EP1328611A1 - Dish-washing compositions - Google Patents

Dish-washing compositions

Info

Publication number
EP1328611A1
EP1328611A1 EP01982443A EP01982443A EP1328611A1 EP 1328611 A1 EP1328611 A1 EP 1328611A1 EP 01982443 A EP01982443 A EP 01982443A EP 01982443 A EP01982443 A EP 01982443A EP 1328611 A1 EP1328611 A1 EP 1328611A1
Authority
EP
European Patent Office
Prior art keywords
composition
machine
nonionic surfactant
water
less
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.)
Granted
Application number
EP01982443A
Other languages
German (de)
French (fr)
Other versions
EP1328611B1 (en
Inventor
Marco Franciscus Van Dijk
Alan Digby Tomlinson
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 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 EP01982443A priority Critical patent/EP1328611B1/en
Publication of EP1328611A1 publication Critical patent/EP1328611A1/en
Application granted granted Critical
Publication of EP1328611B1 publication Critical patent/EP1328611B1/en
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
    • 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
    • C11D17/0091Dishwashing 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • the present invention is in the field of machine dishwashing. More specifically, the invention encompasses compositions for use in a machine dish wash formulation, which do not necessitate the addition of salt or rinse aid to the machine .
  • To wash articles in a commercially available dish washing machine usually entails using three product types. Salt is added to the salt compartment to soften the water, a dishwashing formulation is used to clean the articles, and a rinse aid is used to ensure that the articles are rinsed with no streaks or smears .
  • WO 00/06684 discloses a machine dish wash tablet.
  • the tablet has a base composition that carries out it's function in the main wash cycle, and a separate core that acts as a rinse aid in the rinse cycle of the machine.
  • a separate core that acts as a rinse aid in the rinse cycle of the machine.
  • Such a tablet is complicated to manufacture.
  • WO 95/07330 Procter & Gamble
  • US 5358655 Hexkel
  • the present invention relates to a composition for washing dishes that obviates the need for salt and rinse aid in the machine dishwashing process .
  • the present invention relates to a machine dish wash composition
  • a machine dish wash composition comprising at least 4.0 wt% of an ethoxylated and/or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 14 or less, preferably 12 or less.
  • Also described is a process for washing articles in a dishwasher comprising the steps of:
  • kits of parts comprising a composition as described above, and instructions stating that no rinse aid or salt is to be added to the dishwashing machine.
  • This invention also relates to the use of 4.0 wt% of an ethoxylated and/or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 12 or less in a dish washing composition, so that the composition can be used in a dishwasher without a separate rinse aid composition (and ideally without separate salt) present in the machine .
  • the surfactant system comprises 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 12°C or less, most preferably 10°C or less.
  • nonionic surfactants having the required cloud points for use in the invention are found in the low- to non-foaming ethoxylated straight-chain alcohols of the Plurafac ® LF series, supplied by the BASF Company; Synperoni ' c RA series supplied by ICI Triton ® DF series, supplied by the Rohm & Haas Company.
  • a suitable nonionic surfactant is SLF 18 B 45, ex. Olin Chemicals. Suitable surfactants must however have the appropriate cloud point .
  • the ethoxylated and/or propoxylated nonionic surfactants are present at levels of at least 4.0 wt%, preferably 4-6 wt%, and in some instances more preferably 5 to 8 wt% of the total composition.
  • An anti-foam to suppress foaming is preferably present
  • an anionic surfactant it is advantageously present at levels of 2 wt% or below.
  • An anti-scaling agent is present in the composition as a preferred feature. It is preferable if the level antiscaling agent is from 0.2 to 10 wt% of the total composition, preferably from 0.5 to 5 wt%.
  • Suitable anti-scaling agents include organic phosphonates, amino carboxylates, polyfunctionally-substituted compounds, and mixtures thereof.
  • 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. Most preferred is hydroxy-ethylene 1,1 diphosphonate (EDHP) and 2 phosphono- butane, 1,2,4 tricarboxylic acid (Bayhibit) .
  • EDHP hydroxy-ethylene 1,1 diphosphonate
  • Bayhibit 1,2,4 tricarboxylic acid
  • water soluble 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 polymers with as monomer units acrylic acid, methyl methacrylic acid, 4-sulfophenyl methylallyl ether and sodium methallyl sulfonate, such as Alcoperse 240 supplied by Alco. ⁇ ; Also suitable is a terpolymer containing polyacrylate with 2-acrylamido-2-methylpropane sulfonic acid such as Acumer 3100 supplied by Rohm & Haas. It is preferable if polymers of this type have a molecular weight from 1,000 to 15,000, more preferably from 3,000 to 10,000.
  • 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.
  • polymeric polycarboxylates are 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.
  • a mixture of anti-scaling agents may be used, particularly useful are a mixture of organic phosphonates and a polymers having as monomer units acrylic acid, methyl methacrylic acid, 4-sulfophenyl methylallyl ether and sodium methallyl sulfonate, Preferred ratios of antiscaling agent to nonionic surfactant are 1:3 to 3:1, more preferably 1:1 to 1:2
  • compositions of the invention may contain a builder.
  • the builder may be a phosphate or non-phosphate builder.
  • compositions of the invention preferably comprise a water- soluble phosphate builder.
  • Phosphate builders are particularly preferred. Specific examples of water-soluble phosphate builders are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta/phosphate in which the degree of polymerisation ranges from about 6 to 21, and salts of phytic acid. Sodium or potassium tripolyphosphate is most preferred.
  • the level of builder is from 50 to 90% by weight, preferably from 55 to 80% by weight.
  • compositions of the present invention may comprise a water-soluble nonphosphate builder.
  • non-phosphorus-containing inorganic builders include water-soluble alkali metal carbonates, bicarbonates, sesquicarbonates, borates, silicates, including layered silicates such as SKS-6 ex. Clarent, metasilicates, and crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite seeds) , potassium carbonate, sodium and potassium bicarbonates, silicates including layered silicates and zeolites .
  • Organic detergent builders can also be used as nonphosphate builders in the present invention.
  • organic builders include alkali metal citrates, succinates, malonates, fatty acid sulfonates, fatty acid carboxylates, nitrilotriacetates, oxydisuccinates, alkyl and alkenyl disuccinates, oxydiacetates, carboxymethyloxy succinates, ethylenediamine tetraacetates, tartrate monosuccinates, tartrate disuccinates, tartrate monoacetates, tartrate diacetates, oxidised starches, oxidised heteropolymeric polysaccharides, polyhydroxysulfonates, polycarboxylates such as polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/ polymethacrylate copolymers, acrylate/maleate/vinyl alcohol terpolymers, aminopolycarboxylates and polyacetal carboxylate
  • Such carboxylates are described in U.S. Patent Nos . 4,144,226, 4,146,495 and 4,686,062.
  • Alkali metal citrates, nitrilotriacetates, oxydisuccinates, acrylate/maleate copolymers and acrylate/maleate/vinyl alcohol terpolymers are especially preferred nonphosphate builders.
  • Silica Silica material may be included in the composition.
  • Suitable forms of silica include amorphous silica, such as precipitated silica, pyrogenic silica and silica gels, such as hydrogels, xerogels and aerogels, or the pure crystal forms quartz, tridymite or crystobalite, but the amorphous forms of silica are preferred.
  • Suitable silicas may readily be obtained commercially. They are sold, for example under the Registered Trade Name Gasil 200 (ex Crosfield, UK) .
  • the silica is in the product in such a form that ⁇ .:> it can dissolve when added to the wash liquor. Therefore, addition of silica by way of addition anti-foam particles of silica and silicone oil is not preferred.
  • silica material are used that have a particle size (as determined with a Malvern Laser, i.e. "aggregated" particles size) of at most 40 ⁇ m, most preferably at most 20 ⁇ m provides better results in the wash.
  • particle size of the silica material is at least l ⁇ m, more preferably at least 2 ⁇ m, most preferably at least 5 ⁇ m.
  • the silica material is present in the cleaning composition at a level of at least 0.1%, more preferably at least 0.5%, most preferably at least 1% by weight of the cleaning composition and preferably at most 10%, more preferably at most 8%, most preferably at most 5% by weight of the cleaning composition.
  • the composition optionally comprises alkali metal silicates.
  • the Si0 2 level should be from 1% to 35%, preferably from 2% to 20%, more preferably from 3% to 10%, based on the weight of the ADD.
  • the alkali metal silicate is hydrous, having from 15% to 25% water, more preferably, from 17% to 20%.
  • the highly alkali metasilicates can in general be employed, although the less alkaline hydrous alkali metal silicates having a Si0 2 :M 2 0 ratio of from 2.0 to 2.4 are, as noted, greatly preferred.
  • Anhydrous forms of the alkali metal silicates with a Si0 2 :M 2 0 ratio of 2.0 or more are also less preferred, because they tend to be significantly less soluble than the hydrous alkali metal silicates having the same ratio.
  • a particularly preferred alkali metal silicate is a granular hydrous sodium silicate having a Si0 2 :Na 2 0 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 Si0 2 :Na 2 0 ratio of 2.0. While typical forms, i.e. powder and granular, of hydrous silicate particles are suitable, preferred silicate particles having a mean particle size between 300 and 900 microns and less than 40% smaller than 150 microns and less than 5% larger than 1700 microns.
  • compositions of the present invention having a pH of 9 or less preferably will be substantially free of alkali metal silicate.
  • 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.
  • 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.
  • amylolytic enzymes the final composition will have amylolytic activity of from 10 2 to 10 e Maltose units/kg.
  • proteolytic enzymes the final composition will have proteolytic enzyme activity of from 10 s to 10 9 Glycine Units/kg.
  • Bleach material is preferably incorporated in the composition.
  • the bleach material may be a chlorine- or bromine-releasing agent or a peroxygen compound. Peroxygen based bleach materials are however preferred.
  • Organic peroxy acids or the precursors therefor are typically utilized as the bleach material.
  • the peroxyacids usable in the present invention are solid and, preferably, substantially water-insoluble compounds.
  • substantially water-insoluble is meant herein a water-solubility of less than about 1% by weight at ambient temperature.
  • peroxyacids containing at least about 7 carbon atoms are sufficiently insoluble in water for use herein.
  • Inorganic peroxygen-generating compounds are also typically used as the bleaching material of the present invention. Examples of these materials are 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) .
  • PAP phthaloyl amido peroxy caproic
  • diperoxy acids useful herein include alkyl diperoxy acids and aryldiperoxy acids, such as 1, 12-di-peroxy- dodecanedioic acid (DPDA) ; 1, 9-diperoxyazelaic acid, diperoxybrassylic acid, diperoxysebacic acid and diperoxy- isophthalic acid; and 2-decyldiperoxybutane-l, 4-dioic acid.
  • DPDA 1, 12-di-peroxy- dodecanedioic acid
  • 1, 9-diperoxyazelaic acid diperoxybrassylic acid, diperoxysebacic acid and diperoxy- isophthalic acid
  • 2-decyldiperoxybutane-l, 4-dioic acid 2-decyldiperoxybutane-l, 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.
  • 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 12.5xl0 "4 % and at most 0.03% avO by weight of the liquor.
  • Anti-tarnishing agents such as benzotriazole 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.
  • buffering 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.
  • Reducing agents may e.g. be used to prevent the appearance of an enzyme-deactivating concentration of oxidant bleach compound.
  • Suitable agents include reducing sulphur-oxy acids and salts thereof.
  • Most preferred for reasons of availability, low cost, and high performance are the alkali metal and ammonium salts of sulphuroxy acids including ammonium sulphite ( (NH 4 ) 2 S0 3 ) , sodium sulphite (Na 2 S0 3 ) , sodium bisulphite (NaHS0 3 ) , sodium metabisulphite (Na 2 S 2 0 3 ) , potassium metabisulphite ( ⁇ S- s ) , lithium hydrosulphite (Li 2 S 2 0 4 ) , etc., sodium sulphite being particularly preferred.
  • Another useful reducing agent 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% to about 1.0% by weight, preferably from about 0.02% to about 0.5% by weight, will be sufficient .
  • compositions according to the invention are preferably processed to be in the form of a tablet, although in some embodiments other product forms (e.g. as a powder) may be contemplated and preferred.
  • the invention relates to washing processes in mechanical dish washing machines wherein the wash liquor has a low pH.
  • low pH is meant here that the pH of the wash liquor is preferably higher than about 6.5, more preferably 7.5 or higher, most preferably 8.5 or higher.
  • the pH is lower than about 11, more preferably lower than about 10.5, more preferably lower than about 9.5.
  • the most advantageous pH range is from 8.5 to 10.5.
  • the plates were removed from the solution and placed in a beaker containing 5 litre of water at 60°C with 15ml of the original solution (this simulates carry over in the rinse cycle, rinse simulation) for 5 minutes.
  • the plates were removed and their contact angle with the rinse solution was measured using a Contact angle Goniometer model A-l 00.
  • Example A Experiment conducted with Example A in the main wash simulation, the rinse simulation and used to measure the contact angle - Treatment A
  • Example 1 diluted as for rinsing procedure (30g in 5 litres of water, diluted by taking 15 ml of this solution and adding to a further 5 litres of water) used to measure the contact angle - Treatment B
  • Example A diluted as for rinsing procedure (30g in 5 litres of water, diluted by taking 15 ml of this solution and adding to a further 5 litres of water) used to measure the contact angle - Treatment C

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)
  • Detergent Compositions (AREA)

Abstract

A machine dish wash composition comprising at least 4.0 wt% of an ethoxylated and/or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 14 or less. The invention also provides a method for washing articles in a dishwasher involving addinng to the wash liquor a composition comprising an ethoxylated and/or propoxylated nonionic surfactant having a cloud point in water of 14 or less and treating the articles to be cleaned with the composition, wherein no additional rinse aid or salt are present in the dishwasher.

Description

DISH-WASHING COMPOSITIONS
The present invention is in the field of machine dishwashing. More specifically, the invention encompasses compositions for use in a machine dish wash formulation, which do not necessitate the addition of salt or rinse aid to the machine .
To wash articles in a commercially available dish washing machine usually entails using three product types. Salt is added to the salt compartment to soften the water, a dishwashing formulation is used to clean the articles, and a rinse aid is used to ensure that the articles are rinsed with no streaks or smears .
Consumers often find it inconvenient replace the salt and rinse aid in a dish wash machine.
WO 00/06684 (Benckiser) discloses a machine dish wash tablet. The tablet has a base composition that carries out it's function in the main wash cycle, and a separate core that acts as a rinse aid in the rinse cycle of the machine. However such a tablet is complicated to manufacture.
WO 95/07330 (Procter & Gamble) and US 5358655 (Henkel) describe dishwashing compositions in which certain well know nonionic surfactants are used- The present invention relates to a composition for washing dishes that obviates the need for salt and rinse aid in the machine dishwashing process .
Accordingly, the present invention relates to a machine dish wash composition comprising at least 4.0 wt% of an ethoxylated and/or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 14 or less, preferably 12 or less.
Also described is a process for washing articles in a dishwasher comprising the steps of:
i) adding a composition as described in the preceding paragraph to the wash liquor of the dish washer followed by;
ii) treating articles requiring cleaning with the wash liquor in a conventional manner;
wherein no additional rinse aid is present within the dishwasher and no salt is present in the dishwasher to rejuvenate the ion exchange.
Also part of this inventive concept is a kit of parts comprising a composition as described above, and instructions stating that no rinse aid or salt is to be added to the dishwashing machine. This invention also relates to the use of 4.0 wt% of an ethoxylated and/or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 12 or less in a dish washing composition, so that the composition can be used in a dishwasher without a separate rinse aid composition (and ideally without separate salt) present in the machine .
Surfactant material
The surfactant system comprises 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 12°C or less, most preferably 10°C or less.
Examples of suitable nonionic surfactants having the required cloud points for use in the invention are found in the low- to non-foaming ethoxylated straight-chain alcohols of the Plurafac® LF series, supplied by the BASF Company; Synperoni'c RA series supplied by ICI Triton® DF series, supplied by the Rohm & Haas Company. A suitable nonionic surfactant is SLF 18 B 45, ex. Olin Chemicals. Suitable surfactants must however have the appropriate cloud point .
The ethoxylated and/or propoxylated nonionic surfactants are present at levels of at least 4.0 wt%, preferably 4-6 wt%, and in some instances more preferably 5 to 8 wt% of the total composition. An anti-foam to suppress foaming is preferably present
If an anionic surfactant is used it is advantageously present at levels of 2 wt% or below.
An i-scaling Agent
An anti-scaling agent is present in the composition as a preferred feature. It is preferable if the level antiscaling agent is from 0.2 to 10 wt% of the total composition, preferably from 0.5 to 5 wt%.
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 α-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. Most preferred is hydroxy-ethylene 1,1 diphosphonate (EDHP) and 2 phosphono- butane, 1,2,4 tricarboxylic acid (Bayhibit) .
Also suitable are water soluble 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 polymers with as monomer units acrylic acid, methyl methacrylic acid, 4-sulfophenyl methylallyl ether and sodium methallyl sulfonate, such as Alcoperse 240 supplied by Alco.~; Also suitable is a terpolymer containing polyacrylate with 2-acrylamido-2-methylpropane sulfonic acid such as Acumer 3100 supplied by Rohm & Haas. It is preferable if polymers of this type have a molecular weight from 1,000 to 15,000, more preferably from 3,000 to 10,000.
As an alternative 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.
Also suitable are polymeric polycarboxylates are 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.
A mixture of anti-scaling agents may be used, particularly useful are a mixture of organic phosphonates and a polymers having as monomer units acrylic acid, methyl methacrylic acid, 4-sulfophenyl methylallyl ether and sodium methallyl sulfonate, Preferred ratios of antiscaling agent to nonionic surfactant are 1:3 to 3:1, more preferably 1:1 to 1:2
Builder, Material
The compositions of the invention may contain a builder.. The builder may be a phosphate or non-phosphate builder.
Compositions of the invention preferably comprise a water- soluble phosphate builder.
Phosphate builders are particularly preferred. Specific examples of water-soluble phosphate builders are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta/phosphate in which the degree of polymerisation ranges from about 6 to 21, and salts of phytic acid. Sodium or potassium tripolyphosphate is most preferred.
The level of builder is from 50 to 90% by weight, preferably from 55 to 80% by weight.
The compositions of the present invention may comprise a water-soluble nonphosphate builder. Suitable examples of non-phosphorus-containing inorganic builders include water-soluble alkali metal carbonates, bicarbonates, sesquicarbonates, borates, silicates, including layered silicates such as SKS-6 ex. Clarent, metasilicates, and crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite seeds) , potassium carbonate, sodium and potassium bicarbonates, silicates including layered silicates and zeolites .
Organic detergent builders can also be used as nonphosphate builders in the present invention. Examples of organic builders include alkali metal citrates, succinates, malonates, fatty acid sulfonates, fatty acid carboxylates, nitrilotriacetates, oxydisuccinates, alkyl and alkenyl disuccinates, oxydiacetates, carboxymethyloxy succinates, ethylenediamine tetraacetates, tartrate monosuccinates, tartrate disuccinates, tartrate monoacetates, tartrate diacetates, oxidised starches, oxidised heteropolymeric polysaccharides, polyhydroxysulfonates, polycarboxylates such as polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/ polymethacrylate copolymers, acrylate/maleate/vinyl alcohol terpolymers, aminopolycarboxylates and polyacetal carboxylates, and polyaspartates and mixtures thereof . Such carboxylates are described in U.S. Patent Nos . 4,144,226, 4,146,495 and 4,686,062. Alkali metal citrates, nitrilotriacetates, oxydisuccinates, acrylate/maleate copolymers and acrylate/maleate/vinyl alcohol terpolymers are especially preferred nonphosphate builders.
Silica Silica material may be included in the composition. Suitable forms of silica include amorphous silica, such as precipitated silica, pyrogenic silica and silica gels, such as hydrogels, xerogels and aerogels, or the pure crystal forms quartz, tridymite or crystobalite, but the amorphous forms of silica are preferred. Suitable silicas may readily be obtained commercially. They are sold, for example under the Registered Trade Name Gasil 200 (ex Crosfield, UK) .
Preferably, the silica is in the product in such a form that ι.:> it can dissolve when added to the wash liquor. Therefore, addition of silica by way of addition anti-foam particles of silica and silicone oil is not preferred.
Therefore, it is preferred that silica material are used that have a particle size (as determined with a Malvern Laser, i.e. "aggregated" particles size) of at most 40μm, most preferably at most 20μm provides better results in the wash. In view of incorporation in a cleaning composition, it is preferred that the particle size of the silica material is at least lμm, more preferably at least 2μm, most preferably at least 5μm.
Preferably, the silica material is present in the cleaning composition at a level of at least 0.1%, more preferably at least 0.5%, most preferably at least 1% by weight of the cleaning composition and preferably at most 10%, more preferably at most 8%, most preferably at most 5% by weight of the cleaning composition.
Silicates
The composition optionally comprises alkali metal silicates. When silicates are present, the Si02 level should be from 1% to 35%, preferably from 2% to 20%, more preferably from 3% to 10%, based on the weight of the ADD. The ratio of Si02 to the alkali metal oxide (M20, where M = alkali metal) is typically from 1 to 3.5, preferably from 1.6 to 3, more preferably from 2 to 2.8. Preferably, the alkali metal silicate is hydrous, having from 15% to 25% water, more preferably, from 17% to 20%.
The highly alkali metasilicates can in general be employed, although the less alkaline hydrous alkali metal silicates having a Si02:M20 ratio of from 2.0 to 2.4 are, as noted, greatly preferred. Anhydrous forms of the alkali metal silicates with a Si02:M20 ratio of 2.0 or more are also less preferred, because they tend to be significantly less soluble than the hydrous alkali metal silicates having the same ratio.
Sodium and potassium, and especially sodium, silicates are preferred. A particularly preferred alkali metal silicate is a granular hydrous sodium silicate having a Si02:Na20 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 Si02:Na20 ratio of 2.0. While typical forms, i.e. powder and granular, of hydrous silicate particles are suitable, preferred silicate particles having a mean particle size between 300 and 900 microns and less than 40% smaller than 150 microns and less than 5% larger than 1700 microns.
Particularly preferred is a silicate particle with a mean particle size between 400 and 700 microns with less than 20% smaller than 150 microns and less than 1% larger then 1700 microns. Compositions of the present invention having a pH of 9 or less preferably will be substantially free of alkali metal silicate.
Enzymes
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.
Well-known and preferred examples of these enzymes are lipases, amylases and proteases. The enzymes most commonly used in machine dishwashing compositions are amylolytic enzymes. Preferably, 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. For amylolytic enzymes, the final composition will have amylolytic activity of from 102 to 10e Maltose units/kg. For proteolytic enzymes the final composition will have proteolytic enzyme activity of from 10s to 109 Glycine Units/kg.
Bleach Material
Bleach material is preferably incorporated in the composition.
The bleach material may be a chlorine- or bromine-releasing agent or a peroxygen compound. Peroxygen based bleach materials are however preferred.
Organic peroxy acids or the precursors therefor are typically utilized as the bleach material. The peroxyacids usable in the present invention are solid and, preferably, substantially water-insoluble compounds. By "substantially water-insoluble" is meant herein a water-solubility of less than about 1% by weight at ambient temperature. In general, peroxyacids containing at least about 7 carbon atoms are sufficiently insoluble in water for use herein. Inorganic peroxygen-generating compounds are also typically used as the bleaching material of the present invention. Examples of these materials are 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) .
Typical diperoxy acids useful herein include alkyl diperoxy acids and aryldiperoxy acids, such as 1, 12-di-peroxy- dodecanedioic acid (DPDA) ; 1, 9-diperoxyazelaic acid, diperoxybrassylic acid, diperoxysebacic acid and diperoxy- isophthalic acid; and 2-decyldiperoxybutane-l, 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.
If desirably 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 , is to be incorporated, this may be presented in the form of a second encapsulate separately from the bleach capsule or granule. Cobalt catalysts can also be used.
For peroxygen bleaching agents a suitable range is also from 0.5% to 3% avO (available Oxygen). Preferably, the amount of bleach material in the wash liquor is at least 12.5xl0"4% and at most 0.03% avO by weight of the liquor.
Anti-tarnishing Agents.
Anti-tarnishing agents such as benzotriazole and those described in EP 723 577 (Unilever) may also be included.
Optional Ingredients
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.
Reducing agents may e.g. be used to prevent the appearance of an enzyme-deactivating concentration of oxidant bleach compound. Suitable agents include reducing sulphur-oxy acids and salts thereof. Most preferred for reasons of availability, low cost, and high performance are the alkali metal and ammonium salts of sulphuroxy acids including ammonium sulphite ( (NH4) 2S03) , sodium sulphite (Na2S03) , sodium bisulphite (NaHS03) , sodium metabisulphite (Na2S203) , potassium metabisulphite ( ^S- s) , lithium hydrosulphite (Li2S204) , etc., sodium sulphite being particularly preferred. 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% to about 1.0% by weight, preferably from about 0.02% to about 0.5% by weight, will be sufficient .
Compositions according to the invention are preferably processed to be in the form of a tablet, although in some embodiments other product forms (e.g. as a powder) may be contemplated and preferred.
pH of wash liquor
The invention relates to washing processes in mechanical dish washing machines wherein the wash liquor has a low pH. By "low pH" is meant here that the pH of the wash liquor is preferably higher than about 6.5, more preferably 7.5 or higher, most preferably 8.5 or higher. Preferably the pH is lower than about 11, more preferably lower than about 10.5, more preferably lower than about 9.5. The most advantageous pH range is from 8.5 to 10.5.
The invention will now be illustrated by the following non- limiting Examples. All percentages are on a weight basis,
Table 1
1) acrylic acid polymer ex BASF
2) Nonionic surfactant, ex BASF (LF 403)
Spot formation on glassware is a primary reason why rinse aids are added to dish washing machines. It has been found that the contact angles on glass correlate very well with spot scores on glasses. Experiments having low spot scores (that is few deposits on glasses, so better results) were found when contact angles were also low (less than 20) . 8 glass plates were subjected to the following treatment to simulate their washing in the dish washer. They were placed in a rack which was placed in a beaker containing 5 litres of water (40 FH) at 60°C, 30g of composition to be tested and 3g of egg yolk. The plates were kept in this stirred solution for 45 minutes at 60°C (main wash simulation) . The plates were removed from the solution and placed in a beaker containing 5 litre of water at 60°C with 15ml of the original solution (this simulates carry over in the rinse cycle, rinse simulation) for 5 minutes. The plates were removed and their contact angle with the rinse solution was measured using a Contact angle Goniometer model A-l 00.
Various treatments were used:
Experiment conducted with Example 1 in the main wash simulation, the rinse simulation and used to measure the contact angle - Treatment 1
Experiment conducted with Example A in the main wash simulation, the rinse simulation and used to measure the contact angle - Treatment A
To demonstrate that the contact angle was influenced by the washing process and not merely the rinse solutions used to measure the contact angles, plates were placed in 60°C water with no added product for 60 minutes. The contact angle in the rinse solution was measured.
Experiment conducted with water in the main wash simulation and the rinse simulation, Example 1 diluted as for rinsing procedure (30g in 5 litres of water, diluted by taking 15 ml of this solution and adding to a further 5 litres of water) used to measure the contact angle - Treatment B
Experiment conducted with water in the main wash simulation and the rinse simulation, Example A diluted as for rinsing procedure (30g in 5 litres of water, diluted by taking 15 ml of this solution and adding to a further 5 litres of water) used to measure the contact angle - Treatment C
The results are as follows:
Contact angle (average) Treatment 1 8 Treatment A 27
Treatment B 28
Treatment C 33.

Claims

1. A process for washing articles in a dishwasher comprising the steps of: i) adding a composition comprising at least 4% by weight of an ethoxylated and/or propoxylated nonionic surfactant which has a cloud point in water of 14 or less to the wash liquor of the dish washer followed by; ii) treating articles requiring cleaning with the wash liquor in a conventional manner; wherein no additional rinse aid is present within the dishwasher.
2. A process according to claim 1 wherein no salt is added to the dishwasher to rejuvenate the ion exchange.
3. A process according to claim 1 or claim 2 in which the level of nonionic surfactant is from 4% to 8%, preferably from 5% to 8 wt% of the total composition.
. A process according to any of the preceding claims in which the nonionic surfactant is selected from nonionic surfactants having a cloud point in water of 12 or less.
5. A process according to any of the preceding claims, which further comprises an anti-scaling agent in the composition.
6. A process according to claims 5 in which the level of antiscaling agent in the composition is from 0.5 to 5 wt%.
7. A process according to any of the preceding claims wherein the composition comprises greater than 50 wt% of a builder.
8. A process according to claim 7 in which the builder is a water-soluble phosphate.
9. A process according to any of the preceding claims in which the composition is in the form of a tablet.
10. A machine dish wash composition comprising at least 4.0 wt% of an ethoxylated or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 14 or less, the composition being provided together with instructions not to include a rinse aid in the machine dishwashing process.
11. A machine dishwashing composition according to claim 10 provided together with instructions not to include salt in the machine dishwashing process.
12. A machine dish wash composition according to claim 10 or claim 11 in which the level of nonionic surfactant is from 4% to 8%, preferably 5% to 8 wt% of the total composition.
13. A machine dish wash composition according to any one of claims 11 to 13 in which the nonionic surfactant is selected from nonionic surfactants having a cloud point in water of 12 or less.
14. A machine dish wash composition according to any one of claims 10 to 13, which further comprises an anti- scaling agent.
15. A machine dish wash composition according to claim 14 in which the level of antiscaling agent is from 0.5 to 5 wt%.
16. A machine dish wash composition according to any one co claims 10 to 15 comprising greater than 50wt% of a builder.
17. A machine dish wash composition according to claim 16 in which the builder is a water-soluble phosphate.
18. A machine dish wash composition according to any one of claims 10 to 17 in which the composition is in the form of a tablet.
19. A kit of parts comprising:
(i) a composition as claimed in any one of claims 10 to 18 and; (ii) instructions stating that no rinse aid or salt is to be added to the dishwashing machine
20. Use of at least 4.0 wt% of an ethoxylated and/or propoxylated nonionic surfactant in which the nonionic surfactant has a cloud point in water of 14 or less in a dish washing composition so that the composition can be used in a dishwasher without a separate rinse aid composition being present in the machine.
21. Use according to claim 20 wherein the composition can be used in a dishwasher without separate salt being present in the machine.
EP01982443A 2000-10-25 2001-10-18 Dish-washing compositions Expired - Lifetime EP1328611B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP01982443A EP1328611B1 (en) 2000-10-25 2001-10-18 Dish-washing compositions

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP00309394 2000-10-25
EP00309394 2000-10-25
EP01982443A EP1328611B1 (en) 2000-10-25 2001-10-18 Dish-washing compositions
PCT/EP2001/012351 WO2002034869A1 (en) 2000-10-25 2001-10-18 Dish-washing compositions

Publications (2)

Publication Number Publication Date
EP1328611A1 true EP1328611A1 (en) 2003-07-23
EP1328611B1 EP1328611B1 (en) 2005-12-28

Family

ID=8173339

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01982443A Expired - Lifetime EP1328611B1 (en) 2000-10-25 2001-10-18 Dish-washing compositions

Country Status (6)

Country Link
EP (1) EP1328611B1 (en)
AR (1) AR031043A1 (en)
AT (1) ATE314448T1 (en)
AU (1) AU2002214027A1 (en)
DE (1) DE60116358T2 (en)
WO (1) WO2002034869A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2491842B1 (en) 2011-02-22 2017-01-25 Miele & Cie. KG Method of performing a washing program

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7285171B2 (en) 2002-12-19 2007-10-23 The Procter & Gamble Company Anti-filming materials, compositions and methods

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2552506A1 (en) * 1975-11-22 1977-05-26 Henkel & Cie Gmbh MACHINE APPLICABLE COMBINED DISHWASHER AND RINSE AID AND PROCESS FOR SIMULTANEOUSLY CLEANING AND RINSE DISHWASHER IN DISHWASHER
US4306987A (en) * 1979-11-19 1981-12-22 Basf Wyandotte Corporation Low-foaming nonionic surfactant for machine dishwashing detergent
GB8721936D0 (en) * 1987-09-18 1987-10-28 Rohm & Haas Composition
DE4110510A1 (en) * 1991-03-30 1992-10-01 Henkel Kgaa LOW-ALKALINE, CHLORINE AND PHOSPHATE-FREE MACHINE DISTRIBUTORS IN THE FORM OF HEAVY-DENTAL POWDERS AND GRANULES
DE4112075A1 (en) * 1991-04-12 1992-10-15 Henkel Kgaa METHOD FOR PRODUCING STABLE, BIFUNCTIONAL, PHOSPATE AND METASILICATE-FREE LOW-ALKALINE DETERGENT TABLETS FOR THE MACHINE DISHWASHER
EP0717766B1 (en) * 1993-09-09 1998-04-01 The Procter & Gamble Company Automatic dishwashing detergent with alkoxy or aryloxy amide surfactant
DE19518693A1 (en) * 1995-05-22 1996-11-28 Henkel Kgaa Automatic dishwashing detergent with silver corrosion inhibitor
ATE254162T1 (en) * 1996-09-11 2003-11-15 Procter & Gamble LOW-FOAMING MACHINE DISHWASHING DETERGENT
JP2000502750A (en) * 1996-09-11 2000-03-07 ザ、プロクター、エンド、ギャンブル、カンパニー Detergent composition
US5876514A (en) * 1997-01-23 1999-03-02 Ecolab Inc. Warewashing system containing nonionic surfactant that performs both a cleaning and sheeting function and a method of warewashing
WO1999041349A1 (en) * 1998-02-17 1999-08-19 Agency Design Services Limited A cleaning and coating composition for glass, ceramic and metal surfaces
DE19834180A1 (en) * 1998-07-29 2000-02-03 Benckiser Nv Composition for use in a dishwasher
AU2110500A (en) * 1999-02-05 2000-08-25 Unilever Plc Dish washing process and compositions relating thereto
GB2346319B (en) * 1999-02-05 2002-12-04 Unilever Plc A machine dishwashing kit

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0234869A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2491842B1 (en) 2011-02-22 2017-01-25 Miele & Cie. KG Method of performing a washing program

Also Published As

Publication number Publication date
AU2002214027A1 (en) 2002-05-06
WO2002034869A1 (en) 2002-05-02
DE60116358T2 (en) 2006-06-22
EP1328611B1 (en) 2005-12-28
ATE314448T1 (en) 2006-01-15
DE60116358D1 (en) 2006-02-02
AR031043A1 (en) 2003-09-03

Similar Documents

Publication Publication Date Title
EP1721962B1 (en) Dishwashing composition and process for washing dishes
US6239091B1 (en) Machine dishwashing compositions with a polymer having cationic monomer units
EP0998548B1 (en) Automatic dishwashing compositions containing water soluble cationic or amphoteric polymers
JP3984287B2 (en) Detergent compositions and methods for dishwashing
EP0770121B1 (en) Washing process and composition
US5705465A (en) Anti-foam system for automatic dishwashing compositions
EP1328613B1 (en) Dish-washing compositions
WO2021016633A1 (en) Automatic dishwashing detergent composition
EP1328611B1 (en) Dish-washing compositions
CA2327308A1 (en) Machine dishwashing compositions and rinse aid compositions
US6463939B1 (en) Dish washing process
JPH01146996A (en) Phosphorus free washing bleaching agent composition
WO2019032281A1 (en) Automatic dishwashing composition
EP1111037B1 (en) Use of dish-washing compositions
US6310023B1 (en) Machine dish wash compositions
EP0463801A2 (en) Composition and method for fabric encrustation prevention
BE1013471A3 (en) USE OF dishwashing.
ZA200105695B (en) Dish washing process and compolsitions relating thereto.
EP1190029A1 (en) Dish washing process and compositions relating thereto
WO2001002524A1 (en) Dish washing compositions
EP0463802A1 (en) Composition and method of fabric encrustation prevention
EP1287107A1 (en) Dish washing compositions

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: 20030314

AK Designated contracting states

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

17Q First examination report despatched

Effective date: 20031120

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

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

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20051228

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: 20051228

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: 20051228

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

Owner name: UNILEVER N.V.

Owner name: UNILEVER PLC

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

REF Corresponds to:

Ref document number: 60116358

Country of ref document: DE

Date of ref document: 20060202

Kind code of ref document: P

REG Reference to a national code

Ref country code: CH

Ref legal event code: NV

Representative=s name: E. BLUM & CO. PATENTANWAELTE

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: 20060328

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: 20060328

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: 20060328

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 FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20060408

RAP2 Party data changed (patent owner data changed or rights of a patent transferred)

Owner name: UNILEVER PLC

Owner name: UNILEVER N.V.

ET Fr: translation filed
NLT2 Nl: modifications (of names), taken from the european patent patent bulletin

Owner name: UNILEVER N.V.

Effective date: 20060719

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

Ref country code: PT

Payment date: 20061006

Year of fee payment: 6

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: 20061018

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

Ref country code: CH

Payment date: 20061027

Year of fee payment: 6

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: 20061031

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

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

Ref country code: LU

Payment date: 20061107

Year of fee payment: 6

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

Ref country code: BE

Payment date: 20061124

Year of fee payment: 6

26N No opposition filed

Effective date: 20060929

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

Ref country code: DE

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

Effective date: 20070501

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

REG Reference to a national code

Ref country code: CH

Ref legal event code: PFA

Owner name: UNILEVER N.V.

Free format text: UNILEVER N.V.#WEENA 455#3013 AL ROTTERDAM (NL) -TRANSFER TO- UNILEVER N.V.#WEENA 455#3013 AL ROTTERDAM (NL)

BERE Be: lapsed

Owner name: *UNILEVER N.V.

Effective date: 20071031

REG Reference to a national code

Ref country code: PT

Ref legal event code: MM4A

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

Effective date: 20080418

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: LI

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

Effective date: 20071031

Ref country code: CH

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

Effective date: 20071031

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: 20051228

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: 20080418

Ref country code: BE

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

Effective date: 20071031

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: 20051228

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: 20071018

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 15

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 16

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

Ref country code: NL

Payment date: 20161019

Year of fee payment: 16

Ref country code: GB

Payment date: 20161020

Year of fee payment: 16

Ref country code: FR

Payment date: 20161020

Year of fee payment: 16

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

Ref country code: IT

Payment date: 20161024

Year of fee payment: 16

REG Reference to a national code

Ref country code: NL

Ref legal event code: MM

Effective date: 20171101

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

Effective date: 20171018

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20180629

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: 20171101

Ref country code: GB

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

Effective date: 20171018

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: 20171031

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: 20171018