EP3516033B1 - Procédé de production en continu de corps fusibles contenant du parfum - Google Patents

Procédé de production en continu de corps fusibles contenant du parfum Download PDF

Info

Publication number
EP3516033B1
EP3516033B1 EP17771764.2A EP17771764A EP3516033B1 EP 3516033 B1 EP3516033 B1 EP 3516033B1 EP 17771764 A EP17771764 A EP 17771764A EP 3516033 B1 EP3516033 B1 EP 3516033B1
Authority
EP
European Patent Office
Prior art keywords
oil
melt
water
fragrance
polyquaternium
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
EP17771764.2A
Other languages
German (de)
English (en)
Other versions
EP3516033A1 (fr
Inventor
Thomas Holderbaum
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=61564513&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP3516033(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP3516033A1 publication Critical patent/EP3516033A1/fr
Application granted granted Critical
Publication of EP3516033B1 publication Critical patent/EP3516033B1/fr
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
    • 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
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents
    • C11D11/0082Special methods for preparing compositions containing mixtures of detergents 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
    • 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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3707Polyethers, e.g. polyalkyleneoxides
    • 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
    • C11D3/507Compounds releasing perfumes by thermal or chemical activation

Definitions

  • the present invention relates to a continuous process for the production of perfume-containing melting bodies comprising at least one water-soluble or water-dispersible carrier polymer with a melting point> 30 ° C. and at least one fragrance, comprising the process steps described here and the perfume-containing melting bodies produced in this way.
  • Fragrances in the form of fragrance particles are often either used as an integral part of a washing or cleaning agent, or are metered into the washing drum in a separate form directly at the start of a washing cycle. In this way, the consumer can control the scenting of the laundry to be washed by individual dosing.
  • Fragrance particles of this type are usually provided in the form of perfume-containing melting bodies in a batch process.
  • Such perfume-containing moldings produced from melts require that the perfume is exposed to higher temperatures during manufacture.
  • the finished product melt is then transferred into a shaped body by means of cooling. Any production disruptions mean that the melt has to stay at higher temperatures for a longer period of time. This can lead to the breakdown of thermolabile components, such as some perfume components.
  • the melting of the ingredients of the shaped body, including the perfume results in the latter being exposed to unnecessarily long, high temperatures, which can also be disadvantageous for the reasons mentioned above.
  • the object of the present invention was therefore to overcome the problems mentioned above in the production of perfume-containing melting bodies.
  • the object was achieved according to the invention by a continuous process in which one or more constituents of the shaped body, i.e. usually the at least one carrier polymer, the fragrances are metered in continuously.
  • a continuous process in which one or more constituents of the shaped body, i.e. Usually the at least one carrier polymer is melted and the fragrances are metered in continuously to the melt.
  • melt is meant a composition that can be pumped, pumped and flowed.
  • the melt comprising the at least one water-soluble or water-dispersible carrier polymer, which according to the present invention is continuously conveyed, can be produced spatially decoupled from the conveyance.
  • At least one refers to 1 or more, for example 1, 2, 3, 4, 5, 6, 7, 8, 9 or more. In particular, this information relates to the type of agent / compound and not the absolute number of molecules. "At least one fragrance” therefore means that at least one type of fragrance is detected, but 2 or more different types of fragrances can also be contained.
  • the melting bodies obtained are solid at room temperature and temperatures up to 30 ° C., preferably up to 40 ° C.
  • the at least one carrier polymer is distinguished by the fact that it has a melting point of from 48 ° C. to 120 ° C., preferably from 48 ° C. to 80 ° C.
  • Water soluble as used herein means a solubility in water at 20 ° C of at least 1 g / L, preferably at least 10 g / L, more preferably at least 50 g / L.
  • Water dispersible as used herein means that the carrier polymer can be dispersed in water at a temperature of 20 ° C using known methods.
  • the at least one carrier polymer is preferably selected from polyalkylene glycols.
  • Suitable polyalkylene glycols in the context of the present invention are those which have an average molecular weight of> 1000 g / mol, in particular> 1500 g / mol, preferably an average molecular weight between 3,000 and 15,000, more preferably an average molecular weight between 4,000 and 13,000 and particularly preferably have average molecular weight between 9,000 and 12,000.
  • those polyalkyl glycols are particularly suitable which have a melting point between 40 ° C. and 90 ° C., in particular in the range from 45 to 70 ° C.
  • Examples of polyalkylene glycols that are useful in the context of the present invention are polypropylene glycol and polyethylene glycol.
  • the at least one carrier polymer is preferably polyethylene glycol.
  • the at least one carrier polymer is a polyethylene glycol with an average molecular weight of> 1500 g / mol, preferably an average molecular weight between 3,000 and 15,000, more preferably with an average molecular weight between 4,000 and 13,000 and particularly preferably with an average Molecular weight between 6,000 and 8,000 or 9,000 to 12,000.
  • a polyethylene glycol is characterized by a melting point in the range from 45 to 70 ° C., preferably 50 to 65 ° C., more preferably 50 to 60 ° C.
  • the at least one carrier polymer is contained in the melting body in an amount of 30 to 95% by weight, preferably 35 to 85% by weight, for example 40 to 80 or 40 to 78% by weight, based on the Total weight of the melting body
  • Another component of the melting body is at least one fragrance.
  • a fragrance is a chemical substance that stimulates the sense of smell. In order to stimulate the sense of smell, the chemical substance should be at least partially dispersible in the air, ie the fragrance should be at least slightly volatile at 25 ° C. If the fragrance is very volatile, the intensity of the smell will quickly fade away. With a lower volatility, however, the smell impression is more sustainable, ie it does not disappear so quickly.
  • the fragrance therefore has a melting point which is in the range from -100 ° C. to 100 ° C., preferably from -80 ° C. to 80 ° C., more preferably from -20 ° C. to 50 ° C., in particular from 30 ° C to 20 ° C.
  • the fragrance has a boiling point which is in the range from 25 ° C. to 400 ° C., preferably from 50 ° C. to 380 ° C., more preferably from 75 ° C. to 350 ° C., in particular from 100 ° C. to 330 ° C.
  • the fragrance has a molecular weight of 40 to 700 g / mol, more preferably 60 to 400 g / mol.
  • fragrance The smell of a fragrance is perceived by most people as pleasant and often corresponds to the smell of, for example, flowers, fruits, spices, bark, resin, Leaves, grasses, mosses and roots. Fragrances can also be used to mask unpleasant smells or to provide a non-smelling substance with a desired smell.
  • Individual fragrance compounds for example synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type, can be used as fragrances.
  • Perfume compounds of the aldehyde type are, for example, adoxal (2,6,10-trimethyl-9-undecenal), anisaldehyde (4-methoxybenzaldehyde), cymal (3- (4-isopropylphenyl) -2-methylpropanal), ethylvanillin, florhydral ( 3- (3-isopropylphenyl) butanal), helional (3- (3,4-methylenedioxyphenyl) -2-methylpropanal), heliotropin, hydroxycitronellal, lauraldehyde, lyral (3- and 4- (4-hydroxy-4-methylpentyl) - 3-cyclohexene-1-carboxaldehyde), methylnonylacetaldehyde, lilial (3- (4-tert-butylphenyl) -2-methylpropanal), phenylacetaldehyde, undecylene aldehyde, vanill
  • Perfume compounds of the ketone type are, for example, methyl beta-naphthyl ketone, musk indanone (1,2,3,5,6,7-hexahydro-1,1,2,3,3-pentamethyl-4H-inden-4-one), Tonalid (6-acetyl-1,1,2,4,4,7-hexamethyltetralin), alpha-Damascon, beta-Damascon, delta-Damascon, iso-Damascon, Damascenon, methyldihydrojasmonat, Menthon, Carvon, Kampfer, Koavon (3rd , 4,5,6,6-pentamethylhept-3-en-2-one), fenchone, alpha-ionone, beta-ionone, gamma-methyl-ionone, fleuramone (2-heptylcyclopentanone), dihydrojasmon, cis-jasmon , iso-E-Super (1- (1,2,3,
  • Perfume compounds of the alcohol type are, for example, 10-undecen-1-ol, 2,6-dimethylheptan-2-ol, 2-methyl-butanol, 2-methylpentanol, 2-phenoxyethanol, 2-phenylpropanol, 2-tert-butycyclohexanol, 3,5,5-trimethylcyclohexanol, 3-hexanol, 3-methyl-5-phenyl-pentanol, 3-octanol, 3-phenyl-propanol, 4-heptenol, 4-isopropyl-cyclohexanol, 4-tert-butycyclohexanol, 6 , 8-Dimethyl-2-nona-nol, 6-non-1-ol, 9-decen-1-ol, ⁇ -methylbenzyl alcohol, ⁇ -terpineol, amyl salicylate, benzyl alcohol, benzyl salicylate, ⁇ -terpineol
  • Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate (DMBCA), phenylethyl acetate, Benzyl acetate, ethyl methylphenyl glycinate, allyl cyclohexyl propionate, styrallyl propionate, benzyl salicylate, cyclohexyl salicylate, floramate, melusate and jasmine cyclate.
  • DMBCA dimethylbenzylcarbinylacetate
  • the ethers include, for example, benzyl ethyl ether and ambroxan.
  • the hydrocarbons mainly include terpenes such as limonene and pinene.
  • fragrances are preferably used, which together produce an appealing fragrance.
  • a mixture of fragrances can also be referred to as perfume or perfume oil.
  • perfume oils can also contain natural fragrance mixtures, such as are obtainable from plant sources.
  • the fragrances of plant origin include essential oils such as angelica root oil, anise oil, arnica flower oil, basil oil, bay oil, champaca flower oil, citrus oil, noble fir oil, noble pine cone oil, elemi oil, eucalyptus oil, fennel oil, spruce needle oil, galbanum oil, geranium oil, guan oil oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, ginger oil, guin oil, ginger oil , ginger oil, iris oil, jasmin oil, cajeput oil, calamus
  • the fragrance is used as a fragrance precursor or in encapsulated form (fragrance capsules), in particular in microcapsules.
  • the microcapsules can be water-soluble and / or water-insoluble microcapsules.
  • melamine-urea-formaldehyde microcapsules, melamine-formaldehyde microcapsules, urea-formaldehyde microcapsules or starch microcapsules can be used.
  • “Fragrance precursor” refers to compounds which only release the actual fragrance after chemical conversion / cleavage, typically by exposure to light or other environmental conditions, such as pH, temperature. Such compounds are often also referred to as fragrance storage substances or “pro-fragrance”.
  • the amount of fragrance in the melting bodies is preferably between 0.1 to 20% by weight, preferably 1 to 15% by weight, in particular 3 to 10% by weight, based on the total weight of the composition.
  • the perfume-containing melting body can further comprise at least one textile care compound.
  • a textile-care compound is understood to mean any compound that imparts an advantageous effect to the textile fabrics treated with it, such as, for example, a textile-softening effect, crease resistance or the harmful or negative effects that occur during cleaning and / or conditioning and / or wear, such as fading, graying, etc., is reduced.
  • the textile-care compound may preferably consist of textile softening compounds, bleaching agents, bleach activators, enzymes, silicone oils, antiredeposition agents, optical brighteners, graying inhibitors, shrink preventatives, anticrease agents, dye transfer inhibitors, antimicrobial active ingredients, germicides, fungicides, antioxidants, antistatic agents, ironing aids, waterproofing and Impregnating agents, swelling and anti-slip agents, UV absorbers and mixtures thereof can be selected.
  • the fabric care compound is a fabric softening compound. It is very particularly preferred that the textile-softening compound is selected from polysiloxanes, textile-softening clays, cationic polymers and mixtures thereof.
  • polysiloxanes and / or cationic polymers as a textile care compound in the melting bodies is advantageous since they not only have a softening effect, but also enhance the perfume impression on the laundry.
  • softening clays as a textile-care compound in the composition is advantageous because they additionally have a water-softening effect and, for example, limescale deposits on the laundry can be prevented.
  • a melting body contains a combination of at least two textile care compounds.
  • the melting bodies produced according to the invention contain such textile care compounds, they are used in particular as textile care agents or fabric softeners or as a component of such an agent or also as a component of a detergent.
  • Such a fabric softener can be used in the main wash cycle of an automatic washing or cleaning process.
  • the composition can be added, for example, together with the washing or cleaning agent into the drum or the washing-in chamber of a washing machine. This has the advantage that no additional rinse cycle is necessary and there are no unsightly deposits in the induction chamber
  • such a solid melting body can be used in the washing cycle of a laundry cleaning process and thus transport the textile care compound and the perfume to the laundry right at the beginning of the washing process in order to be able to develop their full potential. Furthermore, this melting body is easier and easier to handle than liquid compositions, since there are no drops left on the edge of the bottle, which during the subsequent storage of the bottle lead to edges on the surface or to unsightly deposits in the area of the closure. The same applies in the event that something is accidentally spilled by the melting body during the dosing. The spilled amount can also be removed more easily and cleanly.
  • Polydimethylpolysiloxanes are known as efficient textile care compounds.
  • Suitable polydimethysiloxanes include DC-200 (ex Dow Corning), Baysilone® M 50, Baysilone® M 100, Baysilone® M 350, Baysilone® M 500, Baysilone® M 1000, Baysilone® M 1500, Baysilone® M 2000 or Baysilone® M 5000 (all ex GE Bayer Silicones).
  • the polysiloxane contains the structural units a) and b).
  • a particularly preferred polysiloxane has the following structure: (CH 3 ) 3 Si- [O-Si (CH 3 ) 2 ] n - [O-Si (CH 3 ) ⁇ (CH 2 ) 3 -NH- (CH 2 ) 2 -NH 2 ⁇ ] x -OSi ( CH 3 ) 3 where the sum n + x is a number between 2 and 10,000.
  • Suitable polysiloxanes with the structural units a) and b) are, for example, commercially available under the brand names DC2-8663, DC2-8035, DC2-8203, DC05-7022 or DC2-8566 (all ex Dow Corning). Also suitable according to the invention are, for example, the commercially available products Dow Corning® 7224, Dow Corning® 929 Cationic Emulsion or Formasil 410 (GE Silicones).
  • a suitable textile softening clay is, for example, a smectite clay.
  • Preferred smectite clays are beidellite clays, hectorite clays, laponite clays, montmorillonite clays, nontronite clays, Saponite clays, Sauconite clays and mixtures thereof.
  • Montmorillonite clays are the preferred softening clays.
  • Bentonites mainly contain montmorillonites and can serve as a preferred source of fabric softening clay. The bentonites can be used as powders or crystals.
  • Suitable bentonites are sold, for example, under the names Laundrosil® by Süd-Chemie or under the name Detercal by Laviosa. It is preferred that the fabric care composition contains a powdered bentonite as the fabric care compound.
  • the melting bodies contain a textile-softening compound and one or more further textile-care compound (s).
  • the amount of textile care compound in the melting body can, in various embodiments, be 0.1 to 15% by weight and preferably 2 to 12% by weight.
  • the melting bodies can optionally contain further ingredients.
  • these additional ingredients are preferably selected from the group consisting of dyes, fillers, polysaccharides, pearlescent agents, skin-care compounds, bitter substances and mixtures thereof.
  • dyes In order to improve the aesthetic impression of the enamel bodies, they can be colored with suitable dyes.
  • Preferred dyes the selection of which is not difficult for the person skilled in the art, should have a high storage stability and insensitivity to the other ingredients of the detergents or cleaning agents and to light, and should not have a pronounced substantivity to textile fibers, in order not to dye them.
  • the melting bodies can contain a filler such as silica or inorganic salts such as sodium sulfate.
  • the amount of filler can be between 0 and 30% by weight and is preferably 1 to 30% by weight.
  • Suitable polysaccharides include, for example, starch.
  • the amount can also be between 0 and 30% by weight and is preferably 1 to 30% by weight.
  • the melting bodies can also contain a pearlescent agent to increase the gloss.
  • suitable pearlescent agents are ethylene glycol mono- and distearate and PEG-3 distearate.
  • the melting body can comprise a skin-care compound.
  • a skin-care compound is understood to mean a compound or a mixture of compounds which, when a textile comes into contact with the detergent, are absorbed onto the textile and give the skin an advantage when the textile comes into contact with skin compared to a textile which is not treated with the composition according to the invention has been.
  • This advantage can include, for example, the transfer of the skin-care compound from the textile to the skin, less water transfer from the skin to the textile or less friction on the skin surface by the textile.
  • the amount of skin-care compound is preferably between 0.01 and 10% by weight, preferably between 0.1 and 5% by weight and very particularly preferably between 0.3 and 3% by weight, based on the total weight of the melting body. It may be that the skin care compound also has a textile care effect.
  • the melting body composition In order to prevent oral absorption of the melting body composition by humans, in particular children, or animals, it can contain a bitter substance such as Bitrex®.
  • the fusible bodies produced by the methods described herein can have any shape.
  • the shaping takes place in particular in step (d) of the described method.
  • Solid, particulate shapes are preferred, such as, for example, essentially spherical, figurative, scaly, cuboid, cylindrical, conical or needle-shaped particles.
  • the particles can have a gummy bear-like, figurative design.
  • the maximum dimension of the particles in a spatial dimension is preferably from 0.5 to 10 mm, in particular 0.8 to 7 mm and particularly preferably 1 to 3 mm. This means that, for example in the case of spherical particles, the diameter of the particles is from 0.5 to 10 mm, in particular 0.8 to 7 mm and particularly preferably 1 to 3 mm.
  • the weight of the individual particles is usually between 2 and 150 mg, preferably between 5 and 10 mg.
  • the generation of a melt, the melting is carried out in step (a) of the methods described herein by heating to a temperature which is not more than 20 ° C. above the melting point of the carrier polymer.
  • Melting can be carried out using all customary methods and devices known to those skilled in the art.
  • the melt that the at least one carrier polymer is produced continuously, for example, by continuously feeding the at least one carrier polymer and possibly further constituents of the melting body to a corresponding device in which it is heated and the melt thus produced is conveyed further, for example pumped.
  • the melt can also be produced separately, for example in a batch process. According to the invention, such embodiments are also included in which the constituents of the melt are mixed with one another at any time before the method according to the invention is carried out and the mixture is stored in molten or cooled solid form until the method is carried out.
  • the at least one fragrance is then metered continuously into the melt.
  • the at least one fragrance is preferably used in liquid form, for example as a perfume oil, solution in a suitable solvent or as a slurry of perfume capsules in a, typically water-containing, solvent.
  • “Liquid” as used in this context means liquid under the conditions of use, preferably liquid at 20 ° C.
  • the flow can optionally be controlled by measuring the flow rate of the individual metering streams, ie the melt, the fragrance stream and, if appropriate, further ingredient streams. This can also be used to set the proportions of the individual components, for example.
  • the ingredients in addition to the carrier polymer (s) and the fragrances can either be produced directly with the carrier polymer as a melt, can be metered in together with the fragrances or separately to the melt. In the latter alternative, the fragrances can be added before or after the fragrances are added.
  • the method according to the invention is characterized in that the at least one textile care compound and / or the additional ingredients (A) are metered into the melt which is optionally produced and promoted in step (a) and / or (B) which contains, optionally produced and promoted, melt produced in step (a).
  • the method according to the invention can be characterized in that the at least one textile care compound and / or the additional ingredients (A) are added to the melt produced and promoted in step (a) and / or (B) in the step ( a) produced and promoted, melt are included.
  • the mixing of the combined metering streams can then take place directly after metering in or downstream after metering in several or all of the ingredients using suitable mixers, such as conventional static or dynamic mixing units.
  • the melt which contains the fragrances and, if appropriate, further ingredients and the carrier polymer, is cooled and optionally fed to the shaping, where the melt solidifies and obtains its final shape.
  • Suitable shaping processes are known to the person skilled in the art. Usual shapes have already been described above.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Fats And Perfumes (AREA)
  • Detergent Compositions (AREA)

Claims (9)

  1. Procédé de production en continu de corps fusibles contenant du parfum, comprenant au moins un polymère de support hydrosoluble ou hydrodispersable ayant un point de fusion > 30 °C à 250 °C, de préférence > 40 °C à 150 °C, choisi de préférence parmi les polyalkylèneglycols, de préférence encore le polyéthylèneglycol, et au moins une matière odorante, caractérisé en ce que le procédé comprend les étapes :
    (a) de transport en continu, éventuellement de génération et de transport en continu, d'une masse fondue comprenant l'au moins un polymère de support hydrosoluble ou hydrodispersable ;
    (b) d'ajout de manière dosée en continu de l'au moins une matière odorante à la masse fondue comprenant l'au moins un polymère de support hydrosoluble ou hydrodispersable ;
    (c) de mélange de la masse fondue comprenant l'au moins un polymère de support hydrosoluble ou hydrodispersable et de l'au moins une matière odorante ; et
    (d) de refroidissement et éventuellement de façonnage du mélange afin d'obtenir des corps fusibles contenant du parfum.
  2. Procédé selon la revendication 1, caractérisé en ce que le polymère de support hydrosoluble
    (A) présente un point de fusion de 48 °C à 120 °C, de préférence de 48 °C à 80 °C ; et/ou
    (B) est contenu dans les corps fusibles en une quantité de 30 à 95 % en poids par rapport au poids total de ceux-ci ; et/ou
    (C) est un polyéthylèneglycol ayant un poids moléculaire moyen > 1 500g/mol, de préférence un poids moléculaire moyen compris entre 3 000 et 15 000, plus préférentiellement un poids moléculaire moyen compris entre 4 000 et 13 000 et plus préférentiellement encore un poids moléculaire moyen compris entre 9 000 et 12 000, et un point de fusion dans la plage de 45 à 70 °C, de préférence de 50 à 65 °C.
  3. Procédé selon la revendication 1 ou 2, caractérisé en ce que l'au moins une matière odorante
    (A) est contenue dans la composition en une quantité de 0,1 à 20 % en poids ; et/ou
    (B) est utilisée sous forme de capsules de matière odorante et/ou d'huiles de parfum.
  4. Procédé selon l'une des revendications 1 à 3, caractérisé en ce que le corps fusible contient en outre au moins un composé d'entretien textile, celui-ci étant choisi de préférence parmi les composés adoucissants textiles, les huiles de silicone, les agents anti-redéposition, les azurants optiques, les inhibiteurs de grisonnement, les agents anti-rétrécissement, les agents anti-froissage, les inhibiteurs de transfert de couleur, les antimicrobiens, les germicides, les fongicides, les antioxydants, les antistatiques, les auxiliaires de repassage, les agents d'étanchéité et d'imprégnation, les agents gonflants et antidérapants, les absorbeurs d'UV ainsi que des mélanges de ceux-ci.
  5. Procédé selon l'une des revendications 1 à 4, caractérisé en ce que le composé d'entretien textile est un composé adoucissant textile, choisi de préférence parmi les polysiloxanes, les argiles adoucissantes textiles, les polymères cationiques et des mélanges de ceux-ci.
  6. Procédé selon l'une des revendications 1 à 5, caractérisé en ce que le corps fusible contient des constituants supplémentaires, choisis de préférence dans le groupe constitué par les colorants, les charges, les nacres, les composés de soin de la peau, les substances amères et des mélanges de ceux-ci.
  7. Procédé selon l'une des revendications 4 à 6, caractérisé en ce que l'au moins un composé d'entretien textile et/ou les constituants supplémentaires (A) sont ajoutés de manière dosée à la masse fondue transportée, éventuellement générée et transportée, à l'étape (a), et/ou (B) sont contenus dans la masse fondue transportée, éventuellement générée et transportée, à l'étape (a).
  8. Procédé selon l'une des revendications 1 à 7, caractérisé en ce que l'écoulement de la masse fondue et/ou de l'au moins une matière odorante est commandé en mesurant le taux d'écoulement des flux de dosage.
  9. Procédé selon l'une des revendications 1 à 8, caractérisé en ce que le mélange à l'étape (c) est effectué avec un mélangeur statique ou dynamique.
EP17771764.2A 2016-09-26 2017-09-22 Procédé de production en continu de corps fusibles contenant du parfum Active EP3516033B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE102016218483 2016-09-26
DE102016219295.7A DE102016219295A1 (de) 2016-09-26 2016-10-05 Kontinuierliches Verfahren zur Herstellung parfümhaltiger Schmelzkörper
PCT/EP2017/074105 WO2018055117A1 (fr) 2016-09-26 2017-09-22 Procédé de production en continu de corps fusibles contenant du parfum

Publications (2)

Publication Number Publication Date
EP3516033A1 EP3516033A1 (fr) 2019-07-31
EP3516033B1 true EP3516033B1 (fr) 2020-08-05

Family

ID=61564513

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17771764.2A Active EP3516033B1 (fr) 2016-09-26 2017-09-22 Procédé de production en continu de corps fusibles contenant du parfum

Country Status (4)

Country Link
US (1) US11001788B2 (fr)
EP (1) EP3516033B1 (fr)
DE (1) DE102016219295A1 (fr)
WO (1) WO2018055117A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112601805B (zh) * 2018-07-09 2022-04-01 宝洁公司 包装的组合物
MX2024008313A (es) 2022-01-30 2024-07-19 The Procter & Gamble Company Metodo de elaboracion de particulas que contienen perfume.

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5328684A (en) 1989-01-17 1994-07-12 Morgan Food Products, Inc. Flavoring, fragance, skin texturizing and deodorant materials and method of making same
EP1627573A1 (fr) 2004-08-20 2006-02-22 Firmenich Sa Procédé pour incorporation d'un ingrédient ou d'une composition de saveur ou de parfum dans une matrice glucidique
WO2008009521A1 (fr) 2006-07-20 2008-01-24 Henkel Ag & Co. Kgaa Procédé de production d'une composition solide d'adoucissant textile
WO2011056938A1 (fr) 2009-11-05 2011-05-12 The Procter & Gamble Company Additif de parfum de lessive
US20120270765A1 (en) 2009-11-05 2012-10-25 Yousef Georges Aouad Laundry scent additive
US8497234B2 (en) 2006-04-06 2013-07-30 Henkel Ag & Co. Kgaa Solid textile care composition comprising a water-soluble polymer
WO2016078942A1 (fr) 2014-11-17 2016-05-26 Unilever Plc Composition de traitement de textile

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102007037147A1 (de) * 2007-08-07 2009-02-12 Henkel Ag & Co. Kgaa Duftkomposite mit verbesserter Duftfreisetzung
CA2960390A1 (fr) * 2014-09-26 2016-03-31 The Procter & Gamble Company Compositions rafraichissantes et dispositifs les comprenant

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5328684A (en) 1989-01-17 1994-07-12 Morgan Food Products, Inc. Flavoring, fragance, skin texturizing and deodorant materials and method of making same
EP1627573A1 (fr) 2004-08-20 2006-02-22 Firmenich Sa Procédé pour incorporation d'un ingrédient ou d'une composition de saveur ou de parfum dans une matrice glucidique
US8497234B2 (en) 2006-04-06 2013-07-30 Henkel Ag & Co. Kgaa Solid textile care composition comprising a water-soluble polymer
WO2008009521A1 (fr) 2006-07-20 2008-01-24 Henkel Ag & Co. Kgaa Procédé de production d'une composition solide d'adoucissant textile
WO2011056938A1 (fr) 2009-11-05 2011-05-12 The Procter & Gamble Company Additif de parfum de lessive
US20120270765A1 (en) 2009-11-05 2012-10-25 Yousef Georges Aouad Laundry scent additive
WO2016078942A1 (fr) 2014-11-17 2016-05-26 Unilever Plc Composition de traitement de textile

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
ANONYMOUS: "AutoBlend System - Continuous Production of Fabric Softener", SPX, 1 March 2013 (2013-03-01), pages 1 - 3, XP055804375, Retrieved from the Internet <URL:https://www.spxflow.com/bran-luebbe/products/autoblend-system-continuous-production-of-fabric-softener/> [retrieved on 20210514]
ANONYMOUS: "AutoBlend System - Continuous Production of Liquid Detergent", SPX, 1 March 2013 (2013-03-01), pages 1 - 3, XP055804374, Retrieved from the Internet <URL:https://www.spxflow.com/bran-luebbe/products/autoblend-system-continuous-production-of-liquid-detergent/> [retrieved on 20210514]
ANONYMOUS: "Maltodextrin - American Chemical Society", ACS, 23 April 2018 (2018-04-23), pages 1 - 3, XP055804371, Retrieved from the Internet <URL:https://www.acs.org/content/acs/en/molecule-of-the-week/archive/m/maltodextrin.html> [retrieved on 20210514]
TERRENCE BLEVINS ET AL: "Control Loop Foundation: Batch and Continuous Processes", HANDBOOK OF INDUSTRIAL MIXING - SCIENCE AND PRACTICE, 2011, pages 12, XP055820830

Also Published As

Publication number Publication date
WO2018055117A1 (fr) 2018-03-29
US20190218480A1 (en) 2019-07-18
US11001788B2 (en) 2021-05-11
EP3516033A1 (fr) 2019-07-31
DE102016219295A1 (de) 2018-03-29

Similar Documents

Publication Publication Date Title
EP3516029B1 (fr) Pastilles parfumées en dispersions de masse fondue contenant des solides
EP3636736B1 (fr) Utilisation des corps moulés sous forme de gel permettant de parfumer des textiles lors du processus de lavage
EP3516030A1 (fr) Compositions sous forme de particules solides comprenant un polymère vecteur soluble dans l&#39;eau et du parfum
EP3476927A1 (fr) Composition de parfum solide
EP3728540B1 (fr) Fabrication de corps fusibles contenant un parfum
EP3701004A1 (fr) Composition solide contenant du parfum
EP3516033B1 (fr) Procédé de production en continu de corps fusibles contenant du parfum
EP3722405A1 (fr) Composition solide contenant du parfum
WO2018055114A1 (fr) Sucre employé comme matière porteuse de parfum
DE102016219294A1 (de) Verfahren zur Herstellung von bitterstoff-haltigen Schmelzkörpern
WO2018055115A1 (fr) Corps fusible contenant un parfum et contenant des tensioactifs non ioniques fortement éthoxylés
DE102017007096A1 (de) Zucker als Duftstoff-Trägermaterial
WO2019081280A1 (fr) Composition solide contenant du parfum
DE102016219570A1 (de) Verarbeitungsfreundliche Masse zur Herstellung von Schmelzkörpern
DE102017203505A1 (de) Parfümhaltige Schmelzkörper enthaltend EO/PO-Block-Copolymere
WO2018055113A1 (fr) Corps fusibles contenant des parfums et comprenant des copolymères séquencés à base d&#39;oxyde d&#39;éthylène/oxyde de propylène
WO2019120714A1 (fr) Fabrication de corps fusibles contenant du parfum
WO2019120779A1 (fr) Fabrication de corps fusibles contenant un parfum
DE102017203502A1 (de) Parfümhaltige Schmelzkörper enthaltend hochethoxylierte, nichtionische Tenside
DE102017218988A1 (de) Feste parfümhaltige Zusammensetzung
WO2018055120A1 (fr) Procédé de fabrication de corps fusibles contenant une substance amère
DE102017222998A1 (de) Herstellungsverfahren für kugelförmige Duftperlen
DE102017218987A1 (de) Feste parfümhaltige Zusammensetzung
EP3360951A1 (fr) Composition comprenant de l&#39;huile de parfum et des capsules de parfum

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: 20190123

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)
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: 20200331

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

Free format text: NOT ENGLISH

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1298730

Country of ref document: AT

Kind code of ref document: T

Effective date: 20200815

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 502017006637

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: GERMAN

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20200805

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

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: 20200805

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: 20200805

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: 20201106

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: 20200805

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: 20200805

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: 20201207

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: 20200805

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: 20201105

Ref country code: BG

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: 20201105

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

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: 20200805

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: 20200805

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: 20200805

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: 20200805

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: 20201205

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 502017006637

Country of ref document: DE

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: 20200805

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: 20200805

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: 20200805

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: 20200805

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: 20200805

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

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: 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: 20200805

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: 20200805

26 Opposition filed

Opponent name: UNILEVER IP HOLDINGS B.V./ UNILEVER GLOBAL IP LIMITED

Effective date: 20210429

Opponent name: THE PROCTER & GAMBLE COMPANY

Effective date: 20210505

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20200930

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: 20200805

Ref country code: LU

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

Effective date: 20200922

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

Ref country code: IT

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: 20200805

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

Ref country code: CH

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

Effective date: 20200930

Ref country code: BE

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

Effective date: 20200930

Ref country code: IE

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

Effective date: 20200922

Ref country code: LI

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

Effective date: 20200930

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: 20200805

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

Free format text: ORIGINAL CODE: EPIDOSNOBS3

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

Ref country code: TR

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: 20200805

Ref country code: MT

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: 20200805

Ref country code: CY

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: 20200805

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

Ref country code: MK

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: 20200805

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

R26 Opposition filed (corrected)

Opponent name: THE PROCTER & GAMBLE COMPANY

Effective date: 20210505

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

R26 Opposition filed (corrected)

Opponent name: UNILEVER IP HOLDINGS B.V./ UNILEVER GLOBAL IP LIMITED

Effective date: 20210429

RDAF Communication despatched that patent is revoked

Free format text: ORIGINAL CODE: EPIDOSNREV1

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

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

Effective date: 20230530

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

REG Reference to a national code

Ref country code: AT

Ref legal event code: MM01

Ref document number: 1298730

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220922

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

Ref country code: AT

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

Effective date: 20220922

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

R26 Opposition filed (corrected)

Opponent name: UNILEVER IP HOLDINGS B.V./ UNILEVERGLOBAL IP LIMITED

Effective date: 20210429

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

Ref country code: DE

Payment date: 20240918

Year of fee payment: 8

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

Ref country code: GB

Payment date: 20240920

Year of fee payment: 8

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

Ref country code: FR

Payment date: 20240925

Year of fee payment: 8