[go: up one dir, main page]

EP1358311B1 - Compositions de nettoyage - Google Patents

Compositions de nettoyage Download PDF

Info

Publication number
EP1358311B1
EP1358311B1 EP02716699A EP02716699A EP1358311B1 EP 1358311 B1 EP1358311 B1 EP 1358311B1 EP 02716699 A EP02716699 A EP 02716699A EP 02716699 A EP02716699 A EP 02716699A EP 1358311 B1 EP1358311 B1 EP 1358311B1
Authority
EP
European Patent Office
Prior art keywords
water
tablet
weight
zeolite
disintegrant
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.)
Expired - Lifetime
Application number
EP02716699A
Other languages
German (de)
English (en)
Other versions
EP1358311A1 (fr
Inventor
Jelles V. Unilever R & D Vlaardingen BOSKAMP
Ian Unilever R & D Vlaardingen CALLAGHAN
Somdath Unilever R & D Vlaardingen CHOENNIE
Paulus J. M. Unilever R & D Vlaardingen LOOMANS
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 PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Priority to EP02716699A priority Critical patent/EP1358311B1/fr
Publication of EP1358311A1 publication Critical patent/EP1358311A1/fr
Application granted granted Critical
Publication of EP1358311B1 publication Critical patent/EP1358311B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0065Solid detergents containing builders
    • C11D17/0073Tablets
    • 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
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0065Solid detergents containing builders
    • C11D17/0073Tablets
    • C11D17/0078Multilayered tablets
    • 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
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
    • 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

Definitions

  • the present invention relates to cleaning compositions in the form of tablets. These tablets are intended to disintegrate when placed in water and thus are intended to be consumed in a single use.
  • the tablets may be suitable for use in machine dishwashing, the washing of fabrics or other cleaning tasks.
  • Products in tablet form have several advantages over powdered products: for example, they do not require measuring and are thus easier to handle and dispense into the wash-load, and they are more compact, hence facilitating more economical storage.
  • compositions in tablet form and intended for fabric washing have been described in a number of patent documents including, for example WO-98/42817 and WO-99/20730 (all Unilever), and are now sold commercially. Tablets of composition suitable for machine dishwashing have been disclosed in WO-96/23530 and US-A-5691293 and are sold commercially.
  • Tablets of a cleaning composition are generally made by compressing or compacting a composition in particulate form. Although it is desirable that tablets have adequate strength when dry, yet disperse and dissolve quickly when brought into contact with water, it can be difficult to obtain both properties together. Tablets formed using a low compaction pressure tend to crumble and disintegrate on handling and packing; while more forcefully compacted tablets may be sufficiently cohesive but then fail to disintegrate or disperse to an adequate extent in the wash. Tabletting will often be carried out with enough pressure to achieve a compromise between these desirable but antagonistic properties. However, it remains desirable to improve one or other of these properties without detriment to the other so as to improve the overall compromise between them. US-A-3018267 (Procter & Gamble) taught that the force, and hence pressure, applied when compacting a composition into tablets should be limited, or else the tablets would take too long to dissolve.
  • a tablet contains organic surfactant, this can function as a binder, plasticising the tablet. However, it can also retard disintegration of the tablet by forming a viscous gel when the tablet comes into contact with water. Thus, the presence of surfactant can make it more difficult to achieve both good strength and speed of disintegration: the problem has proved especially acute with tablets formed by compressing powders containing surfactant and built with insoluble detergency builder such as sodium aluminosilicate (zeolite) .
  • insoluble detergency builder such as sodium aluminosilicate (zeolite)
  • EP-A-711 827 (Unilever ) teaches the use of sodium citrate for this purpose and EP-A-838519 (Unilever) teach the use of sodium acetate trihydrate for this purpose.
  • Typical water-swellable agents which have been disclosed as possible tablet disintegrating agents are starches, cellulose and cellulose derivatives, alginates, dextrans, cross-linked polyvinyl pyrrolidones, gelatines and formaldehyde casein as well as a wide variety of clay minerals and certain ion-exchange resins.
  • these water swellable agents have no function in fabric washing except to aid tablet disintegration. Furthermore, because they are insoluble and of relatively large particle size, they tend to deposit on fabric during the wash; see for example WO-98/55575 (Henkel ). As a result, several attempts have been made to minimise the deposition of these disintegrants, for example by combining such a water swellable water soluble disintegrant with a second, highly soluble disintegration aid (see WO-98/55582 and WO-98/55590 both Unilever). Other attempts have included use of a preferred particle size of the disintegrant.
  • WO-98/55583 (Unilever ) discloses the use of such materials at a particle dimension of at least 400um to give more efficient disintegration.
  • WO-98/55575 (Henkel ) however teaches the use of cellulose disintegrating aids with a particle size of less than 100 um in order to minimise deposition.
  • the cellulose material is mixed with a material of a given oil absorbing capacity, which includes some zeolites.
  • a water swellable disintegrating aid is co-granulated with a water-insoluble inorganic material before being incorporated into a tablet, and, the disintegrant granule is used in a tablet comprising certain water-soluble disintegration-promoting particles, or, an aluminosilicate builder and an enzyme, then the disintegration granule is more effective. Less of the disintegrating aid then needs to be used for effective disintegration of the tablet in turn lowering the probability of deposition of the disintegrating aid on the substrate being cleaned.
  • the present invention provides a tablet of compacted particulate detergent composition comprising non-soap surfactant and detergency builder, wherein the tablet or a discrete region thereof comprises; a tablet according to claim 1.
  • the present invention provides a tablet of compacted particulate detergent composition according to claim 6
  • a process for making the above tablets comprises mixing compacted disintegrant co-granules with either water-soluble disintegration-promoting particles or with aluminosilicate builder material and one or more detergency enzymes, and with other constituents of the composition to produce a particulate composition, placing a quantity of the resultant particulate composition within a mould and compacting the composition within the mould to produce the tablet.
  • a tablet of the present invention may be either homogeneous or heterogeneous.
  • the term “homogeneous” is used to mean a tablet produced by compaction of a single particulate composition, but does not imply that all the particles of that composition will be of identical composition.
  • the term “heterogeneous” is used to mean a tablet consisting of a plurality of discrete regions, for example layers, inserts or coatings, each derived by compaction from a particulate composition.
  • each discrete region of the tablet will preferably have a mass of at least 5 grams.
  • a tablet according to the invention comprises non-soap surfactant, detergency builder and a disintegrant in the form of compacted co-granules, said disintegrant comprising a water-insoluble inorganic material in the form of a zeolite and a water-swellable agent with a specific water swelling capacity which in its anhydrous state comprises no more than 20% by weight of the combined weight of said inorganic material and said water-swellable agent of the granular disintegrant.
  • water-insoluble in relation to the zeolite material, is meant a zeolite with a solubility in water at 25°C of less than 5 grams per 100 grams of water, preferably less than 1 gram per 100 grams of water.
  • zeolites are zeolites P,A,X or Y or mixtures thereof, with Zeolite P being preferred.
  • a type of Zeolite P, maximum aluminium zeolite P, known as zeolite MAP and so referred to herein e.g. DOUCIL A24 ex Ineos Silicas UK
  • DOUCIL A24 ex Ineos Silicas UK has been found to be especially effective.
  • the preferred amount of water in the zeolite depends upon the type of zeolite used. For zeolites A and P, it is preferred that the amount of water is less than 21% by weight of the zeolite, more preferably less than 15% by weight, especially 8 to 13% by weight. Zeolite MAP, contains from about 9 to about 12% by weight of water and is especially useful according to the present invention.
  • zeolite P we have found that good results are obtained from the partially hydrated material, e.g. zeolite MAP. As the water content in zeolite P is increased above this range (12% by weight for zeolite MAP), the effectiveness as a disintegrant decreases with increasing water content. Fully hydrated zeolite P (denoted "DOUCIL" A28 in the examples herein) has been found to be less effective as a disintegrant when compared to zeolite MAP.
  • Alkali metal aluminosilicates are used in detergent compositions as builders as further described hereinbelow.
  • a composition according to the invention comprises a zeolite as a detergency builder, it is preferred that at least a part of the zeolite in the cleaning composition is employed as component in the formation of the disintegrant co-granules.
  • the builder e.g. zeolite, typically comprises 10 to 60% by weight of the total composition.
  • the zeolite is used in the disintegrant co-granules and as part of the detergency builder in the composition, in that instance at least 1% by weight of the total weight of the composition comprises a zeolite constituent employed in the form of disintegrant co-granules.
  • the water-swellable agent preferably comprises, in its anhydrous state, no more than 15% by weight, preferably no more than 10% by weight, of the combined weight of said zeolite as inorganic material and said water-swellable agent of the granular co-disintegrant.
  • the water-swellable agent comprises, in its anhydrous state, no more than 8% by weight, e.g. 7.5% or less of the combined weight of said inorganic material and said agent.
  • at least 1% of the combined weight of said inorganic material and said water-swellable agent in the granules comprises water-swellable agent. It is preferred that the water swellable agent comprises in its anhydrous state 1 to 15% by weight of the combined weight of said inorganic material and said water-swellable agent.
  • a relatively small amount of the water-swellable agent may, surprisingly, be used in the tabletted composition of the invention whilst still providing an acceptable effect.
  • the amount of water-swellable agent, based on the total weight of the tabletted composition is less than 2% by weight, preferably less than 1% of the composition.
  • at least 0.2% by weight of the water-swellable agent is present in the tabletted composition.
  • the water-swellable agent comprises polymer, often a wholly or partially cross-linked polymer, e.g. natural cellulose, cross-linked cellulose, (sodium) carboxymethyl cellulose, cross-linked sodium carboxymethyl cellulose, pre-gelatinised starch, cross-linked starch or cross-linked polyvinyl pyrrolidone.
  • polymer often a wholly or partially cross-linked polymer, e.g. natural cellulose, cross-linked cellulose, (sodium) carboxymethyl cellulose, cross-linked sodium carboxymethyl cellulose, pre-gelatinised starch, cross-linked starch or cross-linked polyvinyl pyrrolidone.
  • Aquasorb A500 ex Hercules
  • Ac-Di-Sol and Nilyn XL90 ex FMC Corporation, USA.
  • the water swellable agent in the disintegrant granule is preferably a cross-linked carboxymethyl cellulose, such as Aquasorb A500, Ac-Di-Sol and Nilyn as mentioned above. It is believed that these cross-linked carboxymethyl celluloses have particularly suitable levels of crosslinking and/or degree of substitution for use in the present invention.
  • compositions of the invention will contain from 1% to 20% by weight of the compacted disintegrant co-granules based on the total weight of the compositions, preferably 2 to 15%, more preferably 3 to 10%, e.g. 4 to 8% by weight. If the co-granules are included to aid dissolution only of the tablets rather than disintegration, then the amount of the granules in the tablets could be as low as 1% by weight.
  • the water-swellable agent preferably has an average primary particle size up to about 600um, but, conveniently, has an average primary particle size of no more than 200 um, preferably no more than 100um.
  • the compacted disintegrant co-granules have a mean particle size in the range 700 to 1200 micrometers.
  • the water swellable agent has a water-swelling capacity of at least 5 cm 3 /gram, preferably at least 10cm 3 /gram and more preferably at least 20cm 3 /gram as determined in the test described hereinbelow.
  • the compacted disintegrant co-granules comprising the zeolite and the water-swellable agent may be prepared by any of the methods that will be known to those skilled in the art, e.g. by blending the dry ingredients in a mixer (such as a Pek mixer available from George Tweedy & Co of Preston - 281b S.A. Machine) and compacting on a roller compactor (Alexanderwerk WP50 - manufactured by Alexanderwerk AG, D 5630 Rem Kunststoff 1, Germany).
  • a mixer such as a Pek mixer available from George Tweedy & Co of Preston - 281b S.A. Machine
  • a roller compactor Alexanderwerk WP50 - manufactured by Alexanderwerk AG, D 5630 Rem Kunststoff 1, Germany
  • Inorganic material and the water-swellable agent are blended together in appropriate portions, in a Pek mixer for 30 minutes.
  • a minimum of 2 kg of blended material so prepared is compacted by feeding into an Alexanderwerk roller compactor, fitted with a sintered block vacuum deaeration system.
  • the roller pressure is selected according to the strength of granule desired, higher pressures leading to stronger granules. Generally, roller pressure is between 8 and 25 Mpa and a typical roller pressure is 10 Mpa.
  • the compacted material from the compactor is fed into a granulator, which forms part of the machine, and forced through a mesh and the resulting granules are then screened to the desired particle size range, e.g.
  • the granules comprise an intimate mixture of particles of water insoluble inorganic material and water-swellable agent.
  • compositions of this invention contain one or more non-soap surfactants.
  • these preferably provide from 5 to 50% by weight of the composition of the tablet or region thereof, more preferably from 8 or 9% by weight of the composition up to 35% or 40% by weight. If the tablet is composed of more than one discrete region, then these preferred amounts of surfactant may apply to the tablet as a whole.
  • the organic surfactant may be present as a component in granulated particles in an amount between 10 and 70% by weight of the particles, more preferably 15 to 50% by weight based on the total weight of the granulated particles. All the surfactant in the composition may be contained within these particles.
  • the surfactant may be anionic (soap or non-soap), cationic, zwitterionic, amphoteric, nonionic or a combination of these.
  • anionic surfactant may be present in an amount from 0.5 to 50% by weight, preferably from 2% or 4% up to 30% or 35% or 40% by weight of the tablet or region thereof.
  • organic surfactant is likely to constitute from 0.5 to 8%, more likely from 0.5 to 5% of the composition of the tablet or region thereof and is likely to consist of nonionic surfactant, either alone or in a mixture with anionic surfactant.
  • Synthetic (i.e. non-soap) anionic surfactants are well known to those skilled in the art. Examples include alkyl benzene sulphonates, particularly sodium linear alkyl benzene sulphonates having an alkyl chain length of C 8 -C 15 ; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates.
  • soaps of fatty acids are preferably sodium soaps derived from naturally occurring fatty acids, for example, the fatty acids from coconut oil, beef tallow, sunflower or hardened rape seed oil.
  • Suitable nonionic surfactant compounds which may be used include in particular the reaction products of compounds having a hydrophobic group and a reactive hydrogen atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene oxides, especially ethylene oxide.
  • the amount of nonionic surfactant lies in a range from 4 to 40%, better 4 or 5 to 30% by weight of the composition of the tablet or region thereof.
  • Many nonionic surfactants are liquids. These may be absorbed onto particles of the composition prior to compaction into tablets.
  • Amphoteric surfactants may be used jointly with anionic or nonionic surfactants or both cationic surfactants may possibly be used. These frequently have a quaternised nitrogen atom in a polar head group and an attached hydrocarbon group of sufficient length to be hydrophobic.
  • the amount of amphoteric surfactant, if any, may possibly be from 3% to 20 or 30% by weight of the tablet or region of a tablet; the amount of cationic surfactant, if any, may possibly be from 1% to 10 or 20% by weight of the tablet or region of a tablet.
  • a composition which is compacted to form tablets or tablet regions typically contains a detergency builder which serves to remove or sequester calcium and/or magnesium ions in the water.
  • the builder acts as a water softener.
  • the amount of builder is likely to be from 5% to 80%, more usually 10% or 15% to 40%, 55% or 60% by weight of the tablet.
  • the detergency builder may be present in granulated particles in an amount of from 20 to 80% by weight, more preferably 20%, 25% or 30 to 60% by weight.
  • Detergency builders may be provided wholly by water soluble materials, or may be provided in large part or even entirely by water-insoluble material with water-softening properties.
  • Alkali metal aluminosilicates are strongly favoured as environmentally acceptable detergency builders for fabric washing, and are preferred in this invention.
  • Alkali metal (preferably sodium) aluminosilicates may be either crystalline or amorphous or mixtures thereof.
  • the less preferred category of water-soluble phosphorus-containing inorganic softeners includes the alkali-metal orthophosphates, metaphosphates, pyrophosphates and polyphosphates.
  • Specific examples of inorganic phosphate detergency builders include sodium and potassium tripolyphosphates, orthophosphates and hexametaphosphates.
  • Non-phosphorus water-soluble detergency builders may be organic or inorganic.
  • Inorganics that may be present include alkali metal (generally sodium) carbonate; while organics include polycarboxylate polymers, such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphonates, monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono- di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymalonates, dipicolinates and hydroxyethyliminodiacetates.
  • alkali metal generally sodium
  • organics include polycarboxylate polymers, such as polyacrylates, acrylic/maleic copolymers, and acrylic phosphonates, monomeric polycarboxylates such as citrates, gluconates, oxydisuccinates, glycerol mono- di- and trisuccinates, carboxymethyloxysuccinates, carboxymethyloxymal
  • Tablet compositions preferably include polycarboxylate polymers, more especially polyacrylates and acrylic/maleic copolymers which have some function as water-softening agents and also inhibit unwanted deposition onto fabric from the wash liquor.
  • the tablet contains water soluble builder it is preferably present in an amount of from 10 to 80% by weight based on the total weight of the tablet or region thereof. Where the tablet contains water in-soluble builder it is preferably present in an amount of from 5 to 80% by weight based on the total weight of the tablet or region thereof.
  • Tablets comprising from 4 to 50% by weight of surfactant and from 5 to 80% by weight of builder are especially preferred for fabric washing tablets. Tablets comprising from 1 to 5% by weight of surfactant and from 50 to 98% of detergency builder are especially preferred for machine dishwashing tablets.
  • the percentage ranges for the components referred to herein may apply to the overall composition of the tablet, as well as to at least one region of the tablet.
  • the compositions of the invention in either the whole tablet or in a region thereof, contain water-soluble disintegration promoting particles in addition to the disintegrant granules. These particles may also be present according to the second aspect of the invention. It is preferred that such disintegration-promoting particles make up from 2%, 3%, 5%, 8% or 10% up to 15%, 20%, 25% or 30% by weight of the composition of the tablet or region thereof. It is especially preferred that such disintegration-promoting particles make up from 5% to 25% by weight of the composition, based on the total weight of the composition.
  • Such soluble particles typically contain at least 40% (of their own weight) of one or more materials which is other than soap or organic surfactant and which has a solubility in deionised water of at least 50g/100g at 20°C.
  • at least a part of the water-soluble disintegration-promoting particles is added to a pregranulated portion of the composition which may contain organic surfactant and/or detergency builder used to produce the tablet.
  • a proportion of such soluble material may also be included in granulated particles, in an amount of preferably 1 to 25% by weight, more preferably 3 or 5% to 10% or 15% by weight of these granulated particles.
  • this water-soluble material is selected from compounds containing at least 40% (by weight of the particles) of one or more materials selected from the group consisting of; compounds with a water-solubility exceeding 50 grams/100 grams in water at 20°C; or sodium tripolyphosphate containing at least 50% of its own weight of the phase I anhydrous form; or sodium tripolyphosphate which is partially hydrated so as to contain water of hydration in an amount which is at least 0.5% by weight of the sodium tripolyphosphate in the particles.
  • these disintegration-promoting particles can also contain other forms of tripolyphosphate or other salts within the balance of their composition.
  • the material in such water-soluble disintegration-promoting particles can function as a detergency builder, (as is the case with sodium tripolyphosphate) then of course it contributes to the total quantity of detergency builder in the tablet composition.
  • a solubility of at least 50 g/100g of deionised water at 20°C is an exceptionally high solubility: many materials which are classified as water soluble are less soluble than this.
  • solubilities of some other common materials at 20°C are:- Material Water Solubility (g/100g) Sodium chloride 36 Sodium sulphate decahydrate 21.5 Sodium carbonate anhydrous 8.0 Sodium percarbonate anhydrous 12 Sodium perborate anhydrous 3.7 Sodium tripolyphosphate anhydrous 15
  • this highly water soluble material is incorporated as particles of the material in a substantially pure form (i.e. each such particle contains over 95% by weight of the material).
  • the said particles may contain material of such solubility in a mixture with other material, provided that material of the specified solubility provides at least 50% by weight of these particles.
  • Preferred water-soluble materials having a solubility exceeding 50 grams/100 grams of deionised water at 20°C are sodium citrate dihydrate, urea, and sodium acetate.
  • the sodium acetate may be in a partially or fully hydrated form (trihydrate). Sodium acetate trihydrate is especially preferred.
  • the highly water-soluble material is a salt which dissolves in water in an ionised form. As such a salt dissolves it leads to a transient local increase in ionic strength which can assist disintegration of the tablet by preventing nonionic surfactant from swelling and inhibiting dissolution of other materials.
  • tablets of this invention may contain water-soluble salt, with a solubility exceeding 50g/100g of deionised water at 20°C, both as a small percentage within the said granulated particles and as separate particles which are mixed with them.
  • such highly water soluble salt may be present in an amount of from 0 to 30% by weight of those particles, preferably of from 3 to 10% or 15% thereof, while the materials added to those particles before tabletting may be such highly soluble salts in an amount of from 2 or 5% up to 15% by weight of the whole tablet formulation.
  • the said particles which promote disintegration are particles which contain sodium tripolyphosphate with more than 50% (by weight of the particles) of the anhydrous phase I form, and, which is partially hydrated so as to contain water of hydration in an amount which is at least 1% by weight of the sodium tripolyphosphate.
  • Sodium tripolyphosphate is very well known as a sequestering builder in detergent compositions. It exists in a hydrated form and two crystalline anhydrous forms. These are the normal crystalline anhydrous form, known as phase II which is the low temperature form, and phase I which is stable at high temperature.
  • the remainder of the tablet composition used to form the tablet or region thereof may include additional sodium tripolyphosphate.
  • This may be in any form, including sodium tripolyphosphate with a high content of the anhydrous phase II form. Suitable material is commercially available. Suppliers include Rhone-Poulenc, France and Rhodia, UK.
  • a zero-phosphate tablet in accordance with this invention may utilise a suitable amount, e.g. 15% by weight or more of disintegration-promoting material with solubility of at least 50gm/100gm at 20°C.
  • suitable amount e.g. 15% by weight or more of disintegration-promoting material with solubility of at least 50gm/100gm at 20°C.
  • Other countries permit the use, or at least some limited use, of phosphates, making it possible to use some sodium tripolyphosphate.
  • Tablets of the present invention may include a water-soluble organic polymer which is solid at 25°C to act as a binder for the particulate composition when compacted. This may be included in granulated particles containing organic surfactant and/or detergency builder.
  • Tabletted compositions according to the invention may contain a bleach system.
  • This preferably comprises one or more peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, which may be employed in conjunction with activators to improve bleaching action at low wash temperatures. If any peroxygen compound is present, the amount is likely to lie in a range from 10 to 25% by weight of the composition of the tablet or region thereof.
  • Tablets according to the second aspect of the invention comprise one or more detergency enzymes.
  • the enzyme is selected from amylase, protease, cellulase, lipase and mixtures thereof.
  • the aforementioned enzymes are designed to remove a variety of soils and stains from fabrics.
  • Detergent tablets according to the first aspect of the invention may also comprise one or more detergency enzymes.
  • the tablets of the invention may also contain a fluorescer, an antifoam material in an amount up to 5% by weight of the composition of the tablet or region thereof, an alkali metal silicate, particularly sodium ortho-, meta- or disilicate in providing protection against the corrosion of metal parts in washing machines.
  • the starting particulate composition from which the tablets are produced may in principle have any bulk density
  • the present invention may be especially relevant to tablets of detergent composition made by compacting powders of relatively high bulk density, because of their greater tendency to exhibit disintegration and dispersion problems.
  • Such tablets have the advantage that, compared with a tablet derived from a low bulk density powder, a given dose of composition can be presented as a smaller tablet.
  • the starting particulate composition may suitably have a bulk density of at least 400 g/litre, preferably at least 500 g/litre, and possibly at least 600 g/litre.
  • Granular detergent compositions of high bulk density prepared by granulation and densification in a high-speed mixer/granulator, as described and claimed in EP-A-340 013 (Unilever ), EP-A-352 135 (Unilever ), and EP-A-425 277 (Unilever ), or by the continuous granulation/densification processes described and claimed in EP-A-367 339 (Unilever ) and EP-A-390 251 (Unilever ), are inherently suitable for use in the present invention.
  • WO-A-98/11193 Another particularly suitable process for the preparation of a high-bulk density detergent powder is described in WO-A-98/11193 (Unilever ).
  • a feedstock of the starting acid for production of the anionic surfactant is partially neutralised, for example by sodium hydroxide, before being fed into a high-speed mixer densifier (e.g. Lodige CB 30 Recycler) where the partially neutralised acid feedstock is completely neutralised, whilst being mixed with the majority of other components of the detergent base powder granule.
  • This powder can be further densified by treating in a moderate speed mixer (e.g. Lodige KM 300 mixer), before which stage further detergency builder may be added.
  • a moderate speed mixer e.g. Lodige KM 300 mixer
  • the water-soluble polymer material is preferably added before the further densification step, although it may be added in the first mixer.
  • the water-soluble polymer material may be heated to a temperature considerably above its melting point to obtain a free-flowing liquid.
  • the resulting powder can be cooled and dried using a fluid bed, after which any desired particle size control can be exercised.
  • any separate particles containing further components of the finished formulation can be mixed with the base powder prior to compaction.
  • Particle sizes can be controlled in the manufacturing process of any particles included in the composition. Oversize particles are usually removed by sieving (for example by a Mogensen screen) at the end of the production process, followed by milling and recycling of the removed oversize fraction. Undersize particles can also be removed by sieving, or if the manufacturing process employs a fluidised bed then undersized particles may be entrained in the air stream and subsequently recovered from it for recycling to the granulation stage.
  • the average particle size of granulated particles forming the particulate composition from which,the tablet is formed is between 400 and 1100 micrometers, preferably between 500 and 1000 micrometers. Preferably no more than 5% of these particles are smaller than 200 micrometers while no more than 5% are larger than 1400 micrometers.
  • Materials which are mixed with the granulated particles may also comply with these requirements concerning particle size. These materials (post-added) typically comprise from 5% - 60% by weight of the total weight of the final composition, more usually 35 to 55% by weight.
  • Tabletting entails compaction of a particulate composition.
  • tabletting machinery is known, and can be used. Generally it will function by stamping a quantity of the particulate composition which is confined in a die. Tabletting may be carried out at ambient temperature or at a temperature above ambient which may allow adequate strength to be achieved with less applied pressure during compaction.
  • the particulate composition is preferably supplied to the tabletting machinery at an elevated temperature. This will of course supply heat to the tabletting machinery, but the machinery may be heated in some other way also. If any heat is supplied, it is envisaged that this will be supplied conventionally, such as by passing the particulate composition through an oven, rather than by any application of microwave energy.
  • the size of a tablet will suitably range from 10 to 160 grams, preferably from 15 to 60 grams, depending on the conditions of intended use, and whether it represents a dose for an average load in a fabric washing or dishwashing machine or a fractional part of such a dose.
  • the tablets may be of any shape. However, for ease of packaging they are preferably blocks of substantially uniform cross-section, such as cylinders or cuboids.
  • the overall density of a tablet for fabric washing preferably lies in a range from 1040 or 1050g/litre preferably at least 1100g/litre up to 1400g/litre.
  • the tablet density may well lie in a range up to no more than 1350 or even 1250g/litre.
  • the overall density of a tablet of some other cleaning composition such as a tablet for machine dishwashing or as a bleaching additive, may range up to 1700g/litre and will often lie in a range from 1300 to 1550g/litre.
  • the detergent tablet may be made by a process which comprises mixing the compacted disintegrant co-granules with either the water-soluble disintegration-promoting particles or with the aluminosilicate builder material and one or more detergency enzymes, and with the other constituents of the composition, placing a quantity of the resultant particulate composition within a mould and compacting the composition within the mould to produce the tablet.
  • the speed of disintegration of the tablets in the examples was measured by means of a test procedure under static conditions in which a pre-weighed tablet was placed on a metal grid with 1 X 1 cm mazes and the tablet and grid was then immersed in a suitable amount of 15° FH (French Hardness) tap water at 10°C or 20°C so that the tablet when immersed is covered by 2cm of water. After 60 seconds the metal grid is carefully taken out of the water and the wet tablet residue is weighed. If the tablet had fully disintegrated in this time then the time taken for 100% disintegration is recorded.
  • FH Frnch Hardness
  • the tablets exhibit 50% or more disintegration in the above test, more preferably 60% or more, most preferably 70% or more.
  • DFS diametrical fracture stress in Pascals
  • F max the applied load in Newtons to cause fracture
  • D is the tablet diameter in metres
  • t is the tablet thickness in metres.
  • the test is carried out using an Instron type universal testing instrument to apply compressive force on a tablet diameter (i.e. perpendicular to the axis of a cylindrical tablet). It is preferred that tablets have a DFS of at least 20 kPa more preferably at least 25 kPa, such as 30 kPa or above.
  • the tablets when used as fabric washing tablets in an automatic washing machine, may be added either to the powder dispensing draw, or, directly in to the washing drum. This may occur either manually or automatically.
  • the detergent/cleaning tablets of the invention are suitable for use in what is known in the art as 'homecare' applications. That is, detergent tablets which are suitable for use in cleaning and maintainance operations typically carried out around the home. It does not include operations carried out directly on a human or animal body which are known as 'personal care' applications.
  • 'homecare' detergent tablets include; laundry tablets, (machine) dishwashing tablets, hard-surface cleaning tablets, toilet-cleaning tablets, bleaching tablets, water-softening tablets etc.
  • disintegrant granules were prepared by the typical preparative method described under the heading "Disintegrant granules".
  • the disintegrant granules used either a zeolite or silica as the water-insoluble inorganic material.
  • the water-swellable agent was chosen from one of four types of water-swellable agents.
  • the granules had the compositions given in table 2 and were sieved to collect the fraction having a particle size of 250 to 700um or 700 to 1200 um. Unless otherwise stated the particle size is or 700 to 1200 um.
  • the amounts given in Table 2 are the percentages of each ingredient in the disintegrant granule and add up to 100% by weight based on the total weight of the granule.
  • the 'stock 1' composition of table 1 was mixed with additional sodium acetate trihydrate/zeolite blend (99:1 parts by weight) as shown in table 3 to produce comparative examples C1 and C2.
  • Comparative example C1 contains no disintegrant granule.
  • Comparative example C2 also contains no disintegrant granule but contains Aquasorb A500 cross-linked CMC added as a separate ingredient as well as some additional zeolite powder.
  • the amounts in Table 3 add up to 100% by weight.
  • each comparative composition 40g portions of each comparative composition were made into cylindrical tablets of 44.5 mm diameter and height 18-22 mm using a Graseby Specac laboratory tabletting machine.
  • the compaction pressure used for each tablet was adjusted so that the tablets were all compacted to the same diametrical fracture stress of 30 kPa.
  • the strength of the tablets, in their dry state as made on the press, was determined as their diametrical fracture stress DFS by the method detailed in the description of the invention above.
  • Table 1 The 'stock 1' composition of table 1 was mixed with varying amounts of disintegrant granule and in some examples additional sodium acetate trihydrate/zeolite blend (99:1 parts by weight) as shown in table 4 to produce examples 1 to 11 which are examples according to the invention.
  • the amounts in Table 4 add up to 100% by weight.
  • a to E below refer to the disintegrant granule for which details are given above.
  • compositions were compacted on a Graseby Laboratory Tablet Press as detailed above for comparative examples C1 and C2 above.
  • Example 3 shows improved disintegration over comparative example C1 (which comprises no disintegrant granule and no acetate). This is observed for both the smaller and larger disintegrant granule particle sizes (compare examples 3 & 7 and 4 & 8). By increasing the particle size of the disintegrant granule, the disintegration result can be improved (compare examples 3 and 4).
  • Examples 9 to 11 show that the following water-swellable polymers are effective as part of the disintegrant granule in the descending order; Ac-Di-Sol > Arbocel FT40 > National Starch 78-1551. This demonstrates that the cross-linked CMC disintegrants are more effective than the pre-gelatinised starch. Comparative example C1 demonstrates that in the absence of either a swellable polymer or the disintegrant granule the tablet does not disintegrate but instead takes in water. Comparative example C2 demonstrates that limited disintegration is achieved when the inorganic carrier and swellable polymer are added in a non-granulated form.
  • the 'stock 2' composition of table 1 was mixed with additional sodium acetate trihydrate/zeolite blend (99:1 parts by weight) as shown in table 6 to produce comparative example C3.
  • the 'stock 2' composition of table 1 was mixed with varying amounts of disintegrant granule and in some examples additional sodium acetate trihydrate/zeolite blend (99:1 parts by weight) and/or PEG 1500 powder as shown in table 7 to produce examples 12 to 19 which are examples according to the invention.
  • the amounts in Table 7 add up to 100% by weight.
  • C to G in the table refers to the disintegrant granule.
  • compositions were compacted on a Graseby Laboratory Tablet Press as detailed above for comparative examples C1 and C2 above.
  • Example 13 demonstrates that fully hydrating the zeolite* 1 (as used in disintegrant granules A and C-E) results in lower disintegration values.
  • Example 14 demonstrates that the zeolite known as Zeolite A4 is also not as effective as the zeolite* 1 as a carrier. Examples 17 to 19 show good results for high levels of the disintegrant granule in the absence of post-added acetate. Comparative example C3 demonstrates that disintegration is not achieved in the absence of the disintegrant granule.
  • Examples 20 to 22 were prepared by preparing a base powder by granulation as described above for the stock compositions to obtain a composition having the overall compositions given in table 9. Table 9; Ingredient % by weight 20 21 22 Sodium linear alkyl benzene sulphonate 9.01 8.84 8.67 C 13-15 fatty alcohol 7EO, branched.
  • compositions were compacted on a Graseby Laboratory Tablet Press as detailed above for comparative examples C1 and C2 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)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)

Claims (19)

  1. Tablette d'une composition détergente particulaire compactée comprenant un tensioactif de type non-savon et un adjuvant de détergence, dans laquelle la tablette ou une zone distincte de celle-ci comprend :
    a) de 1 à 20 % en poids, sur la base du poids total de la tablette ou de sa zone distincte, de granules d'un délitant comprenant un matériau inorganique insoluble dans l'eau et un agent pouvant gonfler dans l'eau qui, à l'état anhydre, ne représente pas plus de 10 % en poids du poids combiné du matériau inorganique et de l'agent pouvant gonfler dans l'eau, et
    b) des particules solubles dans l'eau favorisant la désintégration contenant au moins 40 %, en poids des particules, d'un ou de plusieurs matériaux choisis dans le groupe constitué par :
    i) les composés ayant une solubilité dans l'eau supérieure à 50 grammes pour 100 grammes d'eau à 20°C, et
    ii) un tripolyphosphate de sodium contenant au moins 50 % de son propre poids de la forme anhydre de phase I, et
    iii) un tripolyphosphate de sodium qui est partiellement hydraté de manière à contenir de l'eau d'hydratation en une quantité qui représente au moins 0,5 % en poids du tripolyphosphate de sodium présent dans les particules.
  2. Tablette selon la revendication 1, dans laquelle les composés ayant une solubilité dans l'eau supérieure à 50 grammes pour 100 grammes d'eau comprennent l'acétate de sodium, le citrate de sodium dihydrate ou l'urée.
  3. Tablette selon la revendication 2, dans laquelle les composés ayant une solubilité dans l'eau supérieure à 50 grammes pour 100 grammes d'eau comprennent l'acétate de sodium trihydraté.
  4. Tablette selon l'une quelconque des revendications 1 à 3, dans laquelle les particules solubles dans l'eau favorisant la désintégration sont présentes en une quantité de 2 à 25 % en poids, sur la base du poids total de la composition.
  5. Tablette selon l'une quelconque des revendications précédentes, dans laquelle au moins une partie des particules solubles dans l'eau favorisant la désintégration est ajoutée à une partie pré-granulée de la composition utilisée pour fabriquer la tablette.
  6. Tablette d'une composition détergente particulaire compactée comprenant un tensioactif de type non-savon et un adjuvant de détergence, dans laquelle la tablette ou une zone distincte de celle-ci comprend :
    a) de 1 à 20 % en poids, sur la base du poids total de la tablette ou de sa zone distincte, de granules d'un délitant comprenant un matériau inorganique insoluble dans l'eau et un agent pouvant gonfler dans l'eau qui, à l'état anhydre, ne représente pas plus de 10 % poids du poids combiné du matériau inorganique et de l'agent pouvant gonfler dans l'eau, et
    b) de 10 à 60 % en poids d'un adjuvant d'aluminosilicate, sur la base du poids total de la tablette ou de sa zone distincte, et une ou plusieurs enzymes de détergence.
  7. Tablette selon la revendication 6, dans laquelle l'adjuvant d'aluminosilicate comprend une zéolite P à maximum d'aluminium ou une zéolite A.
  8. Tablette selon l'une quelconque des revendications précédentes, dans laquelle le matériau inorganique insoluble dans l'eau contenu dans les granules de délitant comprend un aluminosilicate ou une silice.
  9. Tablette selon la revendication 8, dans laquelle l'aluminosilicate comprend une zéolite.
  10. Tablette selon la revendication 9, dans laquelle la zéolithe comprend une zéolithe P.
  11. Tablette selon la revendication 10, dans laquelle la zéolithe comprend une zéolithe P à maximum d'aluminium.
  12. Tablette selon l'une quelconque des revendications précédentes, dans laquelle l'agent pouvant gonfler dans l'eau contenu dans les granules de délitant est choisi dans le groupe constitué par la cellulose, la cellulose réticulée, la carboxyméthylcellulose, la carboxyméthylcellulose sodique, la carboxyméthylcellulose sodique réticulée, l'amidon prégélatinisé, l'amidon réticulé et la polyvinylpyrrolidone réticulée.
  13. Tablette selon la revendication 12, dans laquelle l'agent pouvant gonfler dans l'eau comprend une carboxyméthylcellulose sodique réticulée.
  14. Tablette selon l'une quelconque des revendications précédentes, dans laquelle l'agent pouvant gonfler dans l'eau représente, à l'état anhydre, de 1 à 8 % en poids du poids combiné du matériau inorganique et de l'agent pouvant gonfler dans l'eau contenus dans les granules de délitant.
  15. Tablette selon l'une quelconque des revendications précédentes, dans laquelle le matériau inorganique insoluble dans l'eau contenu dans les granules de délitant comprend une zéolite et les granules de délitant ont une taille moyenne de particules dans la plage de 700 à 1200 micromètres.
  16. Tablette selon l'une quelconque des revendications 1 à 8 ou 12 à 14, dans laquelle le matériau inorganique insoluble dans l'eau contenu dans les granules de délitant comprend une silice et les granules de délitant ont une taille moyenne de particules dans la plage de 250 à 700 micromètres.
  17. Tablette selon l'une quelconque des revendications précédentes, dans laquelle l'agent pouvant gonfler dans l'eau contenu dans les granules de délitant est présent en une quantité inférieure à 2 % en poids, sur la base du poids total de la tablette ou de sa zone distincte.
  18. Tablette selon l'une quelconque des revendications précédentes, dans laquelle l'agent pouvant gonfler dans l'eau a une taille moyenne de particules primaires pas supérieure à 200 µm.
  19. Procédé de fabrication d'une tablette d'une composition particulaire compactée selon les revendications 1 ou 6, ledit procédé comprenant le mélange des granules de délitant soit avec les particules solubles dans l'eau favorisant la désintégration, soit avec le matériau adjuvant d'aluminosilicate et une ou plusieurs enzymes de détergence, et avec d'autres constituants de la composition pour obtenir une composition particulaire, l'introduction d'une certaine quantité de la composition particulaire résultante dans un moule et le compactage de la composition dans le moule pour obtenir la tablette.
EP02716699A 2001-02-05 2002-01-29 Compositions de nettoyage Expired - Lifetime EP1358311B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP02716699A EP1358311B1 (fr) 2001-02-05 2002-01-29 Compositions de nettoyage

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP01200407 2001-02-05
EP01200407 2001-02-05
PCT/EP2002/000945 WO2002062939A1 (fr) 2001-02-05 2002-01-29 Compositions de nettoyage
EP02716699A EP1358311B1 (fr) 2001-02-05 2002-01-29 Compositions de nettoyage

Publications (2)

Publication Number Publication Date
EP1358311A1 EP1358311A1 (fr) 2003-11-05
EP1358311B1 true EP1358311B1 (fr) 2011-08-17

Family

ID=8179853

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02716699A Expired - Lifetime EP1358311B1 (fr) 2001-02-05 2002-01-29 Compositions de nettoyage

Country Status (4)

Country Link
EP (1) EP1358311B1 (fr)
AT (1) ATE520768T1 (fr)
ES (1) ES2368134T3 (fr)
WO (1) WO2002062939A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022268657A1 (fr) 2021-06-24 2022-12-29 Unilever Ip Holdings B.V. Composition de nettoyage monodose

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1418226B1 (fr) * 2002-11-07 2006-10-04 Unilever N.V. Composition détergente
ES2586461B1 (es) * 2015-03-12 2017-12-01 Lorena MARTÍ COMA Composición detergente en forma de pastilla efervescente

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1029263A (en) * 1963-05-17 1966-05-11 Procter & Gamble Ltd Manufacture of detergent briquettes
ZA984570B (en) * 1997-06-06 1999-11-29 Unilever Plc Cleaning compositions.
GB9711829D0 (en) * 1997-06-06 1997-08-06 Unilever Plc Detergent compositions
GB9826097D0 (en) * 1998-11-27 1999-01-20 Unilever Plc Detergent compositions
DE19932569A1 (de) * 1999-07-13 2001-01-18 Henkel Kgaa Wasch- und Reinigungsmittelformkörper, insbesondere für das maschinelle Geschirrspülen

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022268657A1 (fr) 2021-06-24 2022-12-29 Unilever Ip Holdings B.V. Composition de nettoyage monodose
WO2022268728A1 (fr) 2021-06-24 2022-12-29 Unilever Ip Holdings B.V. Composition de nettoyage en doses unitaires

Also Published As

Publication number Publication date
EP1358311A1 (fr) 2003-11-05
ES2368134T3 (es) 2011-11-14
ATE520768T1 (de) 2011-09-15
WO2002062939A1 (fr) 2002-08-15

Similar Documents

Publication Publication Date Title
EP1007621B1 (fr) Compositions detergentes
EP1019484B2 (fr) Compositions de nettoyage
EP0522766B1 (fr) Compositions détergentes sous forme de tablettes
EP0986634B1 (fr) Compositions de nettoyage sous forme de tablette
CA2350467A1 (fr) Compositions detergentes
EP1335968B1 (fr) Compositions de nettoyage
US20030040459A1 (en) Cleaning compositions
EP1232241B1 (fr) Compositions detergentes
EP1358311B1 (fr) Compositions de nettoyage
EP1358312B1 (fr) Compositions de nettoyage
US20020119904A1 (en) Cleaning compositions
EP1398368B1 (fr) Compositions de nettoyage
EP1133548B2 (fr) Compositions detergentes sous forme de comprimes
EP1337618B1 (fr) Comprimes de nettoyage
EP1335967B1 (fr) Compositions de nettoyage
US20020132751A1 (en) Detergent compositions
WO2003014286A1 (fr) Compositions detergentes
EP1389230A1 (fr) Compositions de nettoyage

Legal Events

Date Code Title Description
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

17P Request for examination filed

Effective date: 20030714

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

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

Owner name: UNILEVER N.V.

Owner name: UNILEVER PLC

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

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE 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

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: 60240796

Country of ref document: DE

Effective date: 20111013

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2368134

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20111114

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20110817

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: 20110817

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: 20110817

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: 20110817

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: 20111219

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 520768

Country of ref document: AT

Kind code of ref document: T

Effective date: 20110817

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

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: 20110817

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: 20111118

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: 20110817

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

Ref country code: BE

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: 20110817

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

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: 20110817

26N No opposition filed

Effective date: 20120521

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 NON-PAYMENT OF DUE FEES

Effective date: 20120131

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 60240796

Country of ref document: DE

Effective date: 20120521

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

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

Ref country code: LI

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

Effective date: 20120131

Ref country code: CH

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

Effective date: 20120131

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

Ref country code: IE

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

Effective date: 20120129

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: 20110817

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

Ref country code: DE

Payment date: 20140129

Year of fee payment: 13

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: 20120129

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

Ref country code: IT

Payment date: 20140123

Year of fee payment: 13

Ref country code: FR

Payment date: 20140117

Year of fee payment: 13

Ref country code: ES

Payment date: 20140127

Year of fee payment: 13

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

Ref country code: GB

Payment date: 20140127

Year of fee payment: 13

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 60240796

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20150129

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

Ref country code: GB

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

Effective date: 20150129

Ref country code: DE

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

Effective date: 20150801

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20150930

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

Ref country code: FR

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

Effective date: 20150202

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 NON-PAYMENT OF DUE FEES

Effective date: 20150129

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20160226

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

Ref country code: ES

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

Effective date: 20150130