[go: up one dir, main page]

EP1721962B1 - Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle - Google Patents

Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle Download PDF

Info

Publication number
EP1721962B1
EP1721962B1 EP06075876A EP06075876A EP1721962B1 EP 1721962 B1 EP1721962 B1 EP 1721962B1 EP 06075876 A EP06075876 A EP 06075876A EP 06075876 A EP06075876 A EP 06075876A EP 1721962 B1 EP1721962 B1 EP 1721962B1
Authority
EP
European Patent Office
Prior art keywords
citrate
composition according
dishwashing composition
machine
silicate
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
EP06075876A
Other languages
German (de)
English (en)
Other versions
EP1721962A1 (fr
Inventor
Naresh Dhirajlal Ghatlia
Jean-Paul Janssens
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
Original Assignee
Unilever PLC
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=37074816&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP1721962(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever PLC filed Critical Unilever PLC
Priority to PL06075876T priority Critical patent/PL1721962T3/pl
Priority to EP06075876A priority patent/EP1721962B1/fr
Publication of EP1721962A1 publication Critical patent/EP1721962A1/fr
Application granted granted Critical
Publication of EP1721962B1 publication Critical patent/EP1721962B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/046—Salts
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0073—Anticorrosion compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2086—Hydroxy carboxylic acids-salts thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/26—Organic compounds containing nitrogen
    • C11D3/33—Amino carboxylic acids

Definitions

  • the present invention is in the field of machine dishwashing. More specifically, the invention encompasses automatic dishwashing detergents and their use in a dish washing process.
  • a consumer would use three products to wash dishes in an automatic dishwashing machine.
  • Salt would be added to the salt compartment to soften water.
  • a dishwashing detergent composition would serve to clean the articles, and a rinse aid would be used in the final steps of the dishwashing process to avoid streaks and smears on the articles.
  • "4 in 1" products comprise, in addition to the ingredients of the "3 in 1" products, a glass protection agent.
  • a builder generally serves to improve and extend the action of surfactant.
  • a builder may provide this contribution in a number of ways, e.g. by binding of calcium and magnesium ions, binding of transition metal ions, peptisation and suspension of soil in solution, provision of alkalinity and structuring/solubilising powder. The binding of calcium and magnesium is the most relevant function among these.
  • Suitable replacers include carbonate, citrate, zeolite, silicate and amino polycarboxylic compounds such as methylglycine diacetic acid (MGDA) and variants thereof e.g. NTA (nitrile triacetic acid), GDA (glutamic diacetic acid), DPA (dipicolinic acid) and IDS (imino disuccinic acid).
  • MGDA methylglycine diacetic acid
  • NTA nitrile triacetic acid
  • GDA glutmic diacetic acid
  • DPA dipicolinic acid
  • IDS amino disuccinic acid
  • citrate The most common replacer of phosphate builder is citrate.
  • a drawback of the inclusion of citrate is that its functionality is not optimal in a hard water environment. Natural water contains calcium and magnesium ions which can act as counterion to carbonate. Under certain conditions this may lead to the precipitation of calcium/magnesium carbonate. This precipitate is white on glass and washware and is certainly not desired by consumers. The level of these cations is referred to as the total hardness of water which is expressed as milligrams of equivalent calcium carbonate (Mw 100) per liter (ppm).Reference is made to L.S. Clesceri et al, Standard methods for the examination of water and wastewater, 17th edition, American Public Health Association, Washington DC, 1989 . The hardness of natural waters can range from only a few ppm up to over 400 ppm in some areas.
  • the invention relates to a multifunctional dishwashing composition for use in an automatic dish washer, said composition containing less than 1% phosphates, wherein the composition comprises
  • the invention further relates to a method for washing articles in a mechanical dishwashing machine comprising treating the articles with a wash liquor comprising the composition according to the invention.
  • the invention relates to the use of a composition according to the invention in an automatic dishwashing machine so no salt is required for rejuvenation of ion exchange material within the machine.
  • citrate or aminocarboxylic compound or another acid this is intended to encompass the acid, a salt thereof or a combination.
  • compositions according to the invention comprise a builder.
  • the compositions are essentially free of phosphate and therefore another builder is included.
  • essentially free of phosphate is defined as containing less than 1 wt% phosphate-compound on total weight of the composition.
  • phosphate containing compounds are tripolyphosphates, polyphosphates, hexametaphosphate, orthophosphate, and the alkalimetal (preferably sodium) salts thereof.
  • the builder functionality in these compositions is found in the combination of the amino polycarboxylic compound and citrate.
  • the amount of citrate is from 30 to 70 wt% on the total weight of citrate and amino polycarboxylic compound.
  • the amount of citrate is from 40 to 60 wt% on the total weight of citrate and amino polycarboxylic compound.
  • the total level of citrate in the compositions is preferably from 10 to 30 wt%, more preferred from 10 to 25 wt%.
  • the total level of amino polycarboxylic compound is preferably from 10 to 40 wt%, more preferred from 20 to 30 wt% on total weight of the composition.
  • Citrate is preferably present in the form of its sodium salt.
  • the amino polycarboxylic compound is selected fom MGDA and IDS.
  • the most preferred type of amino polycarboxylic compound is MGDA.
  • the composition comprises a further builder which may be selected for example from the group comprising alkali metal carbonates, bicarbonates, borates and zeolites.
  • the composition comprises from 0 to 5 wt% of silicate.
  • silicate is present in amounts up to 30 wt% or even higher, around 50 wt%. Purpose of the silicate in those known compositions is often to prevent fading of colours on glaze porcelain and decorated glasses via corrosion, as well as on enamel and metal corrosion.
  • the amount of silicate present in the composition of the current invention should be far less than 30 wt%, most preferably even as low as possible, while use of the machine dishwash detergent composition of the invention does not lead to negative effects from the reduction or even omission of silicate compounds in said composition.
  • the machine dishwash detergent composition of the invention does not lead to negative effects from the reduction or even omission of silicate compounds in said composition.
  • silicium compounds in the form of silicate there is a maximum amount of silicium compounds in the form of silicate to be present.
  • the total amount of silicate present is 5 wt%. If any silicate is present in the composition or the process of the current invention, it is preferred that the silicate is chosen from the group of alkali metal silicates.
  • the silicate may provide pH adjusting capability and protection against corrosion of metals and against attack on décor on dishware, including fine china and glassware benefits.
  • the alkali metal silicate is hydrous, having from 15% to 25% water, more preferably, from 17% to 20%.
  • the silicate levels indicated in the specification are calculated as SiO 2 .
  • the highly alkali metasilicates can in principle be employed, but in general, yield too high a pH to be suitable for application in the compositions of the current invention. Therefore, the less alkaline hydrous alkali metal silicates having a SiO 2 :M 2 O ratio of from 2.0 to 2.4 are, greatly preferred. Anhydrous forms of the alkali metal silicates with a SiO 2 :M 2 O ratio of 2.0 or more are less preferred because they tend to be significantly less soluble than the hydrous alkali metal silicates having the ratio of less than 2.
  • alkali metal silicates sodium and potassium, and especially sodium, silicates are preferred.
  • a particularly preferred alkali metal silicate is a granular hydrous sodium silicate having a SiO 2 :Na 2 O ratio of from 2.0 to 2.4 available from PQ Corporation, named Britesil H20 and Britesil H24. Most preferred is a granular hydrous sodium silicate having a SiO 2 :Na 2 O ratio of 2.0, in particular for application in machine dishwash detergent compositions applied in powder or tablet form. While typical forms, i.e.
  • silicate particles powder and granular, of hydrous silicate particles are suitable, preferred silicate particles having a mean particle size between 300 and 900 ⁇ m and less than 40% smaller than 150 ⁇ m and less than 5% larger than 1700 ⁇ m. Particularly preferred is a silicate particle with a mean particle size between 400 and 700 ⁇ m with less than 20% smaller than 150 ⁇ m and less than 1% larger then 1700 ⁇ m.
  • Machine dishwash compositions according to the invention comprise less than 5 wt.% of silicate.
  • a maximum amount of 4 wt.% silicate further preferred an amount of less than 3 wt.%, more preferred of less than 2 wt.% is present.
  • Even better visible glass corrosion inhibition results are observed at slicate levels of less than 1.5 wt.%, more desirably less than 0.8 wt.%. Therefore, it is preferred that the level of silicate in the dishwash composition, more particularly, in the water of the wash cycle, is as low as possible. Accordingly, in a specific embodiment of the invention, the machine dishwash detergent composition is substantially free of silicate.
  • composition of the invention comprises a water soluble salt of bismuth.
  • levels indicated are calculated as bismuth ions, unless indicated otherwise.
  • a soluble salt of bismuth is meant, unless indicated otherwise.
  • the level of water soluble bismuth salt in the machine dishwash detergent composition of the invention is less than or equal to 3 wt.%, based on the total composition.
  • the composition of the invention contains at least 0.05 wt.%.
  • the composition of the invention comprises from 0.1 to 2 wt% of the water soluble salt of bismuth. Said concentration ranges are based on the average and recommended amount of detergent composition used per main wash cycle.
  • Machine dishwash detergent compositions according to the invention may suitably be dosed in the wash liquor at levels of from 2 g/l to 10 g/l.
  • Water soluble Bi-salts suitable for use in the detergent compositions of the invention are in particular selected from the group of bismuth acetate, acetate dihydrate, bromide, butyrate, citrate, citrate dihydrate, chloride, iodide, iodide dihydrate, caproate, formate, formate dihydrate, fumarate, gluconate, glycinate, lactate, malate, maleate, nitrate, nitrate trihydrate, nitrate hexahydrate, phenolsulphonate, sulfate monohydrate, sulfate heptahydrate, sulfate hexahydrate, salicylate, succinate, tartrate, valerate, saccharinate, and carboxymethyl oxysuccinate. It is preferred to use a water soluble bismuth salt composition chosen from the group of acetate, formate, and sulfate. Mixtures of any of the salts mentioned can also be used.
  • composition of the current invention in any embodiment thereof, is substantially free of, and further preferred, does not comprise any aluminum or aluminum compound.
  • Aluminum ions are multivalent, and presence thereof in the composition will result in precipitation of insoluble salts thereof. This is disadvantageous as it will result in deposits on the glasware.
  • suitable surfactant systems for use in the machine dishwash detergent compositions of the current invention comprise ethoxylated and/or propoxylated nonionic surfactants, more preferably selected from nonionic ethoxylated / propoxylated fatty alcohol surfactants having a cloud point in water of 14 °C or less, preferably of 10 °C or less when used in the so called multifunctional systems.
  • the indicated restriction is less critical. In general, preferably less than 5 wt.% of a surfactant is present.
  • Surfactants, within the invention are components within the classification as described in " Surfactant Science Series", Vol.82, Handbook of detergents, part A: Properties, chapter 2 (Surfactants, classification), G. Broze (ed .).
  • nonionic surfactants for use in the invention are found in the low- to non-foaming ethoxylated/propoxylated straight-chain alcohols of the Plurafac® LF series, supplied by the BASF Company and the Synperonic NCA series supplied by ICI/ Uniqema. Also of interest are the endcapped ethoxylated alcohols available as the SLF 18 series from BASF/Olin.
  • the ethoxylated and/or propoxylated nonionic surfactants are present at levels of at least 0.5 wt.%, more preferably 1 to 5 wt.% of the total composition.
  • the total amount thereof present should be at levels of less than 5 wt.%, and preferably at levels of 2 wt.% or below. Furthermore, if any anionic surfactant is present, it is preferred that an antifoam agent to suppress foaming is present.
  • Enzymes may be present in the compositions of the invention.
  • Examples of enzymes suitable for use in the cleaning compositions of this invention include lipases, peptidases, amylases (amylolytic enzymes) and others which degrade, alter or facilitate the degradation or alteration of biochemical soils and stains encountered in cleansing situations so as to remove more easily the soil or stain from the object being washed to make the soil or stain more removable in a subsequent cleansing step. Both degradation and alteration can improve soil removal.
  • enzymes are lipases, amylases and proteases.
  • the enzymes most commonly used in machine dishwashing compositions are amylolytic enzymes.
  • the composition of the invention also contains a proteolytic enzyme. Enzymes may be present in a weight percentage amount of from 0.2 to 7% by weight.
  • Bleach material is preferably incorporated in the composition.
  • bleaching agents both the peroxygen bleaching agents and the chlorine-releasing agents are suitable for inclusion in the machine dishwashing compositions.
  • 1-5 wt.% of a chlorine bleaching agent may be used.
  • the bleach material can completely or partially, be encapsulated.
  • the bleach material may be a chlorine- or bromine-releasing agent or a peroxygen compound. Peroxygen based bleach materials are however preferred.
  • Inorganic peroxygen-generating compounds are also typically used as the bleaching material of the present invention.
  • these materials are acids and corresponding salts of monopersulphate, perborate monohydrate, perborate tetrahydrate, and percarbonate.
  • Monoperoxy acids useful herein include alkyl peroxy acids and aryl peroxyacids such as peroxybenzoic acid and ring-substituted peroxybenzoic acids (e.g. peroxy-alpha-naphthoic acid), aliphatic and substituted aliphatic monoperoxy acids (e.g. peroxylauric acid and peroxystearic acid), and phthaloyl amido peroxy caproic acid (PAP).
  • alkyl peroxy acids and aryl peroxyacids such as peroxybenzoic acid and ring-substituted peroxybenzoic acids (e.g. peroxy-alpha-naphthoic acid), aliphatic and substituted aliphatic monoperoxy acids (e.g. peroxylauric acid and peroxystearic acid), and phthaloyl amido peroxy caproic acid (PAP).
  • peroxybenzoic acid and ring-substituted peroxybenzoic acids
  • diperoxy acids useful herein include alkyl diperoxy acids and aryldiperoxy acids, such as 1,12-di-peroxydodecanedioic acid (DPDA), 1,9-diperoxyazelaic acid, diperoxybrassylic acid, diperoxysebacic acid and diperoxyisophthalic acid, and 2-decyldiperoxybutane-1,4-dioic acid.
  • DPDA 1,12-di-peroxydodecanedioic acid
  • 1,9-diperoxyazelaic acid diperoxybrassylic acid
  • diperoxysebacic acid and diperoxyisophthalic acid diperoxyisophthalic acid
  • 2-decyldiperoxybutane-1,4-dioic acid 2-decyldiperoxybutane-1,4-dioic acid.
  • Peroxyacid bleach precursors are well known in the art. As non-limiting examples can be named N,N,N',N'-tetraacetyl ethylene diamine (TAED), sodium nonanoyloxybenzene sulphonate (SNOBS), sodium benzoyloxybenzene sulphonate (SBOBS) and the cationic peroxyacid precursor (SPCC) as described in US-A-4,751,015 .
  • TAED N,N,N',N'-tetraacetyl ethylene diamine
  • SNOBS sodium nonanoyloxybenzene sulphonate
  • SBOBS sodium benzoyloxybenzene sulphonate
  • SPCC cationic peroxyacid precursor
  • a bleach catalyst such as the manganese complex, e.g. Mn-Me TACN, as described in EP-A-0458397 , or the sulphonimines of US-A-5,041,232 and US-A-5,047,163 , this may be presented in the form of a second encapsulate separately from the bleach capsule or granule.
  • Cobalt catalysts can also be used.
  • peroxygen bleaching agents a suitable range is also from 0.5% to 3% avO (available Oxygen).
  • the amount of bleach material in the wash liquor is at least 0.00125 wt.% and at most 0.03 wt.% avO by weight of the liquor.
  • Anti-tarnishing agents such as benzatriazole and those described in EP 723 577 (Unilever) may also be included.
  • Optional ingredients are, for example, buffering agents, reducing agents, e.g., borates, alkali metal hydroxide and the well-known enzyme stabilisers such as the polyalcohols, e.g. glycerol and borax, crystal-growth inhibitors, threshold agents, perfumes and dyestuffs and the like.
  • binding agents can be used e.g. modified starches.
  • Reducing agents may be used, e.g., to prevent the appearance of an enzyme-deactivating concentration of oxidant bleach compound. Suitable agents include reducing sulphur-oxy acids and salts thereof.
  • alkali metal and ammonium salts of sulphuroxy acids including ammonium sulphite ((NH 4 ) 2 SO 3 ), sodium sulphite (Na 2 SO 3 ), sodium bisulphite (NaHSO 3 ), sodium metabisulphite (Na 2 S 2 O 3 ), potassium metabisulphite (K 2 S 2 O 5 ), lithium hydrosulphite (Li 2 S 2 O 4 ), etc., sodium sulphite being particularly preferred.
  • ammonium sulphite (NH 4 ) 2 SO 3 ), sodium sulphite (Na 2 SO 3 ), sodium bisulphite (NaHSO 3 ), sodium metabisulphite (Na 2 S 2 O 3 ), potassium metabisulphite (K 2 S 2 O 5 ), lithium hydrosulphite (Li 2 S 2 O 4 ), etc.
  • Another useful reducing agent though not particularly preferred for reasons of cost, is ascorbic acid.
  • the amount of reducing agents to be used may vary from case to case depending on the type of bleach and the form it is in, but normally a range of about 0.01 wt.% to about 1.0 wt.%, preferably from about 0.02 wt.% to about 0.5 wt.%, will be sufficient.
  • the machine dishwash detergent composition furthermore comprises at least one dispersing polymer.
  • Such polymers have been found to have a beneficial effect on the efficiency of the water soluble zinc salt, in particular, it has been found that such polymers reduce the precipitation of any insoluble zinc salt.
  • Dispersing polymers as referred to in this invention are chosen from the group of anti-spotting agents and/or anti-scaling agents.
  • anti-spotting polymeric agents examples include Acusol 460 ND (ex Rohm & Haas), whereas also synthetic clays, and preferably those synthetic clays which have a high surface area are very useful to prevent spots, in particular those formed where soil and dispersed remnants are present at places where the water collects on the glass and spots formed when the water subsequently evaporates.
  • Antispotting systems such as Acusol 460 ND are advantageous in the so called multifunctional systems.
  • suitable anti-scaling agents include organic phosphonates, amino carboxylates, polyfunctionally-substituted compounds, and mixtures thereof.
  • Particularly preferred anti-scaling agents are organic phosphonates such as ⁇ -hydroxy-2 phenyl ethyl diphosphonate, ethylene diphosphonate, hydroxy 1,1-hexylidene, vinylidene 1,1-diphosphonate, 1,2-dihydroxyethane 1,1-diphosphonate and hydroxy-ethylene 1,1-diphosphonate.
  • EDHP hydroxy-ethylene 1,1-diphosphonate
  • 2-phosphono-butane 1,2,4-tricarboxylic acid
  • water soluble dispersing polymers prepared from an allyloxybenzenesulfonic acid monomer, a methallyl sulfonic acid monomer, a copolymerizable nonionic monomer and a copolymerizable olefinically unsaturated carboxylic acid monomer as described in US 5 547 612 or known as acrylic sulphonated polymers as described in EP 851 022 .
  • Polymers of this type include polyacrylate with methyl methacrylate, sodium methallyl sulphonate and sulphophenol methallyl ether such as Alcosperse 240 supplied by Alco.
  • terpolymer containing polyacrylate with 2-acrylamido-2 methylpropane sulphonic acid such as Acumer 3100 supplied by Rohm and Haas.
  • polymers and co-polymers of acrylic acid having a molecular weight between 500 and 20,000 can also be used, such as homo-polymeric polycarboxylic acid compounds with acrylic acid as the monomeric unit.
  • the average weight of such homo-polymers in the acid form preferably ranges from 1,000 to 100,000 particularly from 3,000 to 10,000 e.g. SokolanTM PA 25 from BASF.
  • polycarboxylates co-polymers derived from monomers of acrylic acid and maleic acid The average molecular weight of these polymers in the acid form preferably ranges from 4,000 to 70,000.
  • anti-scaling agents may be used, particularly useful is a mixture of organic phosphonates and polymers of acrylic acid with methyl methacrylate, sodium methallyl sulfonate.
  • the level of anti-scaling agent is from 0.2 to 10 wt.% of the total composition, preferably from 0.5 to 5 wt.%, and further preferred 0.5 to 4 wt.%.
  • Suitable forms for the machine dishwash detergent composition are a powder, tablet, gel or liquid detergent composition, and mixtures thereof.
  • the compositions are unit dose compositions such as tablets or gel particles. Most preferred the compositions are in the form of tablets. Unit dose compositions such as tablets or gels may be wrapped in a water soluble wrap for easy handling.
  • the composition according to the invention comprises a rinse aid composition/ingredient.
  • Rinse aid ingredients are ingredients that effect that final appearance of the table ware that is washed. Examples of such ingredients are commercially available under the tradenames SLF, Acusol and Alcosperse.
  • the invention relates to a method for washing articles in a mechanical dishwash machine comprising the steps of treating the articles with a wash liquor comprising a dishwashing composition according to the invention as specified above, wherein no rejuvenation of ion exchange material within the machine is needed.
  • compositions especially suitable for this use are multifunctional compositions. Most preferably, the consumer no longer needs to add salt for rejuvenation of the ion exchange material because this functionality is already built into the composition.
  • the invention relates to the use of a dishwashing composition according to the invention for use in an automatic dishwashing machine so no salt is required for the rejuvenation of ion exchange material within the machine.

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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Claims (8)

  1. Composition multifonctionnelle pour Lave-vaisselle à utiliser dans un lave-vaisselle automatique, ladite composition contenant moins de 1 % en poids de phosphates, dans laquelle la composition contient :
    a) un tensio-actif dans une quantité d'au plus 10 % en poids ;
    b) un composé amino-polycarboxylique choisi parmi l'acide méthylglycine-diacétique (MGDA) et l'acide iminodiacétique (UDS), dans une quantité comprise entre 5 et 70 % en poids,
    c) du citrate dans une quantité de 5 à 40 % en poids ;
    d) de 0,05 à 3 % en poids de sel de bismuth soluble dans l'eau ; et
    e) de 0 à 5 % en poids de silicate,
    dans laquelle la quantité de citrate est comprise entre 30 et 70 % en poids, sur la base du poids total du citrate et du composé amino-polycarboxylique.
  2. Composition pour lave-vaisselle selon la revendication 1, dans laquelle le composé amino-polycarboxylique comprend du MGDA.
  3. Composition pour lave-vaisselle selon la revendication 1 ou 2, dans laquelle la composition comprend un ingrédient d'aide au rinçage.
  4. Composition pour lave-vaisselle selon l'une quelconque des revendications 1 à 3, qui contient moins de 0,8 % en poids de silicate.
  5. Composition pour lave-vaisselle selon l'une quelconque des revendications 1 à 4, dans laquelle la quantité de citrate est comprise entre 40 et 60 % en poids, sur la base du poids total de citrate et de composé amino-polycarboxylique.
  6. Composition pour lave-vaisselle selon l'une quelconque des revendications 1 à 5, qui comprend un polymère anti-tartre.
  7. Procédé de lavage d'articles dans un lave-vaisselle mécanique, comprenant le traitement d'articles avec un détergent comprenant une composition pour lave-vaisselle selon l'une quelconque des revendications 1 à 6, dans lequel aucun rajeunissement de matériau à échange d'ion dans la machine n'est nécessaire.
  8. Utilisation d'une composition pour lave-vaisselle selon l'une quelconque des revendications 1 à 6, dans un lave-vaisselle automatique, de sorte qu'aucun sel n'est requis pour le rajeunissement du matériau à échange d'ions dans la machine.
EP06075876A 2005-05-11 2006-04-13 Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle Active EP1721962B1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
PL06075876T PL1721962T3 (pl) 2005-05-11 2006-04-13 Kompozycja do mycia naczyń oraz sposób zmywania naczyń
EP06075876A EP1721962B1 (fr) 2005-05-11 2006-04-13 Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP05076102 2005-05-11
EP06075876A EP1721962B1 (fr) 2005-05-11 2006-04-13 Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle

Publications (2)

Publication Number Publication Date
EP1721962A1 EP1721962A1 (fr) 2006-11-15
EP1721962B1 true EP1721962B1 (fr) 2008-08-13

Family

ID=37074816

Family Applications (1)

Application Number Title Priority Date Filing Date
EP06075876A Active EP1721962B1 (fr) 2005-05-11 2006-04-13 Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle

Country Status (2)

Country Link
EP (1) EP1721962B1 (fr)
PL (1) PL1721962T3 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8722606B2 (en) 2010-03-09 2014-05-13 Rohm And Haas Company Scale-reducing additive for automatic dishwashing systems
WO2024089079A1 (fr) 2022-10-25 2024-05-02 Symrise Ag Composition de nettoyage de vaisselle et/ou de rinçage de vaisselle présentant des propriétés de finition améliorées

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0522658D0 (en) 2005-11-07 2005-12-14 Reckitt Benckiser Nv Composition
GB0611206D0 (en) 2006-06-07 2006-07-19 Reckitt Benckiser Nv Detergent composition
CA2666457A1 (fr) * 2006-10-16 2008-04-24 Danisco Us Inc., Genencor Division Detergents de vaisselle sans phosphate
GB0625586D0 (en) * 2006-12-21 2007-01-31 Reckitt Benckiser Nv Composition
DE102007003885A1 (de) * 2007-01-19 2008-07-24 Lanxess Deutschland Gmbh Geschirrreinigungsmittel
DE102007006627A1 (de) * 2007-02-06 2008-08-07 Henkel Ag & Co. Kgaa Reinigungsmittel
DE102007006630A1 (de) 2007-02-06 2008-08-07 Henkel Ag & Co. Kgaa Reinigungsmittel
DE102007006628A1 (de) 2007-02-06 2008-08-07 Henkel Ag & Co. Kgaa Reinigungsmittel
DE102007006629A1 (de) 2007-02-06 2008-08-07 Henkel Ag & Co. Kgaa Reinigungsmittel
WO2008095554A2 (fr) * 2007-02-06 2008-08-14 Henkel Ag & Co. Kgaa Détergents
GB0718944D0 (en) * 2007-09-28 2007-11-07 Reckitt Benckiser Nv Detergent composition
DE102007059968A1 (de) * 2007-12-11 2009-06-18 Henkel Ag & Co. Kgaa Reinigungsmittel
EA201001199A1 (ru) * 2008-01-24 2011-02-28 Юнилевер Н.В. Композиции детергентов для посудомоечных машин
EP3061744B1 (fr) * 2008-04-01 2018-05-09 Unilever N.V. Préparation de granulés à écoulement libre d'acide diacétique methylglycine
PL2380961T3 (pl) 2010-04-23 2018-10-31 The Procter & Gamble Company Kompozycja detergentu
EP2383329A1 (fr) * 2010-04-23 2011-11-02 The Procter & Gamble Company Particule
ES2579217T3 (es) 2010-04-23 2016-08-08 The Procter & Gamble Company Partícula
RU2607085C2 (ru) * 2011-10-19 2017-01-10 Басф Се Составы, их применение в качестве или для приготовления средств для мытья посуды и получение составов
CA2849358A1 (fr) 2011-10-19 2013-04-25 Basf Se Formulations, leur utilisation comme detergents pour vaisselle ou pour la fabrication de detergents pour vaisselle, et leur preparation
RU2623443C2 (ru) 2011-10-19 2017-06-26 Басф Се Составы, их применение в качестве или для приготовления средств для мытья посуды и получение составов
DE102011084934A1 (de) * 2011-10-21 2013-04-25 Henkel Ag & Co. Kgaa Klarspül- und Geschirrspülmittel
GB201214558D0 (en) * 2012-08-15 2012-09-26 Reckitt Benckiser Nv Detergent granule
RU2656214C2 (ru) * 2013-04-02 2018-06-01 Басф Се Композиции, их применение в качестве или для получения средств для мытья посуды и их получение
CN105992813B (zh) 2014-02-20 2019-01-29 荷兰联合利华有限公司 机洗餐具组合物
US20170275567A1 (en) * 2014-09-19 2017-09-28 Basf Se Detergent composition
EP3050955B2 (fr) * 2015-02-02 2023-11-08 The Procter & Gamble Company Emballage de détergent
EP3050948B1 (fr) 2015-02-02 2018-09-19 The Procter and Gamble Company Nouvelle utilisation d'un agent complexant
ES2714130T3 (es) * 2015-02-02 2019-05-27 Procter & Gamble Composición detergente
EP3275988B1 (fr) 2016-07-26 2020-07-08 The Procter and Gamble Company Composition de détergent de lave-vaisselle automatique
EP3275986B1 (fr) 2016-07-26 2020-07-08 The Procter and Gamble Company Composition de détergent de lave-vaisselle automatique
DE102017212561A1 (de) 2017-07-21 2019-01-24 Henkel Ag & Co. Kgaa Geschirrspülmittel enthaltend Citratdihydrat und -anhydrat
CN108865471B (zh) * 2018-08-09 2020-09-25 广州立白企业集团有限公司 一种具有防蚀效果的自动洗碗机专用洗涤剂组合物
EP3623456A1 (fr) 2018-09-12 2020-03-18 CLARO Products GmbH Moyen de protection d'argent
CN115210349A (zh) 2020-02-28 2022-10-18 联合利华知识产权控股有限公司 餐具洗涤剂产品
TW202313944A (zh) * 2021-07-23 2023-04-01 美商阿散德性能材料營運公司 含有氨基羧酸螯合劑的水溶液

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1586067A (en) * 1976-10-28 1981-03-18 Procter & Gamble Detergent composition
US6165970A (en) * 1996-03-29 2000-12-26 The Procter & Gamble Company Detergent composition comprising acrylic acid-based polymer and amino tricarboxylic acid-based compound
EP1113070B1 (fr) * 1996-06-21 2008-03-19 Reckitt Benckiser N.V. Composition de lavage automatique de la vaisselle à basse alkalinité contenant du MGDA

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8722606B2 (en) 2010-03-09 2014-05-13 Rohm And Haas Company Scale-reducing additive for automatic dishwashing systems
WO2024089079A1 (fr) 2022-10-25 2024-05-02 Symrise Ag Composition de nettoyage de vaisselle et/ou de rinçage de vaisselle présentant des propriétés de finition améliorées

Also Published As

Publication number Publication date
PL1721962T3 (pl) 2009-01-30
EP1721962A1 (fr) 2006-11-15

Similar Documents

Publication Publication Date Title
EP1721962B1 (fr) Compositions detergentes pour lave vaisselle et procédé pour nettoyer la vaiselle
EP2245129B1 (fr) Compositions de détergent pour machine à laver la vaisselle
US5900395A (en) Machine dishwashing tablets containing an oxygen bleach system
CA2542750C (fr) Methodes cycliques completes de protection de la verrerie contre l'irisation dans les lave-vaisselle automatiques, faisant appel a des matieres contenant du zinc
EP0770121B1 (fr) Procede et composition de lavage
EA026023B1 (ru) Композиция моющего средства, содержащая глутамин-n,n-диацетат, воду и отбеливатель
EP2997121B1 (fr) Composition détergente pour lave-vaisselle
US20090082245A1 (en) Method for formulating a branded cleaning product
US20090099054A1 (en) Method for formulating a reduced phosphorus branded cleaning product or cleaning system
EP4347767B1 (fr) Détergent de lave-vaisselle
WO2025011917A1 (fr) Composition détergente pour lave-vaisselle
EP1328613B1 (fr) Compositions pour laver la vaisselle
WO2010061239A1 (fr) Procédé de formulation d'un produit de nettoyage de marque
US6310023B1 (en) Machine dish wash compositions
EP1328611B1 (fr) Compositions pour lave-vaisselle
WO2023030882A1 (fr) Détergent pour lave-vaisselle
EP4347766B1 (fr) Détergent de lave-vaisselle
CA2044954A1 (fr) Composition et methode anti-incrustation pour tissus
EP4284904A1 (fr) Liquide détergent pour lave-vaisselle professionnel
ZA200105695B (en) Dish washing process and compolsitions relating thereto.
WO2010061240A1 (fr) Procédé de formulation d’un produit de nettoyage ou un système de nettoyage de marque à teneur réduite en phosphore
WO2001002524A1 (fr) Composition pour lave-vaisselle
EP1287107A1 (fr) Compositions pour vaisselle

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: 20060907

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK YU

17Q First examination report despatched

Effective date: 20070222

RIN1 Information on inventor provided before grant (corrected)

Inventor name: JANSSENS, JEAN-PAUL

Inventor name: GHATLIA, NARESH DHIRAJLAL

AKX Designation fees paid

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR

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 BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK 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: CH

Ref legal event code: NV

Representative=s name: E. BLUM & CO. AG PATENT- UND MARKENANWAELTE VSP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 602006002167

Country of ref document: DE

Date of ref document: 20080925

Kind code of ref document: P

REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 20081007

REG Reference to a national code

Ref country code: SE

Ref legal event code: TRGR

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: 20080813

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: 20081213

REG Reference to a national code

Ref country code: PL

Ref legal event code: T3

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

Ref country code: SI

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

Effective date: 20080813

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: 20080813

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: 20081124

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: 20080813

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: 20080813

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: 20081113

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

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: 20080813

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: 20080813

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: 20080813

26 Opposition filed

Opponent name: RECKITT BENCKISER (UK) LIMITED

Effective date: 20090512

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: 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: 20080813

NLR1 Nl: opposition has been filed with the epo

Opponent name: RECKITT BENCKISER (UK) LIMITED

PLAF Information modified related to communication of a notice of opposition and request to file observations + time limit

Free format text: ORIGINAL CODE: EPIDOSCOBS2

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: 20090430

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

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: 20081114

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

Ref country code: HU

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: 20090214

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: 20080813

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

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

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 20120625

REG Reference to a national code

Ref country code: DE

Ref legal event code: R100

Ref document number: 602006002167

Country of ref document: DE

Effective date: 20120625

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 11

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 12

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 13

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

Ref country code: LU

Payment date: 20200420

Year of fee payment: 15

Ref country code: IE

Payment date: 20200420

Year of fee payment: 15

Ref country code: FI

Payment date: 20200421

Year of fee payment: 15

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

Ref country code: SE

Payment date: 20200427

Year of fee payment: 15

REG Reference to a national code

Ref country code: NL

Ref legal event code: PD

Owner name: UNILEVER IP HOLDINGS B.V.; NL

Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), ASSIGNMENT; FORMER OWNER NAME: UNILEVER N.V.

Effective date: 20210413

REG Reference to a national code

Ref country code: BE

Ref legal event code: PD

Owner name: UNILEVER IP HOLDINGS B.V.; NL

Free format text: DETAILS ASSIGNMENT: CHANGE OF OWNER(S), ASSIGNMENT; FORMER OWNER NAME: UNILEVER N.V.

Effective date: 20210607

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602006002167

Country of ref document: DE

Owner name: UNILEVER GLOBAL IP LIMITED, WIRRAL, GB

Free format text: FORMER OWNER: UNILEVER N.V., ROTTERDAM, NL

REG Reference to a national code

Ref country code: FI

Ref legal event code: MAE

REG Reference to a national code

Ref country code: SE

Ref legal event code: EUG

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: 20210413

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

Ref country code: FI

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

Effective date: 20210413

Ref country code: SE

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

Effective date: 20210414

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20220203 AND 20220209

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: 20210413

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

Ref country code: PT

Payment date: 20220331

Year of fee payment: 17

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

Ref country code: IT

Payment date: 20220421

Year of fee payment: 17

Ref country code: GB

Payment date: 20220420

Year of fee payment: 17

Ref country code: DE

Payment date: 20220420

Year of fee payment: 17

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

Ref country code: TR

Payment date: 20220411

Year of fee payment: 17

Ref country code: CH

Payment date: 20220421

Year of fee payment: 17

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

Ref country code: NL

Payment date: 20230419

Year of fee payment: 18

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

Ref country code: FR

Payment date: 20230420

Year of fee payment: 18

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

Ref country code: PL

Payment date: 20230403

Year of fee payment: 18

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

Ref country code: BE

Payment date: 20230419

Year of fee payment: 18

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602006002167

Country of ref document: DE

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Effective date: 20230413

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: 20230413

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

Ref country code: PT

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

Effective date: 20231013

Ref country code: LI

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

Effective date: 20230430

Ref country code: GB

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

Effective date: 20230413

Ref country code: DE

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

Effective date: 20231103

Ref country code: CH

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

Effective date: 20230430

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: 20230413

REG Reference to a national code

Ref country code: NL

Ref legal event code: MM

Effective date: 20240501

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20240430

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

Ref country code: NL

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

Effective date: 20240501

Ref country code: BE

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

Effective date: 20240430

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: 20240430

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

Ref country code: NL

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

Effective date: 20240501

Ref country code: FR

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

Effective date: 20240430

Ref country code: BE

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

Effective date: 20240430

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

Ref country code: PL

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

Effective date: 20240413