of zeolite is type MAP - maximum aluminium zeolite P (zeolite MAP) as described and claimed in EP 384 070A (Unilever ).
  • MAP is defined as an alkali metal aluminosilicate of zeolite P type having a silicon to aluminium ratio not exceeding 1.33, preferably within the range of from 0.90 to 1.33, more preferably within the range of from 0.90 to 1.20.
  • zeolite MAP having a silicon to aluminium ratio not exceeding 1.07, more preferably 1.00.
  • Commercially available zeolites include zeolite 4A, A28 and A24 available under the Doucil ® trademark from PQ Corporation.
  • a particularly preferred zeolite for the present invention is Doucil A24 ex. PQ Corporation.
  • the particle pour size of the zeolite is 0.05 to 1um, more preferably 0.1 to 0.5um.
  • ingredients may be loaded onto the carrier material in addition to the silicone and cationic polymer. These may, for example be other laundry ingredients, benefit agents or materials providing an enhanced consumer experience.
  • Some particularly preferred optional ingredients include:
  • Free oil perfumes and fragrances may be added to the powder composition. These may be to scent the powder, to provide scent in the washing process or to provide scent to the textiles after the wash.
  • the powders of the present invention may comprise one or more perfumes if desired.
  • the perfume is preferably present in an amount from 0.01 to 10 % by weight, more preferably from 0.05 to 5 % by weight, even more preferably from 0.1 to 4.0 %, most preferably from 0.15 to 4.0 % by weight, based on the total weight of the composition.
  • Useful components of the perfume include materials of both natural and synthetic origin. They include single compounds and mixtures. Specific examples of such components may be found in the current literature, e.g., in Fenaroli's Handbook of Flavor Ingredients, 1975, CRC Press ; Synthetic Food Adjuncts, 1947 by M. B. Jacobs, edited by Van Nostr and; or Perfume and Flavor Chemicals by S. Arctander 1969, Montclair, N.J. (USA ). These substances are well known to the person skilled in the art of perfuming, flavouring, and/or aromatizing consumer products.
  • Particularly preferred perfume ingredients are blooming perfume ingredients and substantive perfume ingredients. Blooming perfume ingredients are defined by a boiling point less than 250°C and a LogP ogreater than 2.5. Substantive perfume ingredients are defined by a boiling point greater than 250°C and a LogP greater than 2.5. Preferably a perfume composition will comprise a mixture of blooming and substantive perfume ingredients. The perfume composition may comprise other perfume ingredients.
  • perfume components it is commonplace for a plurality of perfume components to be present in a formulation.
  • compositions for use in the present invention it is envisaged that there will be three or more, preferably four or more, more preferably five or more, most preferably six or more different perfume components.
  • An upper limit of 300 perfume ingredients may be applied.
  • Colour may optionally be provided to the powder by the addition of one or more colorants.
  • the colorant comprises one or more dyes and/or pigments.
  • the pigment/dye may be any colour. These may be substantive or non-substantive dyes/pigments. A preferred level is one where the colour is discernible to the consumer and aesthetically pleasing.
  • the powder may be a plurality of colours.
  • the powder of the present invention may further comprise microcapsules encapsulating a benefit agent.
  • Suitable encapsulating material may comprise, but are not limited to; aminoplasts, proteins, polyurethanes, polyacrylates, polymethacrylates, polysaccharides, polyamides, polyolefins, gums, silicones, lipids, modified cellulose, polyphosphate, polystyrene, polyesters or combinations thereof.
  • Preferred benefit agents include perfumes, lubricants and any other oily materials. Particularly preferred benefit agents include, but are not limited to, the following:
  • perfume components include both odiferous materials and pro-fragrance materials.
  • perfume ingredients particularly preferred perfume ingredients are blooming perfume ingredients and substantive perfume ingredients. Blooming perfume ingredients are defined by a boiling point less than 250°C and a LogP ogreater than 2.5. Substantive perfume ingredients are defined by a boiling point greater than 250°C and a LogP greater than 2.5.
  • a perfume composition will comprise a mixture of blooming and substantive perfume ingredients. The perfume composition may comprise other perfume ingredients.
  • perfume components it is commonplace for a plurality of perfume components to be present in a formulation.
  • compositions for use in the present invention it is envisaged that there will be three or more, preferably four or more, more preferably five or more, most preferably six or more different perfume components.
  • An upper limit of 300 perfume ingredients may be applied.
  • the powder composition of the present invention comprises 60 to 85 w.t. % zeolite, more preferably 65 to 85 w.t. %, most preferably 65 to 80 w.t. %.
  • the powder composition of the present invention comprises 15 to 35 w.t. %, most preferably 20 to 35 w.t. % a combined weight of silicone and cationic polymer.
  • the ratio of silicone to cationic polymer is between 5:4 and 10:1, preferably between 5:4 and 8:1, more preferably between 5:4 and 6:1 and most preferably between 5:3 and 5:1.
  • the final laundry product comprising the powder of the present invention comprises 10 to 30 w.t. % silicone, more preferably, 15 to 25 w.t. % silicone.
  • the silicone, cationic polymer and carrier comprise at least 90 w.t. % of the powder composition. More preferably the silicone, cationic polymer and carrier comprise at least 95 w.t. % of the powder composition.
  • the powder of the present invention may in one embodiment be prepared by the following method:
  • the other laundry product my for example be a powder laundry detergent, a laundry tablet, or a laundry unit dose capsule.
  • the powder is used for softening benefits in other words as a softening booster for textiles.
  • the powder may be incorporated into another laundry product or may be for use as a separate, stand-alone product which can be added during the wash process for a softening boost.
  • the carrier material was added in to a Cutter C6 (ex. Sirman) mixer which was fitted with dough mix blades, and the mixer turned on.
  • the carboxysilicone 1 and cationically modified polymer 2 where mixed separately and slowly dripped into the mixer while the mixer was running. Mixing was continued for a short period to ensure thorough mixing.
  • the resulting powder was assessed visually. Dry powders which can flow more easily demonstrate higher loading capacity of the silicone, polymer mix. Damp and sticky powders demonstrate a lower loading capacity for the silicone, polymer mix.
  • the powder was loaded into a cylinder and the surface levelled.
  • a 10 kg consolidation weight was placed slowly on top of the powder and allowed to remain in position for 2 minutes. The weight was then removed and the cylinder removed carefully from the powder to leave a free-standing briquette of powder.
  • zeolite For the zeolite: If the briquette remained standing, a 200g weight was placed on the top of the briquette. If after 10 seconds the briquette was still standing, a 100g weight was added. 100g weights continued to be added until the briquette collapsed.
  • the cohesiveness of a powder is classified by the weight (w.t.) as follows:
  • the visual assessment of the zeolite carrier compared to the bentonite clay demonstrates that the zeolite can carry more silicone and cationic polymer mix than the bentonite, while maintaining the properties of a flowing powder. Flowing powders are necessary for the processing and use of laundry products.
  • the UTC results demonstrate that the zeolite carrier has a moderate flow / has improved flow compared to the bentonite clay which was cohesive and required significantly more weight to make the briquette collapse. If the carrier is a poor carrier and does not hold all of the silicone and cationic polymer mix, the powder sticks together and can support weights. However if the silicone and cationic polymer mix is carried well, the carrier is a free flowing powder which falls apart when weights are place on top.

Description

    Technical Field
  • The present invention concerns a powder composition for use in laundry. The powder may be used to provide softening benefits.
  • Background to the Invention
  • Textile fabrics, including clothes, have traditionally been cleaned with laundry detergents. After cleaning, fabrics can often feel harsh. To prevent this, especially harshness experienced after multiple wash cycles, technologies have been developed to increase the softness of fabrics, including rinse-added conditioner compositions and softening systems added to the detergent composition.
  • Silicones are known in the art to provide softening benefits for example WO 2006/005068 (The Procter & Gamble Company ) discloses liquid laundry detergent compositions containing functionalised silicone materials as fabric care agents. WO 2015/078692 discloses that fabric softening silicones have been used to provide softness to fabrics from a laundry detergent composition.
  • EP 1561803 (The Procter & Gamble Company ) discloses a need to improve the fabric-softening performance of a laundry detergent composition without unduly negatively affecting its fabric-cleaning performance. There is disclosed an auxiliary composition, for use in the laundering or treatment of fabrics, comprising a co-particulate admix, the co-particulate ad-mix comprising: i) clay; and ii) a hydrophobic component that is a silicone; and iii) a cationic polymeric fabric-softening boosting component that is a cationic guar gum; ... wherein the co-particulate admix is obtained by a process comprising the steps of contracting the hydrophobic component with the clay and the charged polymeric fabric-softening boosting component to form a mixture, and then agglomerating the mixture in a high shear mixer and/or a low shear mixer to form a co-particulate admix. Further powder laundry compositions are disclosed in WO 2007/028773 , WO 2012/075611 and EP 1561806 .
  • Statement of the Invention
  • It has been found that zeolite provides improved carrying capacity for a softening silicone and cationic polymers mix.
  • A powder composition for laundry, comprising:
    1. a. Fabric softening silicone;
    2. b. cationic polymer; and
    3. c. 60 to 85 wt. % zeolite;
    wherein the silicone composition and cationic polymer are loaded onto the carrier, wherein the carrier is the zeolite and the combined weight of silicone and cationic polymer is 15 to 35 wt. % of the powder composition; wherein the molecular weight of the softening silicone is less than 150 000g/mol.
  • In a second aspect of the present invention is provided a method of producing the powder composition as disclosed herein comprising the steps of:
    • Preparing a premix of silicone and cationic polymer
    • Adding the premix to the zeolite
    • Mixing
    • Optionally adding the powder to a separate laundry product
  • In a third aspect of the present invention is provided a use of the powder composition as disclosed herein for softening textiles.
  • Detailed Description of the Invention Form of the Invention
  • The present invention relates to a powder composition. The powder composition may be used in a powder form or formed into a whole or part of a tablet or solid structure. The powder composition may be utilised as a laundry product on its own to provide softening benefits for example as an ancillary product. Alternatively the powder composition may be integrated into another laundry product to provide an additional softening benefit e.g. added to a powdered laundry detergent, added to a unit dose capsule or incorporated into a tablet.
  • In one embodiment the powder forms part of a unit dose capsule or tablet, preferably the powder is contained in a unit does capsule. More preferably the powder is contained in a unit dose capsule which further comprises a detergent composition. Preferably the detergent composition is in a separate compartment to the powder.
  • It is important that the powder is not sticky, this would cause problems with processing and the ability to mix the powder into other products.
  • Silicone Composition
  • The silicones suitable for the present invention are fabric softening silicones. Non-limiting examples of such silicones include: non-functionalised silicones such as polydimethylsiloxane (PDMS) or alkyl (or alkoxy) functional silicones, and functionalised silicones or copolymers with one or more different types of functional groups such as amino, phenyl, polyether, acrylate, siliconhydride, carboxy acid, quarternized nitrogen etc.
  • The molecular weight of the softening silicone is less than 150 000 g/mol, more preferably the molecular weight is less than 125 000 g/mol, most preferably the molecular weight is less than 105 00 g/mol.
  • In one embodiment the molecular weight can be from 500 to 150 000 g/mol, more preferably the molecular weight 500 to 125 000 g/mol, most preferably the molecular weight is 500 to 105 00 g/mol.
  • The viscosity of the silicone is preferably 500 to 11 000 cP as measured at 25°C using a TA Instruments Discovery HR-2 rheometer. Viscosity is determined at a range of shear rates between 0.1s-1 and 10s-1 and the largest value taken as the viscosity.
  • Preferred silicones are selected from polydialkylsiloxanes, anionic silicones and mixtures thereof.
  • Most preferably the silicones are selected from polydialkylsiloxanes, amino functionalised silicones, carboxyl functionalised silicone and mixtures thereof. Commercially available examples are Wacker SLM 441075, SFD209 (Ex Dow Corning) or X-22-3014E (ShinEtsu) DOW CORNING® 2-8566 AMINO FLUID and DOW CORNING® 200 FLUID. Mixtures of silicones may be used.
  • The silicone may be in the form of an emulsion or a fluid. It is preferably a silicone fluid.
  • Cationic Polymer
  • The cationic polymer may also be referred to as a deposition polymer, this aids the delivery of the silicone composition to the textile surface.
  • The cationic polymer may be naturally derived or synthetic. Examples of suitable cationic polymers include: cationic guars, acrylate polymers, cationic starches, cationic amino resins, cationic urea resins, and cationic polysaccharides; preferably cationic celluloses.
  • Preferably the cationic polymer is selected from; cationic guars, cationic cellulose, and cationic acrylate polymers. Cationic hydroxyethyl cellulose is a particularly preferred cationic cellulose.
  • A particularly preferred class of cationic polymer is cationic celloluse ethers. Such ethers are commercially available under the tradename Ucare LR-400 ([2-hydroxy- 3 (trimethylammonio) propyl ] -w-hydroxypoly (oxy-1, 2- ethanediyl) chloride) or the Jaguar polymers such as Guar hydroxypropyl trimonium chloride, Jaguar C13 ex Rhodia.
  • The molecular weight of the cationic polymer is preferably greater than 50 000 g/mol, more preferably greater than 100 000 g/mol. The molecular weight is preferably less than 5 000 000 g/mol.
  • Carrier Material
  • The carrier material for the silicone composition and cationic polymer is a zeolite. Zeolites are microporous crystalline aluminosilicate minerals.
  • The zeolite is preferably of type A, P or X, or mixtures thereof. A more preferred type of zeolite is type MAP - maximum aluminium zeolite P (zeolite MAP) as described and claimed in EP 384 070A (Unilever ). MAP is defined as an alkali metal aluminosilicate of zeolite P type having a silicon to aluminium ratio not exceeding 1.33, preferably within the range of from 0.90 to 1.33, more preferably within the range of from 0.90 to 1.20. Especially preferred is zeolite MAP having a silicon to aluminium ratio not exceeding 1.07, more preferably 1.00. Commercially available zeolites include zeolite 4A, A28 and A24 available under the Doucil ® trademark from PQ Corporation. A particularly preferred zeolite for the present invention is Doucil A24 ex. PQ Corporation.
  • Preferably the particle pour size of the zeolite is 0.05 to 1um, more preferably 0.1 to 0.5um.
  • Other Components
  • Other ingredients may be loaded onto the carrier material in addition to the silicone and cationic polymer. These may, for example be other laundry ingredients, benefit agents or materials providing an enhanced consumer experience.
  • Some particularly preferred optional ingredients include:
  • Free oil perfumes
  • Free oil perfumes and fragrances may be added to the powder composition. These may be to scent the powder, to provide scent in the washing process or to provide scent to the textiles after the wash.
  • The powders of the present invention may comprise one or more perfumes if desired. The perfume is preferably present in an amount from 0.01 to 10 % by weight, more preferably from 0.05 to 5 % by weight, even more preferably from 0.1 to 4.0 %, most preferably from 0.15 to 4.0 % by weight, based on the total weight of the composition.
  • Useful components of the perfume include materials of both natural and synthetic origin. They include single compounds and mixtures. Specific examples of such components may be found in the current literature, e.g., in Fenaroli's Handbook of Flavor Ingredients, 1975, CRC Press; Synthetic Food Adjuncts, 1947 by M. B. Jacobs, edited by Van Nostrand; or Perfume and Flavor Chemicals by S. Arctander 1969, Montclair, N.J. (USA). These substances are well known to the person skilled in the art of perfuming, flavouring, and/or aromatizing consumer products.
  • Particularly preferred perfume ingredients are blooming perfume ingredients and substantive perfume ingredients. Blooming perfume ingredients are defined by a boiling point less than 250°C and a LogP ogreater than 2.5. Substantive perfume ingredients are defined by a boiling point greater than 250°C and a LogP greater than 2.5. Preferably a perfume composition will comprise a mixture of blooming and substantive perfume ingredients. The perfume composition may comprise other perfume ingredients.
  • It is commonplace for a plurality of perfume components to be present in a formulation. In the compositions for use in the present invention it is envisaged that there will be three or more, preferably four or more, more preferably five or more, most preferably six or more different perfume components. An upper limit of 300 perfume ingredients may be applied.
  • Colourants
  • Colour may optionally be provided to the powder by the addition of one or more colorants. The colorant comprises one or more dyes and/or pigments. The pigment/dye may be any colour. These may be substantive or non-substantive dyes/pigments. A preferred level is one where the colour is discernible to the consumer and aesthetically pleasing. The powder may be a plurality of colours.
  • Microcapsules
  • The powder of the present invention may further comprise microcapsules encapsulating a benefit agent. Suitable encapsulating material, may comprise, but are not limited to; aminoplasts, proteins, polyurethanes, polyacrylates, polymethacrylates, polysaccharides, polyamides, polyolefins, gums, silicones, lipids, modified cellulose, polyphosphate, polystyrene, polyesters or combinations thereof.
  • Preferred benefit agents include perfumes, lubricants and any other oily materials. Particularly preferred benefit agents include, but are not limited to, the following:
    1. a) silicone oils, resins, and modifications thereof such as linear and cyclic polydimethylsiloxanes, amino-modified, allcyl, aryl, and alkylaryl silicone oils, which preferably have a viscosity of greater than 50,000 cst;
    2. b) perfume components including fragrance, perfumery, and essential oils and resins, aromatherapy actives and pro-fragrance materials;
    3. c) insect repellants
    4. d) organic sunscreen actives, for example, octylmethoxy cinnamate;
    5. e) antimicrobial agents, for example, 2-hydroxy-4, 2,4- trichlorodiphenylether;
    6. f) ester solvents; for example, isopropyl myristate;
    7. g) lipids and lipid like substance, for example, cholesterol;
    8. h) hydrocarbons such as paraffins, petrolatum, and mineral oil
    9. i) fish and vegetable oils;
    10. j) hydrophobic plant extracts;
    11. k) waxes;
    12. l) pigments including inorganic compounds with hydrophobically- modified surface and/ or dispersed in an oil or a hydrophobic liquid, and;
    13. m) sugar-esters, such as sucrose polyester (SPE).
  • The most preferred benefit agents are perfume components. Perfume components include both odiferous materials and pro-fragrance materials.
  • When the microcapsule comprises perfume ingredients, particularly preferred perfume ingredients are blooming perfume ingredients and substantive perfume ingredients. Blooming perfume ingredients are defined by a boiling point less than 250°C and a LogP ogreater than 2.5. Substantive perfume ingredients are defined by a boiling point greater than 250°C and a LogP greater than 2.5. Preferably a perfume composition will comprise a mixture of blooming and substantive perfume ingredients. The perfume composition may comprise other perfume ingredients.
  • It is commonplace for a plurality of perfume components to be present in a formulation. In the compositions for use in the present invention it is envisaged that there will be three or more, preferably four or more, more preferably five or more, most preferably six or more different perfume components. An upper limit of 300 perfume ingredients may be applied.
  • Loading and carrying capacity
  • The powder composition of the present invention comprises 60 to 85 w.t. % zeolite, more preferably 65 to 85 w.t. %, most preferably 65 to 80 w.t. %.
  • The powder composition of the present invention comprises 15 to 35 w.t. %, most preferably 20 to 35 w.t. % a combined weight of silicone and cationic polymer.
  • The ratio of silicone to cationic polymer is between 5:4 and 10:1, preferably between 5:4 and 8:1, more preferably between 5:4 and 6:1 and most preferably between 5:3 and 5:1.
  • It is preferred that the final laundry product comprising the powder of the present invention comprises 10 to 30 w.t. % silicone, more preferably, 15 to 25 w.t. % silicone.
  • Preferably the silicone, cationic polymer and carrier comprise at least 90 w.t. % of the powder composition. More preferably the silicone, cationic polymer and carrier comprise at least 95 w.t. % of the powder composition.
  • Method of production
  • The powder of the present invention, may in one embodiment be prepared by the following method:
    • Preparing a premix of silicone and cationic polymer
    • Adding the premix to the zeolite
    • Mixing
    • Optionally adding the powder to another laundry product
  • The other laundry product my for example be a powder laundry detergent, a laundry tablet, or a laundry unit dose capsule.
  • Use of the powder
  • In one embodiment of the current invention, the powder is used for softening benefits in other words as a softening booster for textiles. The powder may be incorporated into another laundry product or may be for use as a separate, stand-alone product which can be added during the wash process for a softening boost.
  • Examples Preparation of the powder
  • The carrier material was added in to a Cutter C6 (ex. Sirman) mixer which was fitted with dough mix blades, and the mixer turned on. The carboxysilicone1 and cationically modified polymer2 where mixed separately and slowly dripped into the mixer while the mixer was running. Mixing was continued for a short period to ensure thorough mixing.
  • Visual assessment of the powder
  • The resulting powder was assessed visually. Dry powders which can flow more easily demonstrate higher loading capacity of the silicone, polymer mix. Damp and sticky powders demonstrate a lower loading capacity for the silicone, polymer mix.
  • Unconfined compression test
  • In this test, the freshly produced powders were compressed into a compact briquette and the force required to break the briquette was measured.
  • The powder was loaded into a cylinder and the surface levelled. A 10 kg consolidation weight was placed slowly on top of the powder and allowed to remain in position for 2 minutes. The weight was then removed and the cylinder removed carefully from the powder to leave a free-standing briquette of powder.
  • For the clay: If the briquette remained standing, a 200g weight was placed on the top of the briquette. If after 10 seconds the briquette was still standing, a 250g weight was placed on top of the briquette. If after 10 seconds the briquette was still standing, a 100g weight was added. 100g weights continued to be added until the briquette collapsed.
  • For the zeolite: If the briquette remained standing, a 200g weight was placed on the top of the briquette. If after 10 seconds the briquette was still standing, a 100g weight was added. 100g weights continued to be added until the briquette collapsed.
  • The total weight (w.t.) needed to effect collapse is noted.
  • The cohesiveness of a powder is classified by the weight (w.t.) as follows:
    • < 1.0 kg Good flowing
    • 1.0 kg < w.t. < 2.0 kg Moderate flowing.
    • 2.0 kg < w.t. < 5.0 kg Cohesive.
    Table 1
    Carrier type Carrier Cationic polymer2 Carboxysilicone1 Visual Assessment UCT (w.t.) Flow assessment based on UTC result
    (g) w.t.% (g) w.t.% (g) w.t.%
    Bentonite clay3 584 73.06 61.5 7.69 153.8 19.24 Sticky damp powder 3450g Cohesive
    Zeolite4 584 73.14 61.5 7.70 153 19.16 Free flowing powder 1200g Moderate flowing
    1 -
    Carboxy functionalised silicone SLM 441075 ex. Waker, having a visocisty of 2 000 Pascal seconds as measured as above and a molecular weight of less than 50 000 g/mol
    2 -
    UCARE™ Ploymer LR400 ex. Dow
    3 -
    Bentonite ex. Sigma-Aldrich
    4 -
    Doucil A24 Zeolite ex. PQ Corporation
  • The visual assessment of the zeolite carrier compared to the bentonite clay demonstrates that the zeolite can carry more silicone and cationic polymer mix than the bentonite, while maintaining the properties of a flowing powder. Flowing powders are necessary for the processing and use of laundry products.
  • The UTC results also demonstrate that the zeolite carrier has a moderate flow / has improved flow compared to the bentonite clay which was cohesive and required significantly more weight to make the briquette collapse. If the carrier is a poor carrier and does not hold all of the silicone and cationic polymer mix, the powder sticks together and can support weights. However if the silicone and cationic polymer mix is carried well, the carrier is a free flowing powder which falls apart when weights are place on top.

Claims (12)

  1. A powder composition for laundry, comprising:
    a. Fabric softening silicone;
    b. cationic polymer; and
    c. 60 to 85 wt. % zeolite;
    wherein the silicone composition and cationic polymer are loaded onto the carrier, wherein the carrier is the zeolite and the combined weight of silicone and cationic polymer is 15 to 35 wt. % of the powder composition;
    wherein the molecular weight of the softening silicone is less than 150 000g/mol.
  2. A powder according to claim 1, wherein the silicone, cationic polymer and carrier comprise at least 90 wt. % of the powder composition.
  3. A powder composition according to claim 1 wherein the silicone is selected from polydialkylsiloxanes, anionic silicones and mixtures thereof.
  4. A powder composition according to any preceding claim, wherein a final laundry product comprising the powder of the present invention comprises 10 to 30 wt. % silicone.
  5. A powder composition according to any preceding claim wherein the carrier is a type A, P or X zeolite, or mixtures thereof.
  6. A powder composition according to any preceding claim wherein the cationic polymer is selected from: cationic guars, cationic cellulose and cationic acrylate polymers.
  7. A powder composition according to any preceding claim, wherein the ratio of silicone to cationic polymer is between 5:4 and 10:1.
  8. A unit dose capsule containing the powder composition according to any preceding claim.
  9. A unit dose capsule according to claim 8, further containing a detergent composition.
  10. A unit dose capsule according to claim 9, wherein the detergent composition is in a separate compartment of a unit dose to the powder.
  11. A method of producing the powder composition according to claims 1 to 7 comprising the steps of:
    - Preparing a premix of silicone and cationic polymer
    - Adding the premix to the zeolite
    - Mixing
    - Optionally adding the powder to another laundry product
  12. Use of the powder composition according to claims 1 to 7 for softening textiles.
EP17742707.7A 2016-08-10 2017-07-13 Laundry composition Active EP3497195B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP16183548 2016-08-10
PCT/EP2017/067793 WO2018028928A1 (en) 2016-08-10 2017-07-13 Laundry composition

Publications (2)

Publication Number Publication Date
EP3497195A1 EP3497195A1 (en) 2019-06-19
EP3497195B1 true EP3497195B1 (en) 2022-09-07

Family

ID=56618070

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17742707.7A Active EP3497195B1 (en) 2016-08-10 2017-07-13 Laundry composition

Country Status (5)

Country Link
EP (1) EP3497195B1 (en)
CN (1) CN109563444A (en)
AR (1) AR109309A1 (en)
WO (1) WO2018028928A1 (en)
ZA (1) ZA201900668B (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003057815A1 (en) 2002-01-07 2003-07-17 Ciba Specialty Chemicals Holding Inc. Particulate composition comprising dye fixatives
WO2007028773A1 (en) 2005-09-06 2007-03-15 Dow Corning Corporation Delivery system for releasing silicone ingredients
WO2008128826A1 (en) 2007-04-23 2008-10-30 Henkel Ag & Co. Kgaa Particles containing photocatalytic material
US20140352076A1 (en) 2013-05-31 2014-12-04 Haiyan Song Laundry detergents

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2001927C (en) 1988-11-03 1999-12-21 Graham Thomas Brown Aluminosilicates and detergent compositions
ATE454439T1 (en) * 2004-02-03 2010-01-15 Procter & Gamble LAUNDRY CLEANING OR TREATMENT COMPOSITION AND A PROCESS FOR PRODUCING THE COMPOSITION
EP1561803B1 (en) * 2004-02-03 2008-04-23 The Procter & Gamble Company A composition for use in the laundering or treatment of fabrics
US20060003913A1 (en) 2004-06-30 2006-01-05 The Procter & Gamble Company Perfumed liquid laundry detergent compositions with functionalized silicone fabric care agents
GB0818025D0 (en) * 2008-10-02 2008-11-05 Dow Corning Granular composition
WO2012075611A1 (en) * 2010-12-10 2012-06-14 The Procter & Gamble Company Laundry detergents
EP3074495B1 (en) 2013-11-27 2017-07-05 Unilever Plc. Laundry compositions

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003057815A1 (en) 2002-01-07 2003-07-17 Ciba Specialty Chemicals Holding Inc. Particulate composition comprising dye fixatives
WO2007028773A1 (en) 2005-09-06 2007-03-15 Dow Corning Corporation Delivery system for releasing silicone ingredients
WO2008128826A1 (en) 2007-04-23 2008-10-30 Henkel Ag & Co. Kgaa Particles containing photocatalytic material
US20140352076A1 (en) 2013-05-31 2014-12-04 Haiyan Song Laundry detergents

Also Published As

Publication number Publication date
WO2018028928A1 (en) 2018-02-15
AR109309A1 (en) 2018-11-21
BR112019002478A2 (en) 2019-05-14
EP3497195A1 (en) 2019-06-19
ZA201900668B (en) 2021-06-30
CN109563444A (en) 2019-04-02

Similar Documents

Publication Publication Date Title
JP7038718B2 (en) Density-balanced, influential fragrance microcapsules
JP6214553B2 (en) Method for producing polyurea microcapsules
JP7416620B2 (en) Method for manufacturing microcapsules
KR102645458B1 (en) microcapsule
CN102858944B (en) Delivery of particles
CN103622842B (en) Delivery of particles
JP5670751B2 (en) Deposition of lipophilic active materials in compositions containing surfactants
US20130295149A1 (en) Polyurea microcapsules
BR112016001974B1 (en) PROCESS FOR THE PREPARATION OF A PARTICLE, PARTICLE OBTAINED FROM THE PROCESS, NET COMPOSITION, COMPOSITION FOR DOMESTIC CARE OR PERSONAL CARE AND METHOD OF TREATING A SUBSTRATE
CN106604715B (en) Use of benefit delivery particles for off-flavour benefits
MX2007001843A (en) Stabilized liquid rinse-off compositions comprising fragranced aminoplast capsules.
CN102892492A (en) Delivery particle
WO2010048154A2 (en) Structured composition comprising an encapsulated active
CN101389225A (en) Process for the preparation of powders from slurries of fragranced aminoplast capsules
BR112015008135B1 (en) particle, liquid composition and substrate treatment method
WO2015158635A1 (en) Capsules with a high active ingredient content
JP2021087956A (en) Method for preparation of microcapsules free from melamine-formaldehyde
WO2020233887A1 (en) Core-shell encapsulated composition comprising a benefit agent
BR112015010475B1 (en) particle, liquid composition and composition of home care or personal care
EP3497196B1 (en) Laundry composition
EP3497195B1 (en) Laundry composition
WO2018019908A1 (en) Process for the preparation of microcapsules
BR112019002478B1 (en) LAUNDRY POWDER COMPOSITION, METHOD OF PRODUCTION OF THE LAUNDRY POWDER COMPOSITION AND USE OF THE LAUNDRY POWDER COMPOSITION
BR112019002470B1 (en) POWDER COMPOSITION FOR LAUNDRY COMPOSITION, POWDER COMPOSITION PRODUCTION METHOD AND POWDER COMPOSITION USE
WO2023057238A1 (en) Fragrance encapsulated in microcapsules containing a shell obtained from polyisocyanate, alkyl silicate and polyethyleneimine

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20190115

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20200331

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UNILEVER GLOBAL IP LIMITED

Owner name: UNILEVER IP HOLDINGS B.V.

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20220125

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UNILEVER GLOBAL IP LIMITED

Owner name: UNILEVER IP HOLDINGS B.V.

GRAJ Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted

Free format text: ORIGINAL CODE: EPIDOSDIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTC Intention to grant announced (deleted)
INTG Intention to grant announced

Effective date: 20220412

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1517057

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220915

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602017061511

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20221207

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1517057

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20221208

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20230109

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20230107

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602017061511

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230428

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

26 Opposition filed

Opponent name: HENKEL AG & CO. KGAA

Effective date: 20230602

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20230721

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230719

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220907

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230713

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20230713