EP1751265A1 - Paste-like concentrate suitable to form stable (non seperating) alkaline cleaning and detergent solutions - Google Patents

Paste-like concentrate suitable to form stable (non seperating) alkaline cleaning and detergent solutions

Info

Publication number
EP1751265A1
EP1751265A1 EP04741679A EP04741679A EP1751265A1 EP 1751265 A1 EP1751265 A1 EP 1751265A1 EP 04741679 A EP04741679 A EP 04741679A EP 04741679 A EP04741679 A EP 04741679A EP 1751265 A1 EP1751265 A1 EP 1751265A1
Authority
EP
European Patent Office
Prior art keywords
concentrate
general formula
mpas
whole
concentrate according
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
EP04741679A
Other languages
German (de)
French (fr)
Other versions
EP1751265B1 (en
Inventor
Khalil Shamayeli
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.)
Ecolab Inc
Original Assignee
Ecolab Inc
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 Ecolab Inc filed Critical Ecolab Inc
Publication of EP1751265A1 publication Critical patent/EP1751265A1/en
Application granted granted Critical
Publication of EP1751265B1 publication Critical patent/EP1751265B1/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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/044Hydroxides or bases
    • 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
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • 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
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/003Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/08Silicates
    • 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
    • C11D1/722Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups

Definitions

  • Paste-like concentrate suitable to form stable (non separating) alkaline cleaning and detergent solutions
  • the present invention refers to a paste-like thixotropic detergent or cleaning concentrate which is able to form a stable (non separating) alkaline parent lye for use as cleansing agent or detergent, preferably for the machine cleaning of textiles, a parent lye containing said concentrate and to a method for washing textiles using said concentrate in diluted form as a parent lye.
  • the single washing machines are centrally supplied with the solution of a detergent or cleaning agent, the so called parent lye, to maximize the capacity of the laundry and the machinery and to optimise the course of the process.
  • the central supply proceeds using a parent lye which contains 5 to 15 wt.-% of the cleaning agent or detergent and which is distributed from a reservoir to the single washing machines, in most cases without further diluting.
  • a cleaning agent or detergent suitable for use in industrial laundries must be capable to form a stable (non separating) alkaline cleaning or detergent solution to ensure a constantly excellent cleaning or washing performance.
  • the object of the present invention is to provide a cleaning or detergent concentrate which on one hand forms a stable paste as such and on the other hand also forms a stable (non separating) alkaline cleaning or detergent solution when dissolved in water. Additionally, it should be possible to purify waste water resulting from the cleaning or washing process and containing said concentrate on common membrane filtration units, especially ones using one or more reverse osmosis steps, without blocking the membrane or causing other damages.
  • a paste-like, thixotropic, alkaline detergent or cleaning concentrate comprising a) at least one first component selected from one or more compounds represented by the general formula (I), R -(OC 2 H 4 ) n -(OC 3 H 6 ) m -OH (I) wherein R 1 represents an unbranched or branched alkyl or alkenyl group having 4 to 8, preferably 5 to 7, carbon atoms, and wherein the sum of the average degree of ethoxylation n and propoxylation m ranges from 1 to 9, preferably from 3 to 7, with one of n and m optionally being 0, and b) at least one second component selected from one or more compounds represented by the general formula (II),
  • thixotropic means that the concentrate exhibits such a structural viscosity that it does not flow under the influence of gravity.
  • the dosing of thixotropic composition is then preferably performed by shearing the concentrate to reduce viscosity at first and afterwards dosing and transmitting the free-flow concentrate using for example a feed pump.
  • the above mentioned viscosity values refer to read- ing after a detection time of 3 minutes to take the time dependency of the thixotropic effect into account.
  • the decrease of viscosity on shear is to a great extent reversible, i. e. after having stopped the shear the concentrate will return to its original physical condition without separation.
  • the viscosity may change while an equilibrium adjusts within the concentrate after its preparation. Accordingly, viscosity values measured during the manufacturing process or directly afterwards may falsify the result. Thus, the viscosities are determined after the equilibrium is adjusted and the final viscosity is reached. Storing for one month is generally sufficient to obtain reliable values.
  • a mixture of two or more compounds represented by general formula II is used wherein R 2 is C10, C13 and/or C12-14, o is 3, 4 and/or 5 and p is 0 or 5. In these cases it is especially preferred to use at least one compound represented by the general formula I wherein R 1 is C6, n is 5 and m is 0.
  • the preferred amount of the com ⁇ ound(s) represented by the general formula (I) is in the range of from 0,5 to 15 wt.-%, preferably 1 to 10 wt.-% and most preferred from 2 to 5 wt.-% based on the whole concentrate.
  • the one or more compounds represented by the general formula (II) should be present in an amount of from 5 to 90 wt.-%, preferably from 15 to 70 wt.-% and most pre- ferred from 20 to 50 wt.-% based on the whole concentrate.
  • the alkalinity may be achieved using any compound known in the state of the art which when dissolved in water shows an alkaline reaction, like for example alkali hydroxides, especially sodium or potassium hydroxide, ammoniumhydroxide, alkaline-earth hydrox- ides, alkali carbonates, like soda or mixtures thereof.
  • alkali hydroxides especially sodium or potassium hydroxide, ammoniumhydroxide, alkaline-earth hydrox- ides, alkali carbonates, like soda or mixtures thereof.
  • the preferred alkalinity generating compound is represented by soda.
  • amorphous alkali silicate may be added as alkalinity source.
  • Sodium meta silicate with a ratio of Na 2 O : Si0 2 in the range of 1 : 0,8 to 1 : 1 ,3, preferably 1 : 1 is especially appropriate.
  • one or more phosphates can be used instead of or in addition to the amorphous alkali silicate.
  • the phosphates are preferably selected from at least one of primary ortho- phosphates represented by the general formula M'H 2 P0 4 or M"(H 2 P0 4 ) 2 , secondary ortho- phosphates represented by the general formula M' 2 HP0 4 or M ⁇ HPO 4 or tertiary orthophos- phates represented by the general formula M' 3 PO or M" 3 (P0 ) 2 , as well as condensed phosphates derived therefrom, the so called meta phosphates and poly phosphates, with M being a metal cation , M 1 preferably being an alkali metal and M" preferably being an alkaline-earth metal.
  • the phosphate is a tripolyphosphate, preferably sodium tripolyphosphate (NasP ⁇ Oio).
  • the content of the alkalinity source is chosen such that the pH value of a use solution containing the inventive concentrate should advantageously be in the range of from 9 to 13, preferably 10 to1 .
  • the total amount of the alkalinity source pref- erably ranges from 25 to 70 wt.-%, more preferably from 30 to 60 wt.-% and most preferred from 50 to 58 wt.-%, based on the whole concentrate.
  • soda is used in amounts of from 15 to 60 wt.-%, preferably 25 to 55 wt.-%.
  • the amount of amorphous alkali silicate, especially sodium meta silicate, with the above mentioned Na 2 0 : Si0 2 ratio preferably ranges from 10 to 20 wt.-%, and especially is 15 wt.-%.
  • the phosphor compound should be contained in an amount of at most 40 wt.-%, preferably in an amount of 30 wt.-% or below, especially in a range of from 20 to 30 wt.-% based on the whole concentrate.
  • the inventive concentrate may additionally comprise at least 1 wt.-% based on the whole concentrate of at least one alkanolamine.
  • the sum of alkanolamines contained in the concentrate is contained in an amount above 2 wt.-% and lies within the range of from 2 to 10 wt.-%, and in particular from 3 to 5 wt.-%, based on the whole concentrate.
  • At least one of the alkanolamines is represented by the general formula (III),
  • R 3 represents a hydroxyalkyl group having 1 to 6 carbon atoms, and wherein R 4 and R 5 independent from each other are identical with R 3 or represent hydrogen.
  • the most suitable alkanolamines are represented by mono-, di- or triethanolamine or mixtures thereof.
  • alkanolamines may function as solutizer and thus improve the homogeneity of the inventive concentrate when diluted to form the use solution, for example the parent lye.
  • alkanolamines additionally represent an alkalinity source. As they are liquid they help to avoid the use of water to provide the paste-like concentrate.
  • the paste-like concentrate comprises a solid phase which is dispersed in a liquid phase as homogeneous as possible.
  • the composition according to the present invention forming the above concentrate enables the water content to be reduced to an amount preferably of less than 3 wt.-%, more preferred less than 2 wt.-%, and most preferred less than 1 wt-% based on the whole concentrate.
  • Said water content is meant to refer to free water only. Additional water may be present in form of water of crystallisation or water of constitution.
  • the concentrate may additionally comprise dehydration agents, for example in form of salts which bind water of crystallisation like anhydrous sodium acetate, calcium sulfate, calcium chloride, sodium hydroxide, magnesium silicate or metal oxides like CaO, MgO, P 4 O ⁇ 0 or Al 2 0 3 or mixtures thereof.
  • dehydration agents for example in form of salts which bind water of crystallisation like anhydrous sodium acetate, calcium sulfate, calcium chloride, sodium hydroxide, magnesium silicate or metal oxides like CaO, MgO, P 4 O ⁇ 0 or Al 2 0 3 or mixtures thereof.
  • the concentrate may additionally contain at least one alkyl polyglucoside having from 8 to 14 carbon atoms in the alkyl group and from 1 to 5 glucose moieties.
  • the amount of the alkyl polyglucosid should be in the range of from 1 to 6 wt.%, preferably from 1,5 to 3 wt.%.
  • Such compounds have a strongly hydrophobic alkyl moiety and a strongly hy- drophilic glucosid moiety and, accordingly, are very much appropriate to function as stabilizer of the paste-like concentrate.
  • the concentrate may comprise one or more further additives generally used in cleaning agents or detergents like further soil release agents, cobuilders, optical brighteners, dyes and fragrances, small quantities of neutral salts such as sulfates and chlorides in the form of their sodium or potassium salts, provided that these do not impair the positive properties.
  • suitable additives to the product may be enzymes, foam regulators, redeposition inhibitors, soil release agents, bleaching agents from the class of per com- pounds, which are conventionally used together with activators, active chlorine compounds as well as dyes, dye transfer inhibitors or dye intensifiers and fragrances.
  • liquid components should be pre-mixed before the solid components and further ingredients are incorporated.
  • particulate solids are not fine enough to provide a homogeneous, paste-like concentrate, they may be grinded one or more times before incorporation.
  • the inventive concentrate as described above can be used to prepare a stable parent lye.
  • the parent lye contains the inventive concentrate in amounts of from 0,5 to 25 wt.-%, preferably 5 to 15 wt.-% based on the detergent solution.
  • the concentrate is dissolved in pure water to form the parent lye.
  • further additives like hydrophilic auxiliaries, are dissolved.
  • the main emphasis for the usage of the concentrate or the solution containing the inventive concentrate, respectively, is on laundry detergents, it may as well be applied as cleaning agent in warewashing, clean in place cleaners and sanitizers, food an dairy formulations and other applications in which such alkaline cleaning solutions may be applied.
  • the solution containing the concentrate is used as parent lye for the industrial machine cleaning of textiles.
  • the present invention provides a method for washing textiles comprising one step in which a parent lye is prepared by diluting the concentrate according to claims 1 to 12 such that the parent lye contains the concentrate in an amount of from 0,5 to 25 wt.-%, preferably of from 5 to 15 wt.-% based on the detergent solution.
  • the concentrate according to the invention is metered from a storage reservoir using a metering equipment which is suitable to meter paste-like substances by influence of shearing force.
  • An appropriate equipment is described for example in WO 95/09263.
  • the required amount of the concentrate which then is free-flow is transmitted into a further tank in which it is combined and dissolved with the appropriate amount of solvent, which generally is water and may as well contain further additives or auxiliaries.
  • the mixture is advantageously agitated.
  • the resulting parent lye may than either directly be distributed to the single washing machines or stored for usage in washing cycles to be performed later.
  • the parent lye is shortly agitated after having been stored before it is distributed to the single washing machines to guarantee a homogeneous distribution of the active agent in the parent lye.
  • the parent lye may be further diluted depending on the desired detergent concentration.
  • the paste-like concentrate for example to wrap it in foil bags. Since the concentrate essentially does not contain water the concentrate may be wrapped in foils which are water soluble. In this case when preparing the parent lye the required number of foil bags is poured into a tank, the appropriate amount of water is added and after the foils are dissolved by the water the parent lye may be obtained by stirring.
  • a further advantage resulting from the composition of the concentrate is that it allows the purification of the waste water which is accumulated during the cleaning or wash- ing process using common membrane filtration units without blocking them or causing other damages.
  • the membrane filtration may as well comprise at least one ultra filtration and/or reverse osmosis step. Said purification processes succeed best with a concentrate according to the invention which contains one or more phosphates.
  • the cited values refer to wt.-%, based on the whole concentrate.
  • the paste-like concentrates exhibited good storage stabilities, i. e. they did not separate over a period of at least 12 months, provided stable parent lyes when being stirred and optionally warmed up to 30-40°C, i. e. they essentially did not separate over a period of at least 1 week, when diluted in water in an amount such that the content of the concentrate was 10 wt.-% based on the parent lye. Generally, slightly stirring was sufficient to obtain a stable parent lye. Moreover, the concentrate when used as a 10 wt.-% aqueous parent lye exhibited excellent cleaning properties.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The present invention refers to a paste-like, thixotropic, alkaline detergent or cleaning concentrate comprising a) at least one first component selected from one or more compounds represented by the general formula (I): R<1>-(OC2H4)n-(OC3H6)m-OH wherein R<1> represents an unbranched or branched alkyl or alkenyl group having 4 to 8, preferably 5 to 7, carbon atoms, and wherein the sum of the average degree of ethoxylation n and propoxylation m ranges from 1 to 9, preferably from 3 to 7, with one of n and m optionally being 0, and b) at least one second component selected from one or more compounds repre­sented by the general formula (II): R<2>-(OC2H4)0-(OC3H6)p-OH wherein R<2>represents an unbranched or branched alkyl or alkenyl group having 9 to 22, preferably 10 to 16, carbon atoms, and wherein the sum of the average degree of ethoxylation o and propoxylation p is between 1 and 9, preferably between 3 and 7, with one of o or p optionally being 0, the cleaning concentrate exhibiting at 25°C a viscosity of from 80 000 mPas to 250 000 mPas at 5 revolutions per minute and a viscosity of from 20 000 mPas to 80 000 mPas at 50 revolutions per minute, each measured using a Brookfield rotational viscometer (spindle no. 7) under otherwise identical conditions. Moreover, it deals with a stable parent lye containing said concentrate and a method for washing textiles comprising one step in which a parent lye is prepared by diluting said concentrate and in 30 which the waste water accumulated during the whole washing process or parts thereof may be purified using a membrane filtration unit.

Description

Paste-like concentrate suitable to form stable (non separating) alkaline cleaning and detergent solutions
[0001] The present invention refers to a paste-like thixotropic detergent or cleaning concentrate which is able to form a stable (non separating) alkaline parent lye for use as cleansing agent or detergent, preferably for the machine cleaning of textiles, a parent lye containing said concentrate and to a method for washing textiles using said concentrate in diluted form as a parent lye.
[0002] In industrial laundries nowadays the single washing machines are centrally supplied with the solution of a detergent or cleaning agent, the so called parent lye, to maximize the capacity of the laundry and the machinery and to optimise the course of the process. Generally , the central supply proceeds using a parent lye which contains 5 to 15 wt.-% of the cleaning agent or detergent and which is distributed from a reservoir to the single washing machines, in most cases without further diluting. Accordingly, a cleaning agent or detergent suitable for use in industrial laundries must be capable to form a stable (non separating) alkaline cleaning or detergent solution to ensure a constantly excellent cleaning or washing performance.
[0003] Cleaning and detergent compositions formulated in particulate form are well known to form stable (non separating) alkaline cleaning or detergent solutions. However, generally large amounts of parent lye are prepared and stored in a reservoir to be subsequently distributed to the single washing machines. This means a corresponding amount of solid detergent or cleaning agent, respectively, has to be dissolved to form the parent lye, which takes a lot of time and effort.
[0004] Moreover, large amounts of solid, especially particulate, detergents show problems with respect to homogeneity if they are stored before being used to form the parent lye and not consumed at one go. This is because the single components in the detergent exhibit different volumes and densities which results in the active components migrating to the bottom of the reservoir upon storage. Accordingly, if the parent lyes are prepared using a detergent powder stored in a reservoir, this migrating process may take place therein while consuming the parent lye. The following parent lyes may then exhibit a more and more decreased cleaning performance due to the more and more decreasing content of active agent in the solid detergent. The parent lye formed from the detergent on the bottom of the reservoir, where the active ingredient accumulated, then again exhibits excellent cleaning performance. [0005] Accordingly there is a need to provide stable homogenous paste-like detergent or cleaning concentrates which are easily batched and dissolved to form a stable parent lye and exhibit excellent cleaning properties, especially in laundry application.
[0006] Yet, the actually known paste-like detergent and cleaning concentrates do not exhibit this combination of properties. In particular, a large amount of a non-ionic surfactant blend is required as liquid component to provide those concentrates with a viscid to highly viscous consistency. Accordingly, when forming a parent lye, those concentrates generally show poor solubility and do not form stable (non separating) solutions. Even the use of emul- sifiers in large amounts which increases costs and complicates the disposal of the resulting waste water, did not provide a homogenous, stable parent lye. This results in the requirement of vigorous stirring in the vessel during storage of the parent lye to ensure a more or less homogenous distribution of the detergent concentrate. In most cases not even vigorous stirring provides a homogenous parent lye.
[0007] Moreover, nowadays it is very important to provide cleaning agents and detergents which do not only exhibit excellent cleaning properties but which are as well accessible to the common waste water purification systems. If the waste water and/or a part of the de- tergent solution accumulating after the washing process has been carried out is treated by membrane filtration, many non-ionic surfactants cause considerable problems. Depending on the choice of non-ionic surfactant, this may even lead to blocking-up of the membranes. This point is to be deemed particularly critical in membrane filtration processes in the course of which at least one reverse osmosis step occurs.
[0008] Therefore, the object of the present invention is to provide a cleaning or detergent concentrate which on one hand forms a stable paste as such and on the other hand also forms a stable (non separating) alkaline cleaning or detergent solution when dissolved in water. Additionally, it should be possible to purify waste water resulting from the cleaning or washing process and containing said concentrate on common membrane filtration units, especially ones using one or more reverse osmosis steps, without blocking the membrane or causing other damages.
[0009] Surprisingly, the underlying problem is solved by providing a paste-like, thixotropic, alkaline detergent or cleaning concentrate comprising a) at least one first component selected from one or more compounds represented by the general formula (I), R -(OC2H4)n-(OC3H6)m-OH (I) wherein R1 represents an unbranched or branched alkyl or alkenyl group having 4 to 8, preferably 5 to 7, carbon atoms, and wherein the sum of the average degree of ethoxylation n and propoxylation m ranges from 1 to 9, preferably from 3 to 7, with one of n and m optionally being 0, and b) at least one second component selected from one or more compounds represented by the general formula (II),
R2-(OC2H4)o-(OC3H6)p-OH (II) wherein R2 represents an unbranched or branched alkyl or alkenyl group having 9 to 22, preferably 10 to 16, carbon atoms, and wherein the sum of the average degree of ethoxylation o and propoxylation p ranges from 1 to 9, preferably from 3 to 7, with one of o or p optionally being 0, the cleaning concentrate exhibiting at 25°C a viscosity of from 80000 mPas to 250 000 mPas at 5 revolutions per minute and a viscosity of from 20 000 mPas to 80 000 mPas at 50 revolutions per minute, each measured using a Brookfield rotational viscometer (spindle no. 7) under otherwise identical conditions.
[0010] In this context thixotropic means that the concentrate exhibits such a structural viscosity that it does not flow under the influence of gravity. However, on shear the viscosity tremendously decreases which enables the concentrate to flow under the influence of gravity. The dosing of thixotropic composition is then preferably performed by shearing the concentrate to reduce viscosity at first and afterwards dosing and transmitting the free-flow concentrate using for example a feed pump. The above mentioned viscosity values refer to read- ing after a detection time of 3 minutes to take the time dependency of the thixotropic effect into account. The decrease of viscosity on shear is to a great extent reversible, i. e. after having stopped the shear the concentrate will return to its original physical condition without separation.
[0011] It has to be taken into account that the viscosity may change while an equilibrium adjusts within the concentrate after its preparation. Accordingly, viscosity values measured during the manufacturing process or directly afterwards may falsify the result. Thus, the viscosities are determined after the equilibrium is adjusted and the final viscosity is reached. Storing for one month is generally sufficient to obtain reliable values.
[0012] In a preferred embodiment a mixture of two or more compounds represented by general formula II is used wherein R2 is C10, C13 and/or C12-14, o is 3, 4 and/or 5 and p is 0 or 5. In these cases it is especially preferred to use at least one compound represented by the general formula I wherein R1 is C6, n is 5 and m is 0.
[0013] The preferred amount of the comρound(s) represented by the general formula (I) is in the range of from 0,5 to 15 wt.-%, preferably 1 to 10 wt.-% and most preferred from 2 to 5 wt.-% based on the whole concentrate.
[0014] The one or more compounds represented by the general formula (II) should be present in an amount of from 5 to 90 wt.-%, preferably from 15 to 70 wt.-% and most pre- ferred from 20 to 50 wt.-% based on the whole concentrate.
[0015] The alkalinity may be achieved using any compound known in the state of the art which when dissolved in water shows an alkaline reaction, like for example alkali hydroxides, especially sodium or potassium hydroxide, ammoniumhydroxide, alkaline-earth hydrox- ides, alkali carbonates, like soda or mixtures thereof. The preferred alkalinity generating compound is represented by soda.
[0016] In a further preferred embodiment amorphous alkali silicate may be added as alkalinity source. Sodium meta silicate with a ratio of Na2O : Si02 in the range of 1 : 0,8 to 1 : 1 ,3, preferably 1 : 1 is especially appropriate.
[0017] Moreover, one or more phosphates, can be used instead of or in addition to the amorphous alkali silicate. However, this should only be in case that the use of phosphates does not cause harm because of a phosphate eliminating waste water purification step following the cleaning or washing steps.
[0018] The phosphates are preferably selected from at least one of primary ortho- phosphates represented by the general formula M'H2P04 or M"(H2P04)2 , secondary ortho- phosphates represented by the general formula M'2HP04 or MπHPO4 or tertiary orthophos- phates represented by the general formula M'3PO or M"3(P0 )2, as well as condensed phosphates derived therefrom, the so called meta phosphates and poly phosphates, with M being a metal cation , M1 preferably being an alkali metal and M" preferably being an alkaline-earth metal.
[0019] In one especially preferred embodiment the phosphate is a tripolyphosphate, preferably sodium tripolyphosphate (NasPβOio).
[0020] The content of the alkalinity source is chosen such that the pH value of a use solution containing the inventive concentrate should advantageously be in the range of from 9 to 13, preferably 10 to1 . Correspondingly, the total amount of the alkalinity source pref- erably ranges from 25 to 70 wt.-%, more preferably from 30 to 60 wt.-% and most preferred from 50 to 58 wt.-%, based on the whole concentrate.
[0021] In preferred embodiments soda is used in amounts of from 15 to 60 wt.-%, preferably 25 to 55 wt.-%. The amount of amorphous alkali silicate, especially sodium meta silicate, with the above mentioned Na20 : Si02 ratio, preferably ranges from 10 to 20 wt.-%, and especially is 15 wt.-%. The phosphor compound should be contained in an amount of at most 40 wt.-%, preferably in an amount of 30 wt.-% or below, especially in a range of from 20 to 30 wt.-% based on the whole concentrate.
[0022] It is also possible to further add an alkaline compound in form of a solid or an aqueous solution when diluting the concentrate before use. However, it is most preferred to not add further alkaline compound when preparing the use solution from the inventive concentrate.
[0023] The inventive concentrate may additionally comprise at least 1 wt.-% based on the whole concentrate of at least one alkanolamine. Preferably the sum of alkanolamines contained in the concentrate is contained in an amount above 2 wt.-% and lies within the range of from 2 to 10 wt.-%, and in particular from 3 to 5 wt.-%, based on the whole concentrate.
[0024] In a preferred embodiment at least one of the alkanolamines is represented by the general formula (III),
wherein R3 represents a hydroxyalkyl group having 1 to 6 carbon atoms, and wherein R4 and R5 independent from each other are identical with R3 or represent hydrogen. The most suitable alkanolamines are represented by mono-, di- or triethanolamine or mixtures thereof.
[0025] Those compounds may function as solutizer and thus improve the homogeneity of the inventive concentrate when diluted to form the use solution, for example the parent lye. Moreover, alkanolamines additionally represent an alkalinity source. As they are liquid they help to avoid the use of water to provide the paste-like concentrate.
[0026] The paste-like concentrate comprises a solid phase which is dispersed in a liquid phase as homogeneous as possible. The composition according to the present invention forming the above concentrate enables the water content to be reduced to an amount preferably of less than 3 wt.-%, more preferred less than 2 wt.-%, and most preferred less than 1 wt-% based on the whole concentrate. Said water content is meant to refer to free water only. Additional water may be present in form of water of crystallisation or water of constitution. To improve the physical stability as well as the chemical stability the concentrate may additionally comprise dehydration agents, for example in form of salts which bind water of crystallisation like anhydrous sodium acetate, calcium sulfate, calcium chloride, sodium hydroxide, magnesium silicate or metal oxides like CaO, MgO, P40 or Al203 or mixtures thereof.
[0027] The concentrate may additionally contain at least one alkyl polyglucoside having from 8 to 14 carbon atoms in the alkyl group and from 1 to 5 glucose moieties. The amount of the alkyl polyglucosid should be in the range of from 1 to 6 wt.%, preferably from 1,5 to 3 wt.%.
[0028] Such compounds have a strongly hydrophobic alkyl moiety and a strongly hy- drophilic glucosid moiety and, accordingly, are very much appropriate to function as stabilizer of the paste-like concentrate.
[0029] Additionally, the concentrate may comprise one or more further additives generally used in cleaning agents or detergents like further soil release agents, cobuilders, optical brighteners, dyes and fragrances, small quantities of neutral salts such as sulfates and chlorides in the form of their sodium or potassium salts, provided that these do not impair the positive properties. Other suitable additives to the product may be enzymes, foam regulators, redeposition inhibitors, soil release agents, bleaching agents from the class of per com- pounds, which are conventionally used together with activators, active chlorine compounds as well as dyes, dye transfer inhibitors or dye intensifiers and fragrances.
[0030] When preparing the inventive concentrate for practical reasons the liquid components should be pre-mixed before the solid components and further ingredients are incorporated. In case that the particulate solids are not fine enough to provide a homogeneous, paste-like concentrate, they may be grinded one or more times before incorporation.
[0031] The inventive concentrate as described above can be used to prepare a stable parent lye. Especially for usage in laundry applications the parent lye contains the inventive concentrate in amounts of from 0,5 to 25 wt.-%, preferably 5 to 15 wt.-% based on the detergent solution. Generally, the concentrate is dissolved in pure water to form the parent lye. However, it is also possible to use water in which further additives, like hydrophilic auxiliaries, are dissolved.
[0032] Although the main emphasis for the usage of the concentrate or the solution containing the inventive concentrate, respectively, is on laundry detergents, it may as well be applied as cleaning agent in warewashing, clean in place cleaners and sanitizers, food an dairy formulations and other applications in which such alkaline cleaning solutions may be applied. Preferably, the solution containing the concentrate is used as parent lye for the industrial machine cleaning of textiles.
[0033] Moreover, the present invention provides a method for washing textiles comprising one step in which a parent lye is prepared by diluting the concentrate according to claims 1 to 12 such that the parent lye contains the concentrate in an amount of from 0,5 to 25 wt.-%, preferably of from 5 to 15 wt.-% based on the detergent solution.
[0034] The concentrate according to the invention is metered from a storage reservoir using a metering equipment which is suitable to meter paste-like substances by influence of shearing force. An appropriate equipment is described for example in WO 95/09263. The required amount of the concentrate which then is free-flow is transmitted into a further tank in which it is combined and dissolved with the appropriate amount of solvent, which generally is water and may as well contain further additives or auxiliaries.
[0035] To accelerate the blending the mixture is advantageously agitated. The resulting parent lye may than either directly be distributed to the single washing machines or stored for usage in washing cycles to be performed later. Preferably, the parent lye is shortly agitated after having been stored before it is distributed to the single washing machines to guarantee a homogeneous distribution of the active agent in the parent lye. When transmitted to the single washing machines the parent lye may be further diluted depending on the desired detergent concentration.
[0036] It is also possible to pre-portion the paste-like concentrate, for example to wrap it in foil bags. Since the concentrate essentially does not contain water the concentrate may be wrapped in foils which are water soluble. In this case when preparing the parent lye the required number of foil bags is poured into a tank, the appropriate amount of water is added and after the foils are dissolved by the water the parent lye may be obtained by stirring.
[0037] A further advantage resulting from the composition of the concentrate is that it allows the purification of the waste water which is accumulated during the cleaning or wash- ing process using common membrane filtration units without blocking them or causing other damages. The membrane filtration may as well comprise at least one ultra filtration and/or reverse osmosis step. Said purification processes succeed best with a concentrate according to the invention which contains one or more phosphates.
Examples
[0038] The following table presents examples for appropriate compositions (C1 to
C10) for the inventive concentrate. The cited values refer to wt.-%, based on the whole concentrate. The paste-like concentrates exhibited good storage stabilities, i. e. they did not separate over a period of at least 12 months, provided stable parent lyes when being stirred and optionally warmed up to 30-40°C, i. e. they essentially did not separate over a period of at least 1 week, when diluted in water in an amount such that the content of the concentrate was 10 wt.-% based on the parent lye. Generally, slightly stirring was sufficient to obtain a stable parent lye. Moreover, the concentrate when used as a 10 wt.-% aqueous parent lye exhibited excellent cleaning properties. Especially when applying the concentrates in examples C3, C6, C7 and C9 the waste water accumulated during the washing process could be purified by membrane filtration even using ultra filtration steps. Table 1 : Composition of paste-like concentrates which are suitable to form stable (non separating) alkaline cleaning and detergent solutions
EO = -(OC2H4)-, PO = -(OC3H6)-

Claims

Claims
1. Paste-like, thixotropic, alkaline detergent or cleaning concentrate comprising a) at least one first component selected from one or more compounds represented by the general formula (I),
R1-(OC2H4)„-(OC3H6)m-OH (I) wherein R1 represents an unbranched or branched alkyl or alkenyl group having 4 to 8, preferably 5 to 7, carbon atoms, and wherein the sum of the average degree of ethoxylation n and propoxylation m ranges from 1 to 9, preferably from 3 to 7, with one of n and m optionally being 0, and b) at least one second component selected from one or more compounds represented by the general formula (II),
R2-(OC2H4)o-(OC3H6)p-OH (II) wherein R2 represents an unbranched or branched alkyl or alkenyl group having 9 to 22, preferably 10 to 16, carbon atoms, and wherein the sum of the average de- gree of ethoxylation o and propoxylation p ranges from 1 to 9, preferably from 3 to 7, with one of o or p optionally being 0, the cleaning concentrate exhibiting at 25°C a viscosity of from 80 000 mPas to 250 000 mPas at 5 revolutions per minute and a viscosity of from 20 000 mPas to 80 000 mPas at 50 revolutions per minute, each measured using a Brookfield rotational vis- cometer (spindle no. 7) under otherwise identical conditions.
2. Concentrate according to claim 1, characterized in that component a) is contained in an amount of from 0,5 to 15 wt.-%, preferably from 1 to 10 wt.-% based on the whole concentrate.
3. Concentrate according to claims 1 or 2, characterized in that component b) is contained in an amount of from 5 to 90 wt.-%, preferably from 15 to 70 wt.-% based on the whole concentrate.
4. Concentrate according to claims 1 to 3, characterized in that the concentrate additionally comprises at least 1 wt.-% based on the whole concentrate of at least one alka- nolamine.
5. Concentrate according to claim 4, characterized in that the sum of alkanolamines contained in the concentrate is in the range of from 2 to 10 wt.-%, preferably of from 3 to 5 wt.-% based on the whole concentrate.
6. Concentrate according to claims 4 or 5, characterized in that at least one of the alka- nolamines is represented by the general formula (III),
R \ N-RJ (III) R fit wherein R3 represents a hydroxyalkyl group having 1 to 6 carbon atoms, and wherein R4 and R5 independent from each other are identical with R3 or represent hydrogen.
7. Concentrate according to claims 4 to 6, characterized in that the concentrate comprises mono-, di- or triethanolamine or mixtures thereof.
8. Concentrate according to claims 1 to 7, characterized in that the concentrate comprises one or more phosphates.
9. Concentrate according to claim 8, characterized in that the phosphates are selected from at least one of primary orthophosphates represented by the general formula M'H2PO4 or M"(H2PO )2 , secondary orthophosphates represented by the general formula M'2HPO4 or M"HPO4 or tertiary orthophosphates represented by the general formula M' P0 or M"3(PO4)2, as well as condensed phosphates derived therefrom, the so called meta phosphates and poly phosphates, with M being a metal cation , M1 preferably being an alkali metal and M" preferably being an alkaline-earth metal.
10. Concentrate according to claims 8 or 9, characterized in that the phosphate is a tripolyphosphate, preferably sodium tripolyphosphate (Na5P30).
11. Concentrate according to claims 8 to 10, characterized in that the one or more phosphates are contained in an amount of at most 40 wt.-%, preferably in an amount of 30 wt.-% or below based on the whole concentrate.
5 12. Concentrate according to claims 1 to 11, characterized in that the concentrate additionally contains at least one alkyl polyglucosides having from 8 to 14 carbon atoms in the alkyl group and from 1 to 5 glucose moieties.
13. Concentrate according to claims 1 to 12, characterized in that the concentrate con-o tains less than 3 wt.-%, preferably less than 2 wt.-% water based on the whole concentrate.
14. Use of the concentrate according to claims 1 to 13 for the preparation of a stable parent lye.5
15. Stable parent lye containing the concentrate according to claims 1 to 12 in an amount of from 0,5 to 25 wt.-%, preferably from 5 to 15 wt.-% based on the whole parent lye.
16. Use of the parent lye according to claims 14 and 15 as a cleansing agent or a deter- o gent, preferably for the machine cleaning of textiles.
17. Method for washing textiles comprising one step in which a parent lye is prepared by diluting the concentrate according to claims 1 to 13 such that the parent lye contains the concentrate in an amount of from 0,5 to 25 wt.-%, preferably of from 5 to 15 wt.-%5 based on the parent lye.
18. Method according to claim 17, characterized in that the waste water accumulated during the whole washing process or parts thereof is purified using a membrane filtration unit.
19. Method according to claim 18, characterized in that the membrane filtration process comprises at least one ultrafiltration and/or reverse osmosis step.
EP04741679A 2004-05-28 2004-05-28 Paste-like concentrate suitable to form stable (non seperating) alkaline cleaning and detergent solutions Expired - Lifetime EP1751265B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/EP2004/050963 WO2005118767A1 (en) 2004-05-28 2004-05-28 Paste-like concentrate suitable to form stable (non seperating) alkaline cleaning and detergent solutions

Publications (2)

Publication Number Publication Date
EP1751265A1 true EP1751265A1 (en) 2007-02-14
EP1751265B1 EP1751265B1 (en) 2009-02-18

Family

ID=34957815

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04741679A Expired - Lifetime EP1751265B1 (en) 2004-05-28 2004-05-28 Paste-like concentrate suitable to form stable (non seperating) alkaline cleaning and detergent solutions

Country Status (5)

Country Link
EP (1) EP1751265B1 (en)
AT (1) ATE423188T1 (en)
DE (1) DE602004019580D1 (en)
DK (1) DK1751265T3 (en)
WO (1) WO2005118767A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8287658B2 (en) 2009-06-02 2012-10-16 Ecolab Usa Inc. Biodegradable surfactant blend

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4414708A1 (en) * 1994-04-27 1995-11-02 Henkel Ecolab Gmbh & Co Ohg Method and device for emptying a container filled with a thixotropic paste
DE19535082A1 (en) * 1995-09-21 1997-03-27 Henkel Ecolab Gmbh & Co Ohg Paste-like detergent and cleaning agent
DE19703364A1 (en) * 1997-01-30 1998-08-06 Henkel Ecolab Gmbh & Co Ohg Paste-like detergent and cleaning agent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005118767A1 *

Also Published As

Publication number Publication date
WO2005118767A1 (en) 2005-12-15
DE602004019580D1 (en) 2009-04-02
EP1751265B1 (en) 2009-02-18
DK1751265T3 (en) 2009-05-04
ATE423188T1 (en) 2009-03-15

Similar Documents

Publication Publication Date Title
EP2183346B1 (en) Paste-like detergent formulation comprising branched alkoxylated fatty alcohols as non-ionic surfactants
AU2006339687B2 (en) Liquid membrane-compatible detergent composition
EP0953631A1 (en) Stable alkaline emulsion cleaners
US8062381B2 (en) Liquid membrane compatible detergent formulation comprising branched alkoxylated fatty alcohols as non-ionic surfactants
JP4628486B2 (en) Liquid detergent composition
US5328489A (en) Non-aqueous liquid bleach containing 40-70% perborate monohydrate in a nonionic surfactant
US5364552A (en) Liquid nonionic surfactant combination having improved low-temperaturestability
IE55456B1 (en) Liquid detergent compositions
US4605506A (en) Fabric softening built detergent composition
JPH04502338A (en) Liquid or pasty bleach-containing detergents
NO314665B1 (en) Process for preparing a paste-shaped detergent and its use
JP2682534B2 (en) Paste-like low-foaming phosphorus-free detergent
US4597889A (en) Homogeneous laundry detergent slurries containing polymeric acrylic stabilizers
ZA200006602B (en) Hard surface cleaners.
US7056876B2 (en) Alkaline, hydrous paste
EP1751265B1 (en) Paste-like concentrate suitable to form stable (non seperating) alkaline cleaning and detergent solutions
EP1196535A1 (en) Liquid abrasive cleaning compositions
EP0086495A1 (en) Nonionic surfactants for automatic dishwasher detergents
JP4534193B2 (en) Powder detergent composition
EA044448B1 (en) LIQUID WASHING CONCENTRATE
JP3522589B2 (en) Method for producing surfactant composition
JPH04301000A (en) Nonionic powdery detergent composition

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: 20061017

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 IT LI LU MC NL PL PT RO SE SI SK TR

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20070713

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 IT LI LU 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: IE

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 602004019580

Country of ref document: DE

Date of ref document: 20090402

Kind code of ref document: P

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

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

Ref country code: NL

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

Effective date: 20090218

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: 20090218

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: 20090218

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: 20090529

NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

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

Effective date: 20090218

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: 20090518

Ref country code: PL

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

Effective date: 20090218

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

Ref country code: BE

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

Effective date: 20090218

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

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: 20090218

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: 20090218

Ref country code: PT

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

Effective date: 20090727

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

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: 20090218

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: 20090218

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

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

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

Ref country code: MC

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

Effective date: 20090531

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

26N No opposition filed

Effective date: 20091119

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

Effective date: 20090528

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: 20090531

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: 20090518

Ref country code: CH

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

Effective date: 20090531

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20100129

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: 20090528

Ref country code: FR

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

Effective date: 20090602

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: 20090528

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: 20090519

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: 20090528

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: 20090819

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

Ref country code: TR

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

Effective date: 20090218

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: 20090218

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602004019580

Country of ref document: DE

Representative=s name: GODEMEYER BLUM LENZE PARTNERSCHAFT, PATENTANWA, DE

Ref country code: DE

Ref legal event code: R082

Ref document number: 602004019580

Country of ref document: DE

Representative=s name: GODEMEYER BLUM LENZE PATENTANWAELTE, PARTNERSC, DE

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

Ref country code: IT

Payment date: 20230412

Year of fee payment: 20

Ref country code: DK

Payment date: 20230511

Year of fee payment: 20

Ref country code: DE

Payment date: 20230404

Year of fee payment: 20