[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

EP3666872B1 - Copolymères acryliques phosphonés pour hydrophilisation de surface - Google Patents

Copolymères acryliques phosphonés pour hydrophilisation de surface Download PDF

Info

Publication number
EP3666872B1
EP3666872B1 EP18211842.2A EP18211842A EP3666872B1 EP 3666872 B1 EP3666872 B1 EP 3666872B1 EP 18211842 A EP18211842 A EP 18211842A EP 3666872 B1 EP3666872 B1 EP 3666872B1
Authority
EP
European Patent Office
Prior art keywords
mol
monomer
acid
phosphonated
formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP18211842.2A
Other languages
German (de)
English (en)
Other versions
EP3666872A1 (fr
Inventor
Nils Wedler
Benoit Luneau
Ghislain David
Panagiotis Falireas
Claire Negrell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to EP18211842.2A priority Critical patent/EP3666872B1/fr
Publication of EP3666872A1 publication Critical patent/EP3666872A1/fr
Application granted granted Critical
Publication of EP3666872B1 publication Critical patent/EP3666872B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3784—(Co)polymerised monomers containing phosphorus
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0036—Soil deposition preventing compositions; Antiredeposition agents

Definitions

  • the present invention relates to a method of producing a phosphonated acrylic copolymer, and to the copolymer obtained by the method. Furthermore, the present invention pertains to the use of the phosphonated acrylic copolymer for hydrophilizing surfaces and to automatic dish washing and metal cleaning compositions comprising the phosphonated acrylic copolymer.
  • hydrophilization of surfaces via polymers is a common means in order to improve water spreading and thus the drain off of water from the surface, especially in cleaning applications like dishwashing or hard surface cleaning.
  • hydrophilizing surfaces less drying residues appear on reflective and transparent surfaces.
  • Such polymers often have no specific affinity to the surface and form a hydrophilic layer on the surface only via drying. Thereby, a rather high amount of polymer is needed. Furthermore, the effect is not long lasting as the polymer can be washed off.
  • Phosphonopolymers are commonly used in detergent compositions, see eg. EP0877076 A2 , DE102005059048 A1 and DE102104206148 A1 .
  • the present inventors found that the problem can be solved by a novel phosphonated acrylic copolymer. Furthermore, it has been surprisingly found that with this copolymer a thicker layer on the surface can be obtained compared to already conventionally used polymers, when applied in the same amount. Furthermore, the copolymers according to the present invention form a longer lasting layer and the drain off of water in view of the initial stainless steel surface is improved. Finally, since phosphonic groups are employed to obtain the affinity to the surface, no environmental concerns arise compared with phosphates.
  • the present invention relates in a first aspect to a method of producing a phosphonated acrylic copolymer, comprising or consisting of the steps: reacting
  • a phosphonated acrylic copolymer obtainable by the method according to the present invention is provided.
  • the invention pertains to the use of the phosphonated acrylic copolymer according to the present invention for hydrophilizing surfaces, preferably steel surfaces or silicate containing surfaces.
  • the invention refers to a dishwashing composition comprising the phosphonated acrylic copolymer of the present invention.
  • the invention pertains to a hard surface cleaning composition comprising the phosphonated acrylic copolymer of the present invention.
  • At least one relates to "at least one” and comprises 1, 2, 3, 4, 5, 6, 7, 8, 9 or more of the referenced species. Similarly, “at least one” means “one or more”, i.e. 1, 2, 3, 4, 5, 6, 7, 8, 9 or more. "At least one”, as used herein in relation to any component, refers to the number of chemically different molecules, i.e. to the number of different types of the referenced species, but not to the total number of molecules. For example, "at least one monomer of formula (I)” means that at least one type of monomer falling within the definition can be used, but that also two or more different monomers falling within this definition can be used.
  • the phosphonated acrylic copolymer in the following referred to as copolymer as well, is obtainable by a method, comprising or consisting of the steps: reacting
  • Aliphatic hydrocarbon groups preferably refer to linear or branched, substituted or unsubstituted alkyl, alkenyl, alkinly, alkylcycloalkyl, alkenylcycloalkyl, or cycloalkyl groups which can contain heteroatoms preferably selected from N, S, P, O or Si.
  • the at least one monomer of formula (I) has a number average molecular weight of 300 to 950 g/mol, preferably of 300 to 500 g/mol.
  • R 1 is methyl; and/or R 2 is an aliphatic hydrocarbon group having up to 6 carbon atoms, preferably C1 to C4 alkyl, more preferably methyl; and/or R 3 and R 4 are hydrogen or methyl; and/or X is O.
  • R 1 is methyl;
  • R 2 is an aliphatic hydrocarbon group having up to 6 carbon atoms, preferably C1 to C4 alkyl, more preferably methyl;
  • R 3 and R 4 are hydrogen or methyl; and
  • X is O.
  • R 3 and R 4 are similar.
  • the copolymer can contain further ehtylenically unsaturated monomers in up to 10 mol%. If present the at least one ethylenically unsaturated monomer is selected from C1 to C12 (meth)acrylate, acrylic acid, meth acrylic acid, vinylsulfonic acid, vinyl pyrrolidon, acrylamide, N-methyl acrylamide, maleic acid, maleic anhydride, itaconic acid, and cinnamic acid. However, in preferred embodiments only monomers according to formula (I) and formula (II) are present.
  • the at least one monomer of formula (II) is present in 0.1 to 99.9 mol%, preferably 10 to 50 mol% and/or the at least one monomer of formula (I) is present in 0.1 to 99.9 mol%, preferably 50 to 90 mol%.
  • the reaction can be performed in the presence of a radical initiator.
  • a radical initiator Any radical initiator, which is employed in the field of acrylic polymers is suitable.
  • Preferred radical initiators are selected from azobisisobutyronitrile, ammonium persulfate, hydrogen peroxide, and tert.-butyl hydroperoxide.
  • chain transfer agents e.g. mercapto acetic acid can be added in the range of 0.0025-0.25 mol% relative to the total moles of monomers of the polymerization mixture.
  • the reaction can be performed in a solvent or in a mixture of solvents. Any solvents, which are employed in the field of acrylic polymers are suitable. In preferred embodiments the reaction is performed in a solvent comprising at least one C1-C5 alcohol and/or at least one halogenated hydrocarbon solvent, like chloroform or dichloromethane and/or water.
  • the phosphonate groups can be hydrolyzed to the respective phosphonic acid groups e.g. employing equimolar amounts of trimethylsilyl bromide under anhydrous conditions.
  • the reaction can be performed at elevated temperatures of from 30 to 100°C, preferably 50 to 80°C.
  • the obtained phosphonated acrylic copolymer according to the present invention preferably has a number average molecular weight of 1,000 to 100,000 g/mol, preferably 1,500 to 10,000 g/mol.
  • Molecular weights including the number average molecular weight, are according to the invention preferably determined via GPC measurement with use of polystyrene standards, unless explicitly stated otherwise.
  • copolymers according to the present are used for hydrophilizing surfaces, preferably steel surfaces or silicate containing surfaces.
  • copolymers according to the present composition can be used in cleaning compositions.
  • the present invention refers to a dishwashing composition, preferably an automatic dishwashing composition, comprising the phosphonated acrylic copolymer of the present invention. Furthermore, the present invention refers to a hard surface, preferably metal, cleaning composition comprising the phosphonated acrylic copolymer of the present invention.
  • compositions can further contain further components commonly employed in the respective field.
  • a composition according to the invention can further comprise a bleach catalyst.
  • bleach-boosting transition metal salts or transition metal complexes such as, for example, manganese-, iron-, cobalt-, ruthenium- or molybdenum-salen or -carbonyl complexes.
  • Manganese, iron, cobalt, ruthenium, molybdenum, titanium, vanadium and copper complexes with nitrogen-containing tripod ligands, as well as cobalt-, iron-, copper- and ruthenium-ammine complexes may also be employed as the bleach catalysts.
  • Complexes of manganese in the valence state II, III, IV or V which preferably comprise one or a plurality of macrocyclic ligands with the donor functions N, NR, PR, O and/or S are particularly preferably employed.
  • Ligands having nitrogen donor functions are preferably employed.
  • bleach catalyst(s) into the compositions according to the invention, which comprise 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN), 1,4,7-triazacyclononane (TACN), 1,5, 9-trimethyl-1,5,9-triazacyclododecane (Me-TACD), 2-methyl-1,4, 7-trimethyl-1,4,7-triazacyclononane (Me/Me-TACN) and/or 2-methyl-1,4,7-triazacyclononane (Me/TACN) as the macromolecular ligands.
  • Me-TACN 1,4,7-trimethyl-1,4,7-triazacyclononane
  • TACN 1,4,7-triazacyclononane
  • Me-TACD 2-methyl-1,4, 7-trimethyl-1,4,7-triazacyclononane
  • Me/TACN 2-methyl-1,4,7-triazacyclon
  • Compositions in particular automatic dishwashing compositions, are preferred that comprise a bleach catalyst selected from the group of the bleach boosting transition metal salts and transition metal complexes, preferably from the group of the complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me/Me-TACN), as these cited bleach catalysts can particularly contribute to a significantly improved cleaning result.
  • a bleach catalyst selected from the group of the bleach boosting transition metal salts and transition metal complexes, preferably from the group of the complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me/Me-TACN), as these cited bleach catalysts can particularly contribute to a significantly improved cleaning result.
  • the above mentioned bleach boosting transition metal complexes are preferably employed in an amount of up to 5 wt.-%, particularly from 0.0025 wt.-% to 1 wt.-% and particularly preferably from 0.01 wt.-% to 0.30 wt.-%, each relative to the total weight of the compositions.
  • more bleach activator may also be employed.
  • a composition according to the invention further preferably comprises a hydrogen peroxide source.
  • the hydrogen peroxide source preferably concerns a bleaching agent, wherein oxygen bleaching agents are preferred according to present invention.
  • Sodium percarbonate, sodium perborate tetrahydrate and sodium perborate monohydrate are of particular importance among the compounds that serve as bleaching agents and liberate H 2 O 2 in water.
  • additional bleaching agents that may be used are peroxypyrophosphates, citrate perhydrates and H 2 O 2 -liberating peracidic salts or peracids, such as perbenzoates, peroxyphthalates, diperoxyazelaic acid, phthaloimino peracid or diperoxydodecanedioic acid.
  • bleaching agents from the group of the organic bleaching agents can also be employed.
  • Typical organic bleaching agents are the diacyl peroxides, such as e.g. dibenzoyl peroxide.
  • Further typical organic bleaching agents are the peroxy acids, wherein the alkylperoxy acids and the arylperoxy acids may be named as examples.
  • the hydrogen peroxide source is preferably comprised in an amount of 2-30 wt.-% and increasingly preferably in 4-25 wt.-%, in 5-20 wt.-% and particularly preferably in 6-15 wt.-% in the dishwashing composition according to the invention, each relative to the total weight of the dishwashing composition.
  • Preferred dishwashing compositions are those wherein the dishwashing composition comprises, each relative to the total weight of the dishwashing composition, 2 to 20 wt.-%, preferably 3 to 18 wt.-% and particularly 4 to 15 wt.-% of sodium percarbonate.
  • compositions according to the invention are those, wherein the bleach catalyst is selected from the group of the bleach boosting transition metal salts and transition metal complexes, preferably from the group of the complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane Me-TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me/Me-TACN), and/or the hydrogen peroxide source is sodium percarbonate, sodium perborate tetrahydrate or sodium perborate monohydrate or a combination thereof.
  • the bleach catalyst is selected from the group of the bleach boosting transition metal salts and transition metal complexes, preferably from the group of the complexes of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane Me-TACN) or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me/Me-TACN)
  • the hydrogen peroxide source is sodium percarbonate, sodium per
  • the bleach catalyst is quite particularly preferably a complex of manganese with 1,4,7-trimethyl-1,4,7-triazacyclononane (Me-TACN), in particular [Mn IV ( ⁇ -O) 3 (Me-TACN) 2 ](PF 6 ) 2 , or 1,2,4,7-tetramethyl-1,4,7-triazacyclononane (Me/Me-TACN) or a mixture therefrom, and the hydrogen peroxide source sodium percarbonate.
  • the bleach catalyst and the hydrogen peroxide source in the cited combinations are each preferably present in of the abovementioned quantities.
  • Compositions according to the invention can further comprise bleach activators, for example in order to achieve an improved bleach activity when cleaning at temperatures of 60° C and below.
  • Bleach activators which can be employed, are compounds which, under perhydrolysis conditions, yield aliphatic peroxycarboxylic acids having preferably 1 to 10 carbon atoms, in particular 2 to 4 carbon atoms, and/or optionally substituted perbenzoic acid.
  • Substances, which carry O-acyl and/or N-acyl groups of said number of carbon atoms and/or optionally substituted benzoyl groups are suitable.
  • Polyacylated alkylenediamines are preferred, tetraacetyl ethylenediamine (TAED) having proven to be particularly suitable.
  • bleach activators especially TAED, are preferably employed in amounts of 0.1-10 wt.-%, particularly 0.1-8 wt.-%, especially 2-8 wt.-% and particularly preferably 2-6 wt.-%, each relative to the total weight of the bleach activator-containing composition.
  • a dishwashing composition according to the invention concerns an automatic dishwashing composition.
  • compositions are designated as automatic dishwashing compositions, which can be employed in an automatic dishwashing process for cleaning soiled dishes.
  • the automatic dishwashing compositions according to the invention differ for example from the automatic rinsing agents that are always employed in combination with automatic dishwashing compositions and develop no inherent cleaning action.
  • compositions in particular automatic dishwashing compositions, preferably comprise builders as the essential component for the successful cleaning and rinsing. Firstly, these builders increase the alkalinity of the cleaning liquor, wherein with an increasing alkalinity fats and oils are emulsified and saponified, and secondly, reduce the water hardness of the cleaning liquor by complexing the calcium ions contained in the aqueous liquor.
  • compositions are in solid form. This is understood to mean all solid presentation forms, for example powders, granulates or extrudates.
  • a powdery composition according to the invention can exist for example as a free-flowing powder, in particular with a bulk density of 300 g/1 to 1200 g/l, especially 500 g/1 to 900 g/1 or 600 g/1 to 850 g/l.
  • compositions according to the invention are preferably in the form of a molded object, in particular a compacted material, principally a tablet.
  • a molded object in particular a compacted material, principally a tablet.
  • the molded object can also be a granulate for example that is comprised in a bag or in a cast shape.
  • compositions according to the invention can be presented as one-phase or multi-phase products.
  • Compositions in particular automatic dishwashing compositions, in particular with one, two, three or four phases, are preferred.
  • Automatic dishwashing compositions in the form of a prefabricated unit dose with two or more phases are particularly preferred.
  • tablets with two or more phases are particularly preferred, for example two-layer tablets, in particular two-layer tablets with a recess and a molded object in the recess.
  • Automatic dishwashing compositions according to the invention are preferably prefabricated as unit doses. These unit doses preferably contain the necessary quantity of washing or cleaning active substances for one cleaning cycle. Preferred unit doses weigh between 12 and 30 g, preferably between 14 and 26 g and especially between 15 and 22 g.
  • the volume of the abovementioned unit doses and their three-dimensional shape are particularly preferably chosen such that the prefabricated units can be dosed by being placed in the dosing chamber of a dishwasher. Consequently, the volume of the unit dose is preferably between 10 and 35 ml, preferably between 12 and 30 ml and especially between 15 and 25 ml.
  • the automatic dishwashing compositions according to the invention, in particular the prefabricated unit doses have, in a preferred embodiment, a water-soluble coating.
  • the manufacture of the solid compositions according to the invention presents no difficulties and can be effected by known methods, for example by spray drying or granulation, wherein enzymes and possible further heat-sensitive ingredients, such as, for example bleaching agent are optionally subsequently added separately.
  • a preferred process is one with an extrusion step.
  • the manufacture of the molded body according to the invention is preferably carried in a manner known to the person skilled in the art by compressing particulate starting materials.
  • the premix is compacted in a so-called die between two punches to form a solid core.
  • This operation which hereinafter is abbreviated to tableting, is divided into four steps: metering, compaction (elastic deformation), plastic deformation, and ejection.
  • Rotary presses are preferably used for the tableting.
  • ingredients intended for tableting can be filled simultaneously into the die in the form of a common particulate premix or filled sequentially in the form of individual, separate powders or granulates or simultaneously into the die, wherein the dosing of a prefabricated particulate premix is preferred.
  • compositions according to the invention in particular molded objects, comprise polyvinyl pyrrolidone particles.
  • These particles facilitate inter alia the disintegration of the molded objects and insofar act as disintegration auxiliaries or tablet disintegrants. It has proven to be inventively particularly advantageous to employ polyvinyl pyrrolidone particles with an average particle size of 100 to 150 ⁇ m, in particular with an average particle size of 110 to 130 ⁇ m.
  • average particle size or "average size” in the context of the present invention is understood to mean the volume average D50 particle size that can be measured using conventional methods.
  • the D50 volume average particle size is that point in the particle size distribution, at which 50 vol % of the particles have a smaller diameter and 50 vol % of the particles have a larger diameter.
  • the average particle size can be measured in particular with the help of dynamic light scattering, which is usually carried out on dilute suspensions that comprise e.g. 0.01 to 1 wt.-% of particles.
  • the PVP particles not only exhibit an average particles size of 100 to 150 ⁇ m, in particular 110 to 130 ⁇ m, but moreover that the particle size of the added particles is preferably completely within the cited ranges. This is ensured by employing particle size fractions with the cited particle sizes that were obtained by a sieving method.
  • the PVP particles are comprised in the compositions according to the invention, in particular in molded objects, preferably in an amount of 0.1 to 5 wt.-%, in particular in an amount of 0.2 to 3 wt.-%, above all in an amount of 0.3 to 1.8 wt.-%.
  • disintegrants generally consists in that their volume increases on water ingress, wherein firstly they swell, secondly the release of gas can generate a pressure that causes the tablet to disintegrate into smaller particles.
  • other disintegrants for example carbonate/citric acid systems or carbonate in combination with other organic acids, synthetic polymers or naturally occurring polymers or modified natural products such as cellulose and starch and their derivatives as well as alginates or casein derivatives can also be comprised in compositions according to the invention, in particular molded objects.
  • gas-evolving effervescent systems can also be employed as additional disintegrants.
  • Preferred effervescent systems consist of at least two ingredients that react together to form a gas, for example alkali metal carbonate and/or -hydrogen carbonate and an acidifying agent capable of releasing carbon dioxide from the alkali metal salts in aqueous solution.
  • a gas for example alkali metal carbonate and/or -hydrogen carbonate
  • an acidifying agent capable of releasing carbon dioxide from the alkali metal salts in aqueous solution.
  • One acidifying agent that releases carbon dioxide from the alkali metal salts in aqueous solution is, for example, citric acid.
  • the additional disintegration auxiliaries are preferably employed in quantities of 0.1 to 10 wt.-%, advantageously from 0.2 to 5 wt.-% and especially from 0.5 to 2 wt.-%, each relative to the total weight of the composition containing the disintegration aid.
  • compositions in particular the dishwashing compositions are in the form of a liquid, gel or paste.
  • liquid or free-flowing dosage forms can be used as the liquid composition.
  • free-flowing is understood to mean preparations that are pourable and can have viscosities up to several 10 000 mPas.
  • the viscosity can be measured using standard methods (for example using a Brookfield-Viscosimeter LVT-II at 20 rpm and 20° C, spindle 3) and is preferably in the range of 5 to 10 000 mPas.
  • Preferred compositions have viscosities from 10 to 8000 mPas, particularly preferably from 120 to 3000 mPas.
  • a liquid composition can therefore also be in gel form or in paste form, it can be a homogenous solution or suspension, it can be sprayable for example or can be packaged in other usual dosage forms.
  • Liquid or pasty inventive compositions in the form of solutions in standard solvents are generally prepared by a simple mixing of the ingredients, which can be added as is or as a solution into an automatic mixer.
  • embodiments of the present invention further include all solid, powdery, liquid, gellified or pasty presentation forms of the compositions which can also optionally consist of a plurality of phases as well as being in a compressed on non-compressed form.
  • a composition according to the invention can also be packaged in a container, preferably an air-permeable container, from which the composition is released shortly before use or during the cleaning procedure.
  • a composition in particular a dishwashing composition, according to the invention additionally comprises another ingredient that is selected from the group consisting of builder, surfactant, anionic polymer as well as combinations hereof.
  • a dishwashing composition according to the invention is essentially phosphate-free, i.e. contains less than 0.05 wt.-% phosphate compounds or is free from phosphate compounds. Phosphate-free dishwashing compositions according to the invention are particularly advantageous with respect to environmental considerations.
  • the group of preferred builders includes in particular the citrates as well as the carbonates and the organic co-builders.
  • the term "citrate” hereby includes both citric acid as well as its salts, in particular its alkali metal salts.
  • Particularly preferred dishwashing compositions according to the invention in particular automatic dishwashing compositions, comprise citric acid and citrate, preferably sodium citrate, in amounts of 5 to 60 wt.-%, preferably 10 to 50 wt.-% and particularly 15 to 40 wt.-%.
  • Carbonate(s) and/or hydrogen carbonate(s), preferably alkali metal carbonate(s), particularly preferably sodium carbonate, are particularly preferably added in quantities of 5 to 50 wt.-%, preferably 10 to 40 wt.-% and especially 15 to 30 wt.-%, each relative to the weight of the composition.
  • Polycarboxylates/polycarboxylic acids and phosphonates may be particularly mentioned as the organic co-builders. These classes of substances are described below.
  • Useful organic builders are, for example, the polycarboxylic acids that can be used in the form of the free acid and/or their sodium salts, polycarboxylic acids in this context being understood to be carboxylic acids that carry more than one acid function. These include, for example, adipic acid, succinic acid, glutaric acid, malic acid, tartaric acid, maleic acid, fumaric acid, sugar acids, amino carboxylic acids, nitrilotriacetic acid (NTA) and mixtures thereof. Besides their building effect, the free acids also typically have the property of an acidifying component and hence also serve to establish a relatively low and mild pH of the inventive compositions. Succinic acid, glutaric acid, adipic acid, gluconic acid and any mixtures thereof are particularly to be mentioned in this regard.
  • the phosphonate complexants include a series of different compounds such as for example diethylenetriamine penta(methylene phosphonic acid) (DTPMP). Hydroxyalkane phosphonates or amino alkane phosphonates are particularly preferred according to the invention.
  • HEDP 1-hydroxyethane-1,1-diphosphonate
  • It is normally added as the sodium salt, the disodium salt reacting neutral and the tetrasodium salt reacting alkaline (pH 9).
  • Ethylenediamine tetramethylene phosphonate (EDTMP), diethylenetriamine pentamethylene phosphonate (DTPMP) and their higher homologs are preferably chosen as the aminoalkane phosphonates. They are preferably added in the form of the neutral-reacting sodium salts, e.g. as the hexasodium salt of EDTMP or as the hepta- and octasodium salt of DTPMP. Of the class of phosphonates, HEDP is preferably used as the builder.
  • the aminoalkane phosphonates additionally possess a pronounced ability to complex heavy metals. Accordingly, it can be preferred, particularly where the compositions also contain bleach, to use amino alkane phosphonates, particularly DTPMP, or mixtures of the cited phosphonates.
  • a preferred composition preferably a dishwashing composition, in particular an automatic dishwashing composition, comprises one or more phosphonate(s) from the group
  • compositions in particular automatic dishwashing compositions, comprise 1-hydroxyethane-1,1-diphosphonic acid (HEDP) or diethylenetriamine penta(methylene phosphonic acid) (DTMP) as the phosphonates.
  • HEDP 1-hydroxyethane-1,1-diphosphonic acid
  • DTMP diethylenetriamine penta(methylene phosphonic acid)
  • the weight fraction of the phosphonates in the total weight of the compositions according to the invention, in particular the automatic dishwashing composition is advantageously 1 to 8 wt.-%, preferably 1.2 to 6 wt.-% and especially 1.5 to 4 wt.-%.
  • compositions according to the invention in particular the automatic dishwashing compositions, can comprise one or more surfactants, wherein anionic surfactants, non-ionic surfactants and their mixtures particularly come into question.
  • anionic surfactants possess at least one sulfate or sulfonate group.
  • the anionic surfactant with at least one sulfate or sulfonate group is preferably selected from fatty alcohol sulfates, alkane sulfonates and alkylbenzene sulfonates.
  • C12-C18 fatty alcohol sulfates e.g. Sulfopon K 35 (Cognis, Germany)
  • SAS secondary C13-C17 alkane sulfonates
  • SAS Hostapur SAS 93
  • linear C8-C18 alkylbenzene sulfonates in particular dodecylbenzene sulfonate (LAS) are particularly preferred in this regard.
  • the terms “sulfate” and “sulfonate” also include, in addition to the anionic compounds in question that are present in the form of salts, the free acids, i.e. the corresponding alkyl sulfur acids or alkyl sulfonic acids.
  • the anionic surfactant containing at least one sulfate or sulfonate group is preferably comprised in compositions according to the invention in an amount of 0.1 to 20 wt.-%, particularly preferably 0.5 to 15 wt.-%, in particular 2.5 to 10 wt.-%.
  • non-ionic surfactants known to the person skilled in the art can be used as the non-ionic surfactants.
  • Suitable exemplary non-ionic surfactants are alkyl glycosides that satisfy the general Formula RO(G)x, in which R means a primary linear or methyl-branched, particularly 2-methyl-branched, aliphatic group containing 8 to 22 and preferably 12 to 18 carbon atoms and G stands for a glycose unit containing 5 or 6 carbon atoms, preferably glucose.
  • the degree of oligomerization x which defines the distribution of monoglycosides and oligoglycosides, is any number between 1 and 10, preferably x is 1.2 to 1.4.
  • non-ionic surfactants which may be used, either as the sole non-ionic surfactant or in combination with other non-ionic surfactants, are alkoxylated, preferably ethoxylated or ethoxylated and propoxylated fatty acid alkyl esters preferably containing 1 to 4 carbon atoms in the alkyl chain.
  • Non-ionic surfactants of the amine oxide type for example N-cocoalkyl-N,N-dimethylamine oxide and N-tallow alkyl-N,N-dihydroxyethylamine oxide, and the fatty acid alkanolamides may also be suitable.
  • the quantity in which these non-ionic surfactants are used is preferably no more than the quantity in which the ethoxylated fatty alcohols are used and, particularly no more than half that quantity.
  • Suitable surfactants are polyhydroxyfatty acid amides corresponding to following formula in which R stands for an aliphatic acyl residue with 6 to 22 carbon atoms, R 1 for hydrogen, an alkyl or hydroxyalkyl residue with 1 to 4 carbon atoms and [Z] for a linear or branched polyhydroxyalkyl residue with 3 to 10 carbon atoms and 3 to 10 hydroxyl groups.
  • the polyhydroxyfatty acid amides are known substances, which may normally be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride.
  • the group of the polyhydroxyfatty acid amides also includes compounds corresponding to the following formula in which R is a linear or branched alkyl or alkenyl group containing 7 to 12 carbon atoms, R 1 is a linear, branched or cyclic alkyl residue or an aryl residue containing 2 to 8 carbon atoms and R 2 is a linear, branched or cyclic alkyl residue or an aryl residue or an oxyalkyl residue containing 1 to 8 carbon atoms, C1-4 alkyl- or phenyl residues being preferred, and [Z] is a linear polyhydroxyalkyl residue, of which the alkyl chain is substituted by at least two hydroxy groups, or alkoxylated, preferably ethoxylated or propoxylated derivatives of that group.
  • [Z] is preferably obtained by reductive amination of a reducing sugar, for example glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • a reducing sugar for example glucose, fructose, maltose, lactose, galactose, mannose or xylose.
  • the N-alkoxy- or N-aryloxy-substituted compounds may then be converted into the required polyhydroxyfatty acid amides by reaction with fatty acid methyl esters in the presence of an alkoxide as the catalyst.
  • the preferred surfactants are weakly foaming non-ionic surfactants.
  • Compositions, particularly cleaning compositions for dishwashing and among this preferably for automatic dishwashers, are especially preferred when they comprise non-ionic surfactants from the group of the alkoxylated alcohols.
  • Preferred non-ionic surfactants are alkoxylated, advantageously ethoxylated, particularly primary alcohols preferably containing 8 to 18 carbon atoms and, on average, 1 to 12 moles of ethylene oxide (EO) per mole of alcohol, in which the alcohol group may be linear or, preferably, methyl-branched in the 2-position or may contain e.g. linear and methyl-branched residues in the form of the mixtures typically present in Oxo alcohol residues.
  • EO ethylene oxide
  • alcohol ethoxylates with linear groups from alcohols of natural origin with 12 to 18 carbon atoms e.g. from coco-, palm-, tallow- or oleyl alcohol, and an average of 2 to 8 EO per mole alcohol.
  • exemplary preferred ethoxylated alcohols include C12-14 alcohols with 3 EO or 4 EO, C9-11 alcohols with 7 EO, C13-15 alcohols with 3 EO, 5 EO or 7 EO, C12-18 alcohols with 3 EO, 5 EO or 7 EO and mixtures thereof, such as mixtures of C12-14 alcohols with 3 EO and C12-18 alcohols with 5 EO.
  • the cited degrees of ethoxylation constitute statistically average values that can be a whole or a fractional number for a specific product.
  • Preferred alcohol ethoxylates have a narrowed homolog distribution (narrow range ethoxylates, NRE).
  • fatty alcohols with more than 12 EO can also be used. Examples of these are tallow fatty alcohol with 14 EO, 25 EO, 30 EO or 40 EO.
  • ethoxylated non-ionic surfactant(s) prepared from C6-20 monohydroxy alkanols or C6-20 alkylphenols or C12-20 fatty alcohols and more than 12 mole, preferably more than 12 mole and especially more than 20 mole ethylene oxide per mole alcohol, are used with particular preference.
  • a particularly preferred non-ionic surfactant is obtained from a straight-chain fatty alcohol containing 16 to 20 carbon atoms (C16-20 alcohol), preferably a C18 alcohol, and at least 12 moles, preferably at least 15 moles and more preferably at least 20 moles of ethylene oxide.
  • the so-called narrow range ethoxylates are particularly preferred.
  • surfactant(s) that comprise one or more tallow fat alcohols with 20 to 30 EO in combination with a silicone defoamer are particularly preferably used.
  • Non-ionic surfactants that have a melting point above room temperature are used with particular preference.
  • Suitable non-ionic surfactants with a melting and/or softening point in the cited temperature range are, for example weakly foaming non-ionic surfactants that can be solid or highly viscous at room temperature. If non-ionic surfactants are used that are highly viscous at room temperature, then it is preferred that they have a viscosity greater than 20 Pas, preferably above 35 Pas and especially above 40 Pas. Non-ionic surfactants that have a waxy consistency at room temperature are also preferred.
  • Non-ionic surfactants from the group of the alkoxylated alcohols particularly preferably from the group of the mixed alkoxylated alcohols and especially from the group of the EO-AO-EO-non-ionic surfactants are likewise incorporated with particular preference.
  • the room temperature solid non-ionic surfactant additionally has propylene oxide units in the molecule.
  • These PO units preferably make up as much as 25% by weight, more preferably as much as 20% by weight and, especially up to 15% by weight of the total molecular weight of the non-ionic surfactant.
  • Particularly preferred non-ionic surfactants are ethoxylated monohydroxyalkanols or alkylphenols, which have additional polyoxyethylene-polyoxypropylene block copolymer units.
  • the alcohol or alkylphenol component of these non-ionic surfactant molecules preferably makes up more than 30 wt.-%, more preferably more than 50 wt.-% and most preferably more than 70 wt.-% of the total molecular weight of these non-ionic surfactants.
  • Preferred compositions are characterized in that they comprise ethoxylated and propoxylated non-ionic surfactants, in which the propylene oxide units in the molecule preferably make up as much as 25% by weight, more preferably as much as 20% by weight and, especially up to 15% by weight of the total molecular weight of the non-ionic surfactant.
  • Preferred surfactants that are solid at room temperature are used and belong to the groups of the alkoxylated non-ionic surfactants, more particularly the ethoxylated primary alcohols, and mixtures of these surfactants with structurally more complex surfactants, such as polyoxypropylene/polyoxyethylene/polyoxypropylene ((PO/EO/PO) surfactants).
  • Such (PO/EO/PO) non-ionic surfactants are moreover characterized as having good foam control.
  • non-ionic surfactants with melting points above room temperature comprise 40 to 70% of a polyoxypropylene/polyoxyethylene/polyoxypropylene block polymer blend, which comprises 75% by weight of an inverted block copolymer of polyoxyethylene and polyoxypropylene with 17 moles of ethylene oxide and 44 moles of propylene oxide and 25% by weight of a block copolymer of polyoxyethylene and polyoxypropylene initiated with trimethylol propane and comprising 24 moles of ethylene oxide and 99 moles of propylene oxide per mole of trimethylol propane.
  • non-ionic surfactants in the context of the present invention have proved to be weakly foaming non-ionic surfactants, which have alternating ethylene oxide and alkylene oxide units.
  • the surfactants with EO-AO-EO-AO blocks are again preferred, wherein one to ten EO or AO groups respectively are linked together, before a block of the other groups follows.
  • non-ionic surfactants of the general formula are preferred, in which R 1 stands for a linear or branched, saturated or a mono or polyunsaturated C 6 - 24 alkyl or -alkenyl group, each group R 2 or R 3 independently of one another is selected from -CH 3 , -CH 2 CH 3 , -CH 2 CH 2 -CH 3 , CH(CH 3 ) 2 , and the indices w, x, y, z independently of one another stand for whole numbers from 1 to 6.
  • the preferred non-ionic surfactants of the previous formula can be manufactured by known methods from the corresponding alcohols R1-OH and ethylene oxide or alkylene oxide.
  • the group R1 in the previous Formula can vary depending on the origin of the alcohol. When natural sources are used, the group R1 has an even number of carbon atoms and generally is not branched, the linear alcohols of natural origin with 12 to 18 carbon atoms, for example coconut, palm, tallow or oleyl alcohol being preferred.
  • the alcohols available from synthetic sources are, for example Guerbet alcohols or mixtures of methyl branched in the 2-position or linear and methyl branched groups, as are typically present in Oxo alcohols.
  • non-ionic surfactants are preferred, in which R1 in the previous formula stands for an alkyl group containing 6 to 24, preferably 8 to 20, particularly preferably 9 to 15 and particularly 9 to 11 carbon atoms.
  • butylene oxide can be the alkylene oxide unit that alternates with the ethylene oxide unit in the preferred non-ionic surfactants.
  • R 2 or R 3 independently of one another are selected from - CH 2 CH 2 -CH 3 or CH(CH 3 ) 2 .
  • non-ionic surfactants of the previous formula are used, in which R 2 or R 3 stand for a group -CH 3 , w and x independently of one another stand for values of 3 or 4 and y and z independently of one another stand for values of 1 or 2.
  • non-ionic surfactants are preferred that have a C9-15 alkyl group with 1 to 4 ethylene oxide units, followed by 1 to 4 propylene oxide units, followed by 1 to 4 ethylene oxide units, followed by 1 to 4 propylene oxide units.
  • These surfactants exhibit the required low viscosity in aqueous solution and according to the invention are used with particular preference.
  • Particularly preferred non-ionic surfactants are of the general formula R1-O[CH 2 CH(CH 3 )O] x [CH 2 CH 2 O] y [CH 2 CH(CH 3 )O] z CH 2 CH(OH)R2, in which R1 stands for a linear or branched aliphatic hydrocarbon residue with 4 to 22 carbon atoms, particularly 6 to 18 carbon atoms, or mixtures thereof, R2 means a linear or branched hydrocarbon residue with 2 to 26 carbon atoms or mixtures thereof and x and z stand for values between 0 and 40 and y stands for a value of at least 15, preferably 15 to 120, particularly preferably from 20 to 80.
  • compositions in particular the automatic dishwashing compositions, comprise, relative to its total weight, non-ionic surfactant of the general formula R1-O[CH 2 CH(CH 3 )O] x [CH 2 CH 2 O] y [CH 2 CH(CH 3 )O] z CH 2 CH(OH)R2 in amounts of 0.1 to 15 wt . -%, preferably 0.2 to 10 wt.-%, particularly preferably 0.5 to 8 wt.-% and in particular from 1.0 to 6 wt.-%.
  • non-ionic surfactant of the general formula R1-O[CH 2 CH(CH 3 )O] x [CH 2 CH 2 O] y [CH 2 CH(CH 3 )O] z CH 2 CH(OH)R2 in amounts of 0.1 to 15 wt . -%, preferably 0.2 to 10 wt.-%, particularly preferably 0.5 to 8 wt.-% and in particular from 1.0 to 6 wt.-%.
  • R1-O[CH 2 CH 2 O] y CH 2 CH(OH)R2 are particularly preferred, in which R1 stands for a linear or branched aliphatic hydrocarbon residue with 4 to 22 carbon atoms, particularly 6 to 18 carbon atoms, or mixtures thereof, R2 means a linear or branched hydrocarbon residue with 2 to 26, especially 4 to 20 carbon atoms or mixtures thereof and y stands for a value between 15 and 120, preferably 20 to 100, in particular 20 to 80.
  • the group of these non-ionic surfactants includes for example hydroxy mixed ethers of the general formula C 6-22 CH(OH)CH 2 O-(EO) 20-120 -C 2-26 , for example the C 8-12 fatty alcohol-(EO) 22 -2-hydroxydecyl ethers and the C 4-22 fatty alcohol-(EO) 40-80 -2-hydroxyalkyl ethers.
  • a composition according to the invention in particular an automatic dishwashing composition, wherein a surfactant is employed as the weakly foaming non-ionic surfactant of the general Formula R1CH(OH)CH 2 O-(CH 2 CH 2 O) 20-120 -R2, wherein R1 and R2 independently of one another stand for a linear or branched aliphatic hydrocarbon residue with 2 to 20, particularly 4 to 16 carbon atoms, are particularly preferred.
  • a surfactant is employed as the weakly foaming non-ionic surfactant of the general Formula R1CH(OH)CH 2 O-(CH 2 CH 2 O) 20-120 -R2, wherein R1 and R2 independently of one another stand for a linear or branched aliphatic hydrocarbon residue with 2 to 20, particularly 4 to 16 carbon atoms, are particularly preferred.
  • surfactants of the formula R1-O[CH 2 CH(CH 3 )O] x [CH 2 CH 2 O] y CH 2 CH(OH)R2, in which R1 stands for a linear or branched aliphatic hydrocarbon residue with 4 to 22 carbon atoms or mixtures thereof, R2 means a linear or branched hydrocarbon residue with 2 to 26 carbon atoms or mixtures thereof and x stands for values between 0.5 and 4, preferably 0.5 to 1.5, and y stands for a value of at least 15.
  • surfactants are also of the general formula R1-O[CH 2 CH(CH 3 )O] x [CH 2 CH 2 O] y [CH 2 CH(OH)R2, in which R1 stands for a linear or branched aliphatic hydrocarbon group with 4 to 22 carbon atoms or mixtures thereof, R2 means a linear or branched hydrocarbon group with 2 to 26 carbon atoms or mixtures thereof and x stands for values between 1 and 40 and y stands for a value between 15 and 40, wherein the alkylene units [CH 2 CH(CH 3 )O] and [CH 2 CH 2 O] are randomized, i.e. exist in the form of a statistical, random distribution.
  • non-ionic surfactants are the end-capped poly(oxyalkylated) non-ionic surfactants corresponding to the formula R1-O[CH 2 CH(R3)O] x [CH 2 ] k CH(OH)[CH 2 ] j OR2, in which R1 and R2 stand for linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon groups containing 1 to 30 carbon atoms, R3 stands for H or for a methyl, ethyl, n-propyl, isopropyl, n-butyl, 2-butyl or 2-methyl-2-butyl group, x for values between 1 and 30, k and j have values between 1 and 12, preferably between 1 and 5.
  • R1-O[CH 2 CH(R3)O] x [CH 2 ] k CH(OH)[CH 2 ] j OR2 can be different for the case where x ⁇ 2.
  • R1 and R2 are preferably linear or branched, saturated or unsaturated, aliphatic or aromatic hydrocarbon groups containing 6 to 22 carbon atoms, groups containing 8 to 18 carbon atoms being particularly preferred.
  • H, -CH 3 or -CH 2 CH 3 are particularly preferred for the group R3.
  • Particularly preferred values for x are in the range from 1 to 20 and more particularly in the range from 6 to 15.
  • each R3 in the above formula can be different for the case where x ⁇ 2.
  • the alkylene oxide unit in the straight brackets can be varied.
  • the value 3 for x was selected by way of example and may easily be larger, the range of variation increasing with increasing x-values and including, for example, a large number of (EO) groups combined with a small number of (PO) groups or vice versa.
  • Particularly preferred end-capped poly(oxyalkylated) alcohols corresponding to the above formula have values for both k and j of 1, so that the above formula can be simplified to R1-O[CH 2 CH(R3)O] x CH 2 CH(OH)CH 2 OR2
  • R1, R2 and R3 are as defined above and x stands for numbers from 1 to 30, preferably 1 to 20 and especially 6 to 18.
  • non-ionic surfactants are non-ionic surfactants of the general formula R1-O(AlkO)xM(OAlk)yOR2, wherein R1 and R2 independently of one another stand for a branched or unbranched, saturated or unsaturated, optionally hydroxylated group with 4 to 22 carbon atoms; Alk stands for a branched or unbranched alkyl group with 2 to 4 carbon atoms; x and y independently of one another stand for values between 1 and 70; and M stands for an alkyl group from the group CH 2 , CHR3, CR3R4, CH 2 CHR3 and CHR3CHR4, wherein R3 and R4 independently of one another stand for branched or unbranched, saturated or unsaturated alkyl groups with 1 to 18 carbon atoms.
  • non-ionic surfactants are preferred with the general formula R1-CH(OH)CH 2 -O(CH 2 CH 2 O) x CH 2 CHR(OCH 2 CH 2 ) y O-CH 2 CH(OH)-R2, wherein R, R1 and R2 independently of each other stand for an alkyl group or alkenyl group containing 6 to 22 carbon atoms; x and y independently of one another stand for values between 1 and 40.
  • R1-CH(OH)CH 2 -O(CH 2 CH 2 O) x CH 2 CHR(OCH 2 CH 2 )yO-CH 2 CH(OH)-R2 in which R stands for a linear, saturated alkyl group with 8 to 16 carbon atoms, preferably 10 to 14 carbon atoms and n and m independently of one another have values of 20 to 30.
  • Appropriate compounds can be obtained for example by treating alkyl diols HO-CHR-CH2-OH with ethylene oxide, wherein subsequently the free OH functionalities are treated with an alkyl epoxide to afford a dihydroxy ether.
  • the non-ionic surfactant is selected from non-ionic surfactants of the general formula R1-O(CH 2 CH 2 O)xCR3R4(OCH 2 CH 2 ) y O-R2, in which R1 and R2 independently of one another stand for an alkyl group or alkenyl group containing 4 to 22 carbon atoms; R3 and R4 independently of one another stand for H or an alkyl group or alkenyl group containing 1 to 18 carbon atoms and x and y independently of one another stand for values between 1 and 40.
  • R1 and R2 independently of one another stand for an alkyl group or alkenyl group containing 4 to 22 carbon atoms
  • R3 and R4 independently of one another stand for H or an alkyl group or alkenyl group containing 1 to 18 carbon atoms
  • x and y independently of one another stand for values between 1 and 40.
  • R1-O(CH 2 CH 2 O)xCR3R4(OCH 2 CH 2 ) y O-R2 in which R3 and R4 stand for H and the indices x and y independently of one another assume values of 1 to 40, preferably from 1 to 15.
  • particularly preferred compounds are of the general formula R1-O(CH 2 CH 2 O) x CR3R4(OCH 2 CH 2 ) y O-R2, in which the R1 and R2 groups independently of one another represent saturated alkyl groups with 4 to 14 carbon atoms and the indices x and y independently of one another assume values of 1 to 15 and especially 1 to 12.
  • Quite particularly preferred compounds are of the general formula R1-O(CH 2 CH 2 O) x CR3R4(OCH 2 CH 2 ) y O-R2, in which the indices x and y independently of one another assume values from 8 to 12.
  • the cited carbon chain lengths and degrees of ethoxylation or alkoxylation of the abovementioned non-ionic surfactants constitute statistically average values that can be a whole or a fractional number for a specific product. Due to the manufacturing processes, commercial products of the cited formulas do not consist in the main of one sole representative, but rather are a mixture, wherein not only the carbon chain lengths but also the degrees of ethoxylation or alkoxylation can be average values and thus be fractional numbers.
  • Non-ionic surfactants that have a melting point above room temperature are particularly preferred.
  • the weight fraction of the non-ionic surfactant in the total weight of the composition according to the invention, particularly an automatic dishwashing composition is 0.1 to 20 wt.-%, particularly preferably 0.5 to 15 wt.-%, in particular 2.5 to 10 wt.-%.
  • the wt.-% ratio of the anionic surfactant with at least one sulfate or sulfonate group to the non-ionic surfactant is from 3:1 to 1:3, especially 2:1 to 1:2, particularly preferably 1.5:1 to 1:1.5.
  • a composition according to the invention further comprises at least one enzyme, in particular a protease, amylase, cellulase, pectin-cleaving enzyme, hemicellulase, mannanase, tannase, xylanase, xanthanase, ⁇ -gtucosidase, carrageenase, perhydrolase, oxidase, oxidoreductase or a lipase, as well as combinations hereof, in particular a combination that is selected from protease and amylase, protease and lipase, protease and cellulase, protease and mannanase, amylase and lipase, amylase and cellulase, amylase and mannanase, lipase and cellulase, lipase and mannanase, lipase and cellulase and cellulase
  • Enzymes of this type are each preferably comprised in the composition in a total amount of 1 ⁇ 10 -8 to 5 wt.-% based on the active protein.
  • Each additional enzyme is comprised with increasing preference in compositions according to the invention in an amount of 1 ⁇ 10 -7 to 3 wt.-%, 0.00001 to 1 wt.-%, 0.00005 to 0.5 wt.-%, 0.0001 to 0.1 wt.-% and particularly preferably 0.0001 to 0.05 wt.-%, based on active protein.
  • the active protein concentration can be determined in a customary manner for hydrolases for example by titrating the active centers in the presence of a suitable irreversible inhibitor and measuring the residual activity (see for example M.
  • the enzymes particularly preferably exhibit synergistic cleaning powers towards certain soils or stains, i.e. the enzymes comprised in the composition mutually support each other in their cleaning power.
  • Synergistic effects can not only appear between various enzymes but also between one or more enzymes and additional ingredients of the composition according to the invention.
  • Preferred proteases are those of the subtilisin type. Examples of these are subtilisins BPN' and Carlsberg, the protease PB92, the subtilisins 147 and 309, the alkaline protease from Bacillus lentus, subtilisin DY and those enzymes of the subtilases no longer however classified in the stricter sense as subtilisins thermitase, proteinase K and the proteases TW3 and TW7.
  • Subtilisin Carlsberg in further developed form is available under the trade name Alcalase® from Novozymes A/S, Bagsv ⁇ rd, Denmark.
  • subtilisins 147 and 309 are commercialized under the trade names Esperase® and Savinase® by the Novozymes company.
  • the protease variants sold under the name BLAP® are derived from the protease from Bacillus lentus DSM 5483. Additional preferred proteases are furthermore for example the enzymes sold under the name PUR.
  • proteases are furthermore the enzymes available with the trade names Durazym®, Relase®, Everlase®, Nafizym®, Natalase®, Kannase® and Ovozyme® from the Novozymes Company, those under the trade names Purafect®, Purafect® OxP, Purafect® Prime, Excellase® and Properase® from Genencor, that under the trade name Protosol® from Advanced Biochemicals Ltd., Thane, India, that under the trade name Wuxi® from Wuxi Snyder Bioproducts Ltd., China, those under the trade names Proleather® and Protease P® from Amano Pharmaceuticals Ltd., Nagoya, Japan, and that under the designation Proteinase K-16 from Kao Corp., Tokyo, Japan.
  • the proteases from Bacillus gibsonii and Bacillus pumilus which are disclosed in the international patent applications WO2008/086916 and WO2007/131656 are particularly preferably employed.
  • conditionable amylases are the ⁇ -amylases from Bacillus licheniformis, from Bacillus amyloliquefaciens or from Bacillus stearothermophilus, as well as in particular their improved further developments for use in washing or cleaning compositions.
  • the enzyme from Bacillus licheniformis is available from the Novozymes Company under the name Termamyl® and from the Danisco/Genencor Company under the name Purastar®ST.
  • ⁇ -amylase Further development products of this ⁇ -amylase are available from the Novozymes Company under the trade names Duramyl® and Termamyl® ultra, from the Danisco/Genencor Company under the name Purastar® OxAm and from Daiwa Seiko Inc., Tokyo, Japan as Keistase®.
  • the ⁇ -amylase from Bacillus amyloliquefaciens is commercialised by the Novozymes Company under the name BAN®, and derived variants from the ⁇ -amylase from Bacillus stearothermophilus under the names BSG® and Novamyl® also from the Novozymes Company.
  • a 7-7 (DSM 12368) and the cyclodextrin-glucanotransferase (CGTase) from Bacillus agaradherens (DSM 9948). Fusion products of all the cited molecules can also be employed. Moreover, further developments of ⁇ -amylase from Aspergillus niger and A. oryzae available from the Company Novozymes under the trade name Fungamyl® are suitable. Additional commercial products that can be advantageously used are for example the Amylase-LT® and Stainzyme® or Stainzyme ultra® or Stainzyme plus®, the last also from the Novozymes company. Variants of these enzymes obtained by point mutations can also be inventively employed.
  • amylases are disclosed in the international applications WO 00/60060 , WO 03/002711 , WO 03/054177 and WO 07/079938 , to which disclosures reference is therefore expressly made or in this regard their disclosed content is therefore expressly incorporated into the present patent application.
  • Inventively conditionable amylases are moreover preferably ⁇ -amylases.
  • Exemplary inventively conditionable lipases or cutinases that are comprised in particular due to their triglyceride-cleaving activities, but also to generate peracids in situ from appropriate precursors, are the lipases that are originally obtainable from Humicola lanuginose (Thermomyces lanuginosus) or further developed lipases, especially those with the amino acid exchange D96L. They are commercialized, for example by the Novozymes Company under the trade names Lipolase®, Lipolase® Ultra, LipoPrime®, Lipozyme® and Lipex®.
  • suitable cutinases for example are those that were originally isolated from Fusarium solani pisi and Humicola insolens.
  • Suitable lipases or cutinases whose starting enzymes were originally isolated from Pseudomonas mendocina and Fusarium solanii are for example available from Genencor Company.
  • Further important commercial products that may be mentioned are the commercial preparations M1 Lipase® and Lipomax® originally from Gist-Brocades Company, and the commercial enzymes from the Meito Sangyo KK Company, Japan under the names Lipase MY-30®, Lipase OF® and Lipase PL® as well as the product Lumafast® from the Genencor Company.
  • Inventively conditionable cellulases include for example the fungal, endoglucanase (EG)-rich cellulase preparation or its further developments that are offered by the Novozymes Company under the trade name Celluzyme®.
  • the products Endolase® and Carezyme® based on the 50 kD-EG, respectively 43 kD-EG from Humicola insolens DSM 1800 are also obtainable from the Novozymes Company.
  • Additional employable commercial products from this company are Cellusoft®, Renozyme® and Celluclean®.
  • Cellulases for example, which are available under the trade names Ecostone® and Biotouch® from AB Enzymes, Finland can also be used and which are at least partially based on the 20 kD-EG from Melanocarpus. Additional cellulases from the AB Enzymes Company are Econase® and Ecopulp®. Further suitable cellulases are from Bacillus sp. CBS 670.93 and CBS 669.93, the CBS 670.93 from Bacillus sp. being available under the trade name Puradax® from the Danisco/Genencor Company. Additional useable commercial products of the Danisco/Genencor Company are "Genencor detergent cellulase L" and IndiAge®Neutra.
  • variants of these enzymes obtained by point mutations can also be inventively employed.
  • Particularly preferred cellulases are Thielavia terrestris cellulase variants, which are disclosed in the international application WO 98/12307 , cellulases from Melanocarpus, in particular Melanocarpus albomyces, which are disclosed in the international application WO 97/14804 , cellulases of the EGIII type from Trichoderma reesei, which are disclosed in the European patent application EP 1 305 432 or variants that can be obtained from them, in particular those that are disclosed in the European patent applications EP 1240525 and EP 1305432 , as well as cellulases, which are disclosed in the international patent applications WO 1992006165 , WO 96/29397 and WO 02/099091 . Reference is therefore expressly made to their respective disclosure or their disclosed content in this regard is therefore expressly incorporated into the present patent application.
  • pectin-cleaving enzymes are enzymes that cleave pectin and/or other galacturonanes.
  • Pections are polysaccharides, whose major constituent is ⁇ -D-galacturonic acid as the monomer, preferably to at least 50 wt.-% and particularly preferably to at least 65 wt.-%.
  • These galacturonic acid monomers are linked together though ⁇ -1,4-, sometimes also with a minor fraction through ⁇ -1,4-glycosidic bonds, and form the backbone of the pectin molecule that is periodically interrupted by 1,2-bonds with ⁇ -L-rhamnose.
  • pectin is a rhamno-galacturonic acid. Consequently, a pectin-cleaving enzyme is in particular an enzyme that catalyzes the hydrolysis of 1,4- ⁇ -D-galactosiduronic bonds.
  • the pectin-cleaving enzymes particularly belong to the enzyme classes (Enzyme Commission number) EC 3.1.1.1 1, EC 3.2.1.15, EC 3.2.1.67 and EC 3.2.1.82, and consequently fall into the third of the six major classes of enzymes, the hydrolases (E.C.3.-.-.-), sub-classification glycosylases (E.C. 3.2.-.-) and again sub-classification glycosidases (E.C. 3.2.1.-), i.e. enzymes that hydrolyse O- and/or S-glycosyl compounds. Consequently, pectin-cleaving enzymes are effective particularly against residues on dishes which comprise pectic acid and/or other galacturonanes, and catalyze their hydrolysis.
  • enzyme classes Enzyme Commission number
  • the pectin-cleaving enzymes likewise include enzymes with the names pectinase, pectolyase, pectinesterase, pectindemethoxylase, pectinmethoxylase, pectinmethylesterase, pectase, pectinmethylesterase, pectinoesterase, pectinpectylhydrolase, pectindepolymerase, endopolygalacturonase, pectolase, pectinhydrolase, pectin-polygalacturonase, endo-polygalacturonase, poly- ⁇ -1,4-galacturonide glycanohydrolase, endogalacturonase, endo-D-galacturonase, galacturan 1,4- ⁇ -galacturonidase, exopolygalacturonase, poly(galacturonate) hydrolase, exo-D-
  • Exemplary suitable enzymes are available for example under the names Gamanase®, Pektinex AR®, X-Pect® or Pectaway® from Novozymes, under the name Rohapect UF®, Rohapect TPL®, Rohapect PTE100®, Rohapect MPE®, Rohapect MA plus HC, Rohapect DA12L®, Rohapect 10L®, Rohapect B1 L® from AB Enzymes and under the name Pyrolase® from Diversa Corp., San Diego, Calif., USA.
  • hemicellulases can also be incorporated, especially for removing specific problematic soils. These include for example mannanases, xanthanlyases, xanthanases, xyloglucanases, xylanases, pullulanases and ⁇ -glucanases.
  • ⁇ -Giucanase extracted from Bacillus subtilis, is available under the name Cereflo® from the Novozymes Company.
  • Hemicellulases that are inventively particularly preferred are mannanases, e.g. those that are marketed for example under the trade names Mannaway® from the Novozymes Company or Purabrite® from the Genencor Company.
  • a dishwashing composition according to the invention can also comprise oxidoreductases, for example oxidases, oxygenases, catalases (that react at lower H 2 O 2 concentrations than peroxidase), peroxidases, such as halo-, chloro-, bromo-, lignin-, glucose- or manganese-peroxidases, dioxygenases or laccases (phenoloxidases, polyphenoloxidases).
  • oxidoreductases for example oxidases, oxygenases, catalases (that react at lower H 2 O 2 concentrations than peroxidase), peroxidases, such as halo-, chloro-, bromo-, lignin-, glucose- or manganese-peroxidases, dioxygenases or laccases (phenoloxidases, polyphenoloxidases).
  • Suitable commercial products are Denilite® 1 and 2 from the Novozymes Company.
  • Example 1 Adsorption and retention of a polymer according to the present invention (C1) in comparison with the commercially available polymer Mirapol Surf S 110.
  • the copolymer was obtained by reacting 0.08 mol of the above-mentioned monomer mixture, 0.8 mmol AIBN and 0.02 mmol mercapto acetic acid in 81 mL dry DMF after degassing with nitrogen at 70 °C until complete conversion.
  • the polymer was precipitated in cold tert-butyl methyl ether.
  • the phosphate groups were hydrolyzed by dissolving the polymer in 73 mL anhydrous DCM and addition of 0.02 mol trimethyl silyl bromide. The solution was stirred for 24 h at ambient temperature and 50 mL methanol were added and stirred for another 3 h.
  • the resulting polymer was precipitated in cold hexane and dried under vacuum.
  • the resulting copolymer C1 had a number average molecular weight of 5.000 g/mol.
  • Solutions containing 0.3 wt.-% of the copolymer C1 or Mirapol Surf S 110 were obtained by dissolving the polymer in water (16°dH, pH value 3). The obtained solutions were tested for their adsorption value against steel (stainless steel) and SiO 2 via a quartz crystal microbalance (QCM). In the retention measurement the same solutions without polymer were employed to rinse the adsorbates.

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)

Claims (12)

  1. Procédé de production d'un copolymère acrylique phosphoné, comprenant ou consistant en les étapes :
    de réaction
    i) d'au moins un monomère de formule (I)
    Figure imgb0012
     ayant un poids moléculaire moyen en nombre de 250 à 4 000 g/mol avec
    ii) au moins un monomère de formule (II)
    Figure imgb0013
     où
    X représente O ou NH ;
    R1 représente l'hydrogène ou le méthyle ;
    R2 représente un groupe hydrocarboné aliphatique ou aromatique ayant jusqu'à 12 atomes de carbone ;
    R3 et R4 représentent indépendamment choisis parmi l'hydrogène ou un groupe hydrocarboné aliphatique ou aromatique ayant jusqu'à 6 atomes de carbone ; et
    iii) éventuellement jusqu'à 10 % en poids d'au moins un monomère à insaturation éthylénique, sur la base du poids total du mélange de monomères ; éventuellement en présence d'un amorceur radicalaire.
  2. Procédé selon la revendication 1, dans lequel l'au moins un monomère de formule (I) a un poids moléculaire moyen en nombre de 300 à 950 g/mol.
  3. Procédé selon la revendication 1 ou 2, dans lequel dans l'au moins un monomère de formule (II)
    R1 représente un méthyle ; et/ou
    R2 représente un groupe hydrocarboné aliphatique ayant jusqu'à 6 atomes de carbone, de préférence un alkyle en C1 à C4, plus préférablement un méthyle ; et/ou R3 et R4 représentent un hydrogène ou un méthyle ; et/ou
    X représente O.
  4. Procédé selon l'une quelconque des revendications 1 à 3, dans lequel l'au moins un monomère à insaturation éthylénique est choisi parmi le (méth)acrylate en C1 à C12, l'acide acrylique, l'acide méth acrylique, l'acide vinylsulfonique, la vinylpyrrolidone, l'acrylamide, le N-méthyle acrylamide, l'acide maléique, l'anhydride maléique, l'acide itaconique et l'acide cinnamique.
  5. Procédé selon l'une quelconque des revendications 1 à 4, dans lequel l'au moins un monomère de formule (II) est présent dans 0,1 à 99,9 % en moles, de préférence 10 à 50 % en moles et/ou dans lequel l'au moins un monomère de formule (I) est présent dans 0,1 à 99,9 % en moles, de préférence 50 à 90 % en moles.
  6. Procédé selon l'une quelconque des revendications 1 à 5, dans lequel l'amorceur radicalaire est choisi parmi l'azobisisobutyronitrile, le persulfate d'ammonium, le peroxyde d'hydrogène et l'hydroperoxyde de tert-butyle.
  7. Procédé selon l'une quelconque des revendications 1 à 6, dans lequel
    (i) la réaction est effectuée dans un solvant comprenant au moins un alcool en C1-C5 et/ou au moins un solvant hydrocarboné halogéné et/ou de l'eau ; et/ou
    (ii) la réaction est effectuée à des températures de 30 à 100 °C, de préférence de 50 à 80 °C.
  8. Copolymère acrylique phosphoné, pouvant être obtenu par le procédé selon l'une quelconque des revendications 1 à 7.
  9. Colymère acrylique phosphoné selon la revendication 8, dans lequel le copolymère a un poids moléculaire moyen en nombre de 1 000 à 100 000 g/mol, de préférence de 1 500 à 10 000 g/mol.
  10. Utilisation du copolymère acrylique phosphoné selon la revendication 8 ou 9 pour l'hydrophilisation de surfaces, de préférence de surfaces en acier ou de surfaces contenant du silicate.
  11. Composition de lavage de vaisselle, comprenant le copolymère acrylique phosphoné selon la revendication 8 ou 9.
  12. Nettoyage de surfaces dures, composition comprenant le copolymère acrylique phosphoné selon la revendication 8 ou 9.
EP18211842.2A 2018-12-12 2018-12-12 Copolymères acryliques phosphonés pour hydrophilisation de surface Active EP3666872B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP18211842.2A EP3666872B1 (fr) 2018-12-12 2018-12-12 Copolymères acryliques phosphonés pour hydrophilisation de surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP18211842.2A EP3666872B1 (fr) 2018-12-12 2018-12-12 Copolymères acryliques phosphonés pour hydrophilisation de surface

Publications (2)

Publication Number Publication Date
EP3666872A1 EP3666872A1 (fr) 2020-06-17
EP3666872B1 true EP3666872B1 (fr) 2021-08-11

Family

ID=64664970

Family Applications (1)

Application Number Title Priority Date Filing Date
EP18211842.2A Active EP3666872B1 (fr) 2018-12-12 2018-12-12 Copolymères acryliques phosphonés pour hydrophilisation de surface

Country Status (1)

Country Link
EP (1) EP3666872B1 (fr)

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL125864C (fr) * 1959-09-04
DE1801411A1 (de) * 1968-10-05 1970-05-21 Hoechst Ag Gerueststoffe fuer Wasch- und Reinigungsmittel
DE3418496A1 (de) * 1984-05-18 1985-11-21 Hoechst Ag, 6230 Frankfurt Verfahren zur herstellung von mischpolymerisaten aus vinylphosphonsaeure und (meth-)acrylsaeure in waessriger loesung und ihre verwendung
ATE469203T1 (de) 1991-06-11 2010-06-15 Genencor Int Cellulasezusammensetzungen mit einem defizit an komponenten des typs-cbh i enthaltende reinigungsmittelzusammensetzungen
EP0815209B2 (fr) 1995-03-17 2015-02-25 Novozymes A/S Nouvelles endoglucanases
BR9611114A (pt) 1995-10-17 1999-07-13 Rohm Enzyme Finland Oy Celulases os genes codificando-as e os usos das mesmas
DE69735767T2 (de) 1996-09-17 2007-04-05 Novozymes A/S Cellulasevarianten
DE19713852A1 (de) 1997-04-04 1998-10-08 Henkel Kgaa Aktivatoren für Persauerstoffverbindungen in Wasch- und Reinigungsmitteln
EP0877076B1 (fr) * 1997-05-09 2003-11-12 Rohm And Haas Company Compositions détergentes
KR100787392B1 (ko) 1999-03-31 2007-12-21 노보자임스 에이/에스 알칼리 α-아밀라제 활성을 가지는 폴리펩티드 및 그것을코드하는 핵산
PE20010978A1 (es) 1999-12-23 2001-09-14 Upjohn Co ENSAYOS Y METODOS DE DIAGNOSTICO QUE INVOLUCRAN CANALES DE SODIO COMO OBJETIVOS DE AMILOIDE ß O DE SUS AGREGADOS
JP4907834B2 (ja) 2000-08-04 2012-04-04 ダニスコ・ユーエス・インコーポレーテッド 変異体ｅｇｉｉｉセルラーゼ、そのようなｅｇｉｉｉ組成物をコードするｄｎａ及びそれを得るための方法
MXPA03011194A (es) 2001-06-06 2004-02-26 Novozymes As Endo-beta-1,4-glucanasa.
DE10131441A1 (de) 2001-06-29 2003-01-30 Henkel Kgaa Eine neue Gruppe von alpha-Amylasen sowie ein Verfahren zur Identifizierung und Gewinnung neuer alpha-Amylasen
DE10163748A1 (de) 2001-12-21 2003-07-17 Henkel Kgaa Neue Glykosylhydrolasen
DE10260903A1 (de) 2002-12-20 2004-07-08 Henkel Kgaa Neue Perhydrolasen
DK2295554T3 (da) 2003-12-03 2013-03-04 Danisco Us Inc Perhydrolase
DE102004029475A1 (de) 2004-06-18 2006-01-26 Henkel Kgaa Neues enzymatisches Bleichsystem
DE102005059048A1 (de) * 2005-12-08 2007-06-14 Henkel Kgaa Reinigungsmittel für harte Oberflächen
DE102006038448A1 (de) 2005-12-28 2008-02-21 Henkel Kgaa Enzym-haltiges Reinigungsmittel
DE102006022224A1 (de) 2006-05-11 2007-11-15 Henkel Kgaa Subtilisin aus Bacillus pumilus und Wasch- und Reinigungsmittel enthaltend dieses neue Subtilisin
DE102007003143A1 (de) 2007-01-16 2008-07-17 Henkel Kgaa Neue Alkalische Protease aus Bacillus gibsonii und Wasch- und Reinigungsmittel enthaltend diese neue Alkalische Protease
WO2008090152A1 (fr) * 2007-01-22 2008-07-31 Basf Se Procédé de préparation de copolymères de l'acide vinylphosphonique
DE102014206148A1 (de) * 2014-04-01 2015-10-01 Henkel Ag & Co. Kgaa Maschinelles Geschirrspülmittel enthaltend Phosphonopolycarbonsäure

Also Published As

Publication number Publication date
EP3666872A1 (fr) 2020-06-17

Similar Documents

Publication Publication Date Title
US11104867B2 (en) Dishwashing liquid having bleaching catalyst and protease
US10093888B2 (en) Solid dishwashing detergent with improved protease performance
US8349784B2 (en) Automatic dishwashing agent
US7879154B2 (en) Phosphate-free dishwashing detergents comprising builder, bleaching agent, nonionic surfactant, copolymer and a phosphonate
US9752100B2 (en) Detergents
US20100249008A1 (en) Cleaning Agent
US8242068B2 (en) Cleaning agents
KR20100061670A (ko) 세제
CN106795464B (zh) 酶和漂白催化剂的共颗粒
US20120167922A1 (en) Dishwasher detergent
US11220660B2 (en) Portion bag having bleach activator/complexing agent compound
US8551930B2 (en) Dishwasher detergent
EP3292192B1 (fr) Granulé d' enzyme et catalyseur de blanchiment adapté pour des compositions détergentes
EP3666872B1 (fr) Copolymères acryliques phosphonés pour hydrophilisation de surface
US20120178663A1 (en) Dishwasher detergent
US20220251475A1 (en) Dishwashing agent with bleaching catalyst and bacillus gibsonii protease
WO2012143315A1 (fr) Détergent sans phosphates pour lave-vaisselle

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

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

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20181212

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

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

Free format text: STATUS: GRANT OF PATENT IS INTENDED

RIC1 Information provided on ipc code assigned before grant

Ipc: C11D 3/00 20060101ALI20210407BHEP

Ipc: C11D 3/37 20060101AFI20210407BHEP

INTG Intention to grant announced

Effective date: 20210422

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

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

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602018021568

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Ref country code: AT

Ref legal event code: REF

Ref document number: 1419399

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210915

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20210811

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1419399

Country of ref document: AT

Kind code of ref document: T

Effective date: 20210811

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

Ref country code: HR

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

Effective date: 20210811

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: 20210811

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: 20210811

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: 20210811

Ref country code: RS

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

Effective date: 20210811

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: 20210811

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: 20211111

Ref country code: LT

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

Effective date: 20210811

Ref country code: NO

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

Effective date: 20211111

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: 20211213

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

Ref country code: PL

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

Effective date: 20210811

Ref country code: LV

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

Effective date: 20210811

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: 20211112

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: 20210811

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

Ref country code: DK

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

Effective date: 20210811

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602018021568

Country of ref document: DE

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

Ref country code: SM

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

Effective date: 20210811

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: 20210811

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: 20210811

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: 20210811

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: 20210811

Ref country code: AL

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

Effective date: 20210811

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

26N No opposition filed

Effective date: 20220512

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

Effective date: 20210811

Ref country code: IT

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

Effective date: 20210811

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: 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: 20210811

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20211231

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: 20211212

Ref country code: IE

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

Effective date: 20211212

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 NON-PAYMENT OF DUE FEES

Effective date: 20211231

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: 20211231

Ref country code: CH

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

Effective date: 20211231

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: 20210811

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

Effective date: 20230530

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; INVALID AB INITIO

Effective date: 20181212

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

Ref country code: GB

Payment date: 20231220

Year of fee payment: 6

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

Ref country code: FR

Payment date: 20231222

Year of fee payment: 6

Ref country code: DE

Payment date: 20231214

Year of fee payment: 6

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

Ref country code: MK

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

Effective date: 20210811

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

Ref country code: MT

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

Effective date: 20210811