WO2015000744A1 - Process for cleaning dishware - Google Patents

Process for cleaning dishware Download PDF

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Publication number
WO2015000744A1
WO2015000744A1 PCT/EP2014/063279 EP2014063279W WO2015000744A1 WO 2015000744 A1 WO2015000744 A1 WO 2015000744A1 EP 2014063279 W EP2014063279 W EP 2014063279W WO 2015000744 A1 WO2015000744 A1 WO 2015000744A1
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WO
WIPO (PCT)
Prior art keywords
meth
weight
range
acid
comonomer
Prior art date
Application number
PCT/EP2014/063279
Other languages
French (fr)
Inventor
Holger TÜRK
Heike Weber
Jürgen Detering
Gazi TÜRKOGLU
Original Assignee
Basf Se
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 Basf Se filed Critical Basf Se
Priority to RU2016103485A priority Critical patent/RU2016103485A/en
Priority to EP14731978.4A priority patent/EP3017030A1/en
Priority to US14/902,776 priority patent/US9938489B2/en
Priority to KR1020167003198A priority patent/KR20160030256A/en
Priority to CN201480037687.4A priority patent/CN105358669A/en
Priority to JP2016522443A priority patent/JP2016530348A/en
Publication of WO2015000744A1 publication Critical patent/WO2015000744A1/en

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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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • C11D1/721End blocked ethers
    • AHUMAN NECESSITIES
    • A47FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47LDOMESTIC WASHING OR CLEANING; SUCTION CLEANERS IN GENERAL
    • A47L15/00Washing or rinsing machines for crockery or tableware
    • A47L15/0002Washing processes, i.e. machine working principles characterised by phases or operational steps
    • A47L15/0007Washing phases
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/0065Solid detergents containing builders
    • C11D17/0073Tablets
    • C11D17/0091Dishwashing tablets
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2082Polycarboxylic acids-salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2086Hydroxy carboxylic acids-salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/33Amino carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3761(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
    • C11D2111/14

Definitions

  • the present invention is directed towards a process for cleaning dishware soiled with fatty residue, characterized in that said process is carried out at a temperature in the range of from 45 to 65°C and using at least one formulation, comprising
  • R 1 being selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C3o-alkenyl, straight-chain or branched, with at least one C-C double bond,
  • R 2 being selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C3o-alkenyl, straight-chain or branched, with at least one C-C double bond, x being selected from one to 100,
  • AO being identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (Chb O, CH 2 CH(CH 3 )-0, CH(CH 3 )-CH 2 -0- and CH 2 CH(n-C 3 H 7 )-0, percentages being based on the total solids content of said formulation.
  • the present invention is directed towards formulations that are useful for cleaning dishware, and towards a process for making such formulations.
  • Detergent formulations especially detergent formulations for automatic dishwashing, have to meet various requirements.
  • such detergent formulations need to enable a complete cleaning of china, polymer, metal, clay, and glassware and to remove all sorts of soil, like fat, proteins, starch, dyes, and more.
  • the soils need to be dispersed in water during the cleaning and the water removal process, and the various soils should not deposit in the dishwashing machine in case of automatic dishwashing.
  • the cleaned good should exhibit a good drying behavior, without spotting.
  • Mixed hydroxy ethers are particularly efficient non-ionic surfactants, especially when combined with certain polymers, see, e. g., WO 2008/095563.
  • WO 2008/095563 especially the use of mixed hydroxy ethers in formulations disclosed in WO 2008/095563 in automatic dishwashers can lead to rather high amounts of surfactant and fat residues in the filters or sieves.
  • the inventive process is a process for cleaning dishware.
  • the inventive process can be carried out either manually (hand-dish-wash) or preferably with the help of a machine (machine dish- wash or automatic dish-wash).
  • Dishes in the context of the present invention shall not only refer to plates from china but also to any kitchenware from china, metal, glass, clay or polymer, such as - but not limited to - cups, bowls and plates from china, flatware, drinking glasses such as wine glasses, champagne flutes, beer glasses and the like, and plastic kitchenware, furthermore pots, frying pans and Dutch ovens from metal such as iron, aluminum or stainless steel.
  • Dish-ware is provided in soiled form, among other soiled with fatty residue, also referred to as fat, that may stem from food itself or - for example in the case of frying pans - fat that stems from cooking or frying or baking food.
  • fat may also include lard or oil, especially oil like sunflower oil, olive oil or other oil that is used for cooking purposes.
  • Said fatty residue may be the sole soiling of dishware to be cleaned according to the inventive process.
  • dish-ware to be cleaned according to inventive process may be soiled with a combination of fat and at least one substance other than fat, for example pigment(s), protein, carbohydrates such as starch or sugar, caramel, further- more lecithin, or dyestuff(s).
  • the inventive process is being carried out at temperatures in the range of from 45 to 65°C, preferably 50 to 60°C. Said temperature refers to the temperature of the water being used in the inventive process. The inventive process is being described in more detail below.
  • the inventive process is being carried out using water.
  • the amount of water is influenced by the type of machine used and by the choice of the program.
  • Formulations used in the inventive process comprise
  • complexing agent (A) in the range of from 1 to 50 % by weight, preferably 10 to 40 % by weight of at least one complexing agent, hereinafter also being referred to as complexing agent (A), said com- plexing agent being selected from the alkali metal salts of citric acid, from the alkali metal salts of aminocarboxylic acids and from sodium tripolyphosphate.
  • alkali metal salts in the context of complexing agent (A) are the potassium salts and in particular the sodium salts.
  • Preferred alkali metal salts of citric acid are the sodium salts, especially the trisodium salt.
  • aminocarboxylic acids are methylglycine diacetic acid (MGDA), glutamic acid diacetic acid (GLDA) and iminodisuccinic acid (IDS).
  • Preferred alkali metal salts of aminocarboxylic acids are the trisodium salt of MGDA, the tetrasodium salt of GLDA and the tetra- sodium salt of IDS.
  • Sodium tripolyphosphate preferably refers to the respective pentasodium salt.
  • said formulation may contain a combination of at least two complexing agents (A), such as, for example, a combination of alkali metal salts of citric acid and MGDA, or of citric acid and GLDA, or combinations of alkali metal salts of citric acid and sodium tripolyphosphate.
  • A complexing agents
  • Preferred are combinations of the respective sodium salts, in particular combinations of the trisodium salts of citric acid and MGDA.
  • formulations used in the inventive process are phosphate-free.
  • the term phosphate-free refers to a combined phosphate and polyphosphate content of 0.01 or less up to 0.5% by weight of phosphate.
  • Formulations used in the inventive process further comprise
  • surfactant (B) in the range of from 2 to 8 % by weight, preferably up to 6 % by weight of at least one non- ionic surfactant of general formula (I) R 1 -CH(OH)-CH 2 -0-(AO)x-R 2 (I), hereinafter also being referred to as "surfactant (B)", the integers being defined as follows:
  • R 1 is selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C4-C3o-alkyl, straight- chain or branched, more preferred is straight-chain C4-C3o-alkyl and even more preferred is n-Cio-Ci2-alkyl.
  • R 2 is selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C6-C2o-alkyl, more preferred is Cs-Cn-alkyl, x is selected from one to 100, preferably from 5 to 60, more preferably 10 to 50, and even more preferably 20 to 40,
  • AO is selected from identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (CH 2 )4-0, CH 2 CH(CH 3 )-0, CH(CH 3 )-CH 2 -0- and CH 2 CH(n-C 3 H 7 )-0.
  • (AO) x is selected from (ChbChbOJxi, x1 being selected from one to 50.
  • (AO) x is selected from
  • x or x1 or x2 and x3 or x4 are to be understood as average values, the number average being preferred. Therefore, each x or x1 or x2 or x3 or x4 - if applicable - can refer to a fraction although a specific molecule can only carry a whole number of alkylene oxide units.
  • Formulations used in the inventive process further comprise
  • copolymer (C) in the range of from 0.25 to less than 4 %, preferably 0.5 to 3.5% by weight of a copolymer, hereinafter also being referred to as copolymer (C), being obtained from copolymerizing the following comonomers (a) at least one comonomer, also being referred to as "comonomer (a)", selected from eth- ylenically unsaturated C3-C4-carboxylic acids, for example crotonic acid and preferably (meth)acrylic acid, (E)-crotonic acid, (Z)-crotonic acid, preferred is methacrylic acid and even more preferred is acrylic acid, and from ethylenically unsaturated C4-C8- dicarboxylic acids and their respective anhydrides, for example maleic acid, maleic an- hydride, itaconic acid, itaconic anhydride, citraconic acid, metaconic anhydride and fu- maric acid, preferred is maleic
  • comonomer (b) at least one comonomer, also referred to as “comonomer (b)", being selected from isobutene, diisobutene,
  • CisH37-ester (meth)acrylic acid n-C2oH4i-ester, (meth)acrylic acid n-C22H45-ester and (meth)acrylic acid n-C24H49-ester.
  • (c) optionally, at least one further comonomer, also being referred to as "comonomer (c)", such comonomer (c) being selected from non-ionic comonomers and being different from both comonomer (a) and comonomer (b) and not being selected from either group of comonomers (a) and (b).
  • comonomer (c) being selected from non-ionic comonomers and being different from both comonomer (a) and comonomer (b) and not being selected from either group of comonomers (a) and (b).
  • Percentages of complexing agent (A), surfactant (B) and copolymer (C) are percentages by weight and refer to the total solids content of the respective formulation.
  • copolymer (C) can be obtained by free radical co- polymerization.
  • comonomer (c) is selected from omethyl styrene, para-methyl styrene and preferably from styrene.
  • AO is being defined as above.
  • y and y1 and y2 are to be understood as average values, the number average being preferred. Therefore, each y or y1 or y2 - if applicable - can refer to a fraction although a specific molecule can only carry a whole number of alkylene oxide units.
  • copolymer (C) has an average molecular weight Mw in the range of from 1 ,000 to 30,000 g/mol, preferably 2,000 to 10,000 g/mol, determined, for example, by gel permeation chromatography (GPC) or size exclusion chromatography, and referring to the acid/salt.
  • Mw average molecular weight
  • copolymer (C) exhibits a polydispersity M w /M n in the range of from 1 .5 to 10, preferably 2 to 5.
  • copolymer (C) is used as its alkali metal salt, its carboxyl groups being partially or preferably fully neutralized with alkali, preferably with sodium.
  • copolymer (C) is selected from random copolymers, alternating copolymers, block copolymers and multiblock copolymers.
  • comonomer (a) is selected from maleic acid and maleic anhydride and comonomer (b) is selected from isobutene, diisobutene and C2-C28-0 olefins, preferably from straight-chain C2-C28-a-olefins.
  • Such copolymers (C) are preferably alternating copolymers.
  • comonomer (a) is selected from (meth)acrylic acid and comonomer (b) is selected from Ci2-C24-alkyl esters of (meth)acrylic acid.
  • Such copol- ymers (C) are preferably random copolymers.
  • copolymer (C) is made from
  • comonomer(s) (b) selected from isobutene, diisobutene, and C2-C28-a-olefins, and, optionally
  • copolymer (C) is made from
  • comonomer(s) (b) selected from Ci2-C24-alkyl esters of (meth)acrylic acid, and, optionally
  • Percentages are referring to the total respective copolymer (C) as free acid.
  • formulations used in the inventive process may have a total solids content in the range of from 90 to 99.9%, preferably 95 to 99 % by weight.
  • inventive formulations are, e. g., in the form of powder or tablets.
  • formulations used in the inventive process may have a total solids content in the range of from 15 to 40% by weight.
  • inventive formulations are, e. g., in the form of gels.
  • the inventive process comprises several steps, one of the steps being contacting the soiled dishware with a formulation as disclosed above, and also comprising at least one rinsing step and at least one drying step.
  • the formulation used in the inventive process can be used as 2-in-1 or 3-in-1 formulation, and no separate rinse agent is necessary.
  • the ion exchange does not need to be treated with regenerating salt.
  • the formulation used in the inventive process can be used as 2-in-1 or 3-in-1 formulation, and neither a separate rinse agent nor a regenerating salt is necessary.
  • formulations used in the inventive process may contain at least one further ingredient, also being referred to as ingredient (D).
  • Ingredient (D) may be selected from one or more surfactants other than surfactant (B), one or more enzymes, one or more builders other than complexing agent (A), in particular phosphorus-free builders, one or more cobuilders, one or more alkali carriers, one or more bleaching agents, one or more bleach catalysts, one or more bleach activators, one or more bleach stabilizers, one or more antifoams, one or more corrosion inhibitors, one or more buffer or one or more dyes.
  • surfactants other than surfactant (B) are in particular nonionic surfactants other than surfactant (B) as well as mixtures of anionic or zwitterionic surfactants with nonionic surfactants other than surfactant (B).
  • Preferred nonionic surfactants other than surfactant (B) are alkoxylated alcohols and alkoxylated fatty alcohols, di- and multiblock copolymers of ethylene oxide and propylene oxide and reaction products of sorbitan with ethylene oxide or propylene oxide, alkyl glycosides and so-called amine oxides.
  • alkoxylated alcohols and alkoxylated fatty alcohols are, for example, compounds of the general formula (II)
  • R 5 is selected from Cs-C22-alkyl, for example n-CsH , n-doHb-i , n-Ci2H25, n-C-uHbsi, n-Ci6H33
  • n and n are in the range from zero to 300, where the sum of n and m is at least one.
  • m is in the range from 1 to 100 and n is in the range from 0 to 30.
  • Compounds of the general formula (II) may be block copolymers or random copolymers, preference being given to block copolymers.
  • alkoxylated alcohols and alkoxylated fatty alcohols are, for exam- pie, compounds of the general formula (III)
  • R 6 is selected from C6-C2o-alkyl, in particular n-CsH , n-doHb-i , n-Ci2H25, n-C-uFbs), n-Ci6H33,
  • a is a number in the range from 1 to 6
  • b is a number in the range from 4 to 20
  • d is a number in the range from 4 to 25.
  • Compounds of the general formula (III) may be block copolymers or random copolymers, preference being given to block copolymers.
  • nonionic surfactants are selected from di- and multiblock copolymers, composed of ethylene oxide and propylene oxide. Further suitable nonionic surfactants are selected from ethoxylated or propoxylated sorbitan esters. Amine oxides or alkyl glycosides are likewise suitable. An overview of suitable further nonionic surfactants can be found in EP-A 0 851 023 and in DE-A 198 19 187.
  • Mixtures of two or more different nonionic surfactants other than surfactant (B) may also be present.
  • anionic surfactants are Cs-C2o-alkyl sulfates, C8-C20-alkylsulfonat.es and C8-C20- alkyl ether sulfates with one to 6 ethylene oxide units per molecule.
  • formulations used in the inventive process can comprise in the range from 3 to 20% by weight of surfactant other than surfactant (B).
  • Formulations used in the inventive process can comprise one or more enzymes. Examples of enzymes are lipases, hydrolases, amylases, proteases, cellulases, esterases, pectinases, lactases and peroxidases.
  • Formulations used in the inventive process can comprise, for example, up to 5% by weight of enzyme, preference being given to 0.1 to 3% by weight, in each case based on the total solids content of the formulation according to the invention.
  • formulations used according to the invention can com- prise one or more builders, in particular phosphate-free builders.
  • suitable builders are fatty acid sulfonates, ohydroxypropionic acid, alkali metal malonates, fatty acid sulfonates, alkyl and alkenyl disuccinates, tartaric acid diacetate, tartaric acid monoacetate, oxidized starch, and polymeric builders, for example polycarboxylates and polyaspartic acid.
  • builders are selected from polycarboxylates, for example alkali metal salts of (meth)acrylic acid homopolymers or (meth)acrylic acid copolymers.
  • Suitable comonomers of polycarboxylates are monoethylenically unsaturated dicarboxylic acids such as maleic acid, fumaric acid, maleic anhydride, itaconic acid and citraconic acid.
  • a suitable (meth)acrylic acid homopolymer is in particular polyacrylic acid, which preferably has an average molecular weight M w in the range from 2,000 to 40,000 g/mol, preferably 2,000 to 10,000 g/mol, in particular 3,000 to 8,000 g/mol.
  • copolymeric polycarboxylates in particular those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid and/or fumaric acid.
  • Formulations used according to the invention can comprise, for example, in the range from in total 2.5 to 20% by weight, preferably up to 10% by weight, of builders other than complexing agent (A).
  • formulations used according to the invention can comprise one or more cobuilders.
  • cobuilders are phosphonates, for example hydroxyalkanephosphonates and ami- noalkanephosphonates.
  • hydroxyalkanephosphonates 1 -hydroxyethane-1 ,1 - diphosphonate (HEDP) is of particular importance as a cobuilder.
  • HEDP 1 -hydroxyethane-1 ,1 - diphosphonate
  • HEDP ethylenediaminetetra- methylenephosphonate
  • DTPMP diethylenetriaminepentamethylenephosphonate
  • amphoteric polymers can also be used as cobuilders.
  • Formulations used in the inventive process can comprise one or more alkali carriers.
  • Alkali carriers ensure, for example, a pH of at least 9 if an alkaline pH is desired.
  • alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydroxides and alkali metal metasilicates are particularly preferred.
  • a preferred alkali metal is in each case potassium, particular preference being given to sodium.
  • Formulations used in the inventive process can comprise one or more bleach catalysts.
  • Bleach catalysts can be selected from bleach-boosting transition metal salts or transition metal complexes such as, for example, manganese-, iron-, cobalt-, ruthenium- or molybdenum-salen complexes or carbonyl complexes.
  • Manganese, iron, cobalt, ruthenium, molybdenum, titanium, vanadium and copper complexes with nitrogen-containing tripod ligands and also cobalt-, iron-, copper- and ruthenium-amine complexes can also be used as bleach catalysts.
  • Formulations used in the inventive process can comprise, for example, 0.5 to 15% by weight of bleaching agents, hereinafter also referred to as bleach (D).
  • Bleach (D) can be selected from oxygen bleaches and chlorine-containing bleaches.
  • oxygen bleaches are sodium perborate, anhydrous or for example as monohydrate or as tetrahydrate or so-called dihydrate, sodium percarbonate, anhydrous or, for example, as monohydrate, hydrogen peroxide, persulfates, organic peracids such as peroxylauric acid, peroxystearic acid, peroxy-a-naphthoic acid, 1 ,12-diperoxydodecanedioic acid, per- benzoic acid, peroxylauric acid, 1 ,9-diperoxyazelaic acid, diperoxyisophthalic acid, in each case as free acid or as alkali metal salt, in particular as sodium salt, also sulfonylperoxy acids and cationic peroxy acids.
  • Formulations used in the inventive process can comprise, for example, in the range from 0.5 to 15% by weight of oxygen bleach.
  • Suitable chlorine-containing bleaches are, for example, 1 ,3-dichloro-5,5-dimethylhydantoin, N- N-chlorosulfamide, chloramine T, chloramine B, sodium hypochlorite, calcium hypochlorite, magnesium hypochlorite, potassium hypochlorite, potassium dichloroisocyanurate and sodium dichloroisocyanurate.
  • Formulations used in the inventive process can preferably comprise, for example, in the range from 3 to 10% by weight of chlorine-containing bleach.
  • Formulations used in the inventive process can comprise one or more bleach activators, for example N-methylmorpholinium-acetonitrile salts ("MMA salts”), trimethylammonium acetonitrile salts, N-acylimides such as, for example, N-nonanoylsuccinimide, 1 ,5-diacetyl-2,2- dioxohexahydro-1 ,3,5-triazine (“DADHT”) or nitrile quats (trimethylammonium acetonitrile salts).
  • suitable bleach activators are tetraacetylethylenediamine (TAED) and tetraacetylhexylenediamine.
  • Formulations used in the inventive process can comprise one or more corrosion inhibitors.
  • corrosion inhibitors include triazoles, in particular benzotria- zoles, bisbenzotriazoles, aminotriazoles, alkylaminotriazoles, also phenol derivatives such as, for example, hydroquinone, pyrocatechol, hydroxyhydroquinone, gallic acid, phloroglucinol or pyrogallol.
  • formulations used in the inventive process comprise in total in the range from 0.1 to 1.5% by weight of corrosion inhibitor.
  • Formulations used in the inventive process can comprise one or more fillers, for example sodi- urn sulfate.
  • Formulations used in the inventive process can comprise one or more antifoams, selected for example from silicone oils and paraffin oils.
  • formulations used in the inventive process comprise in total in the range from 0.05 to 0.5% by weight of antifoam.
  • Dishware cleaned according to the inventive process exhibits excellent properties, such as very good removal of soiling, especially of fat. Furthermore, dishware cleaned according to the in- ventive process show excellent values for spotting, filming and residues. In addition, when modern dishwashing machines are used, the filter(s) and/or sieves will contain only very low amounts of surfactant and fat after operation.
  • inventive formulations may be unit doses, such as tablets, or as gel or powder, as granules or compactate. In a preferred embodiment, such a unit dose comprises 10 to 30 g of inventive formulation.
  • inventive formulations may be solid, and in such embodiments they may contain some residual humidity, such as 0.01 to 10 % by weight, water. In other embodiments, inventive formulations may be liquids or gels.
  • Inventive formulations comprise
  • (A) in the range of from 1 to 50 % by weight, preferably 10 to 40 % by weight of at least one complexing agent (A), said complexing agent being selected from the alkali metal salts of citric acid, from the alkali metal salts of aminocarboxylic acids and from sodium tripolyphosphate.
  • alkali metal salts in the context of complexing agent (A) are the potassium salts and in particular the sodium salts.
  • Preferred alkali metal salts of citric acid are the sodium salts, especially the trisodium salt.
  • aminocarboxylic acids are methylglycine diacetic acid (MGDA), glutamic acid diacetic acid (GLDA) and iminodisuccinic acid (IDS).
  • Preferred alkali metal salts of aminocarboxylic acids are the trisodium salt of MGDA, the tetrasodium salt of GLDA and the tetra- sodium salt of IDS.
  • Sodium tripolyphosphate preferably refers to the respective pentasodium salt.
  • inventive formulations may contain a combination of at least two complexing agents (A), such as, for example, a combination of alkali metal salts of citric acid and MGDA, or of citric acid and GLDA, or combinations of alkali metal salts of citric acid and sodium tripolyphosphate.
  • A complexing agents
  • Preferred are combinations of the respective sodium salts, in particular combinations of the trisodium salts of citric acid and MGDA.
  • inventive formulations are phosphate-free.
  • phosphate-free refers to a combined phosphate and polyphosphate content of 0.01 or less up to 0.5% by weight of phosphate.
  • Inventive formulations further comprise
  • R 1 is selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C4-C3o-alkyl, straight- chain or branched, more preferred is straight-chain C4-C3o-alkyl and even more preferred is n-Cio-Ci2-alkyl.
  • x is selected from one to 100, preferably from 5 to 60, more preferably 10 to 50, and even more preferably 20 to 40,
  • AO is selected from identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (CH 2 )4-0, CH 2 CH(CH 3 )-0, CH(CH 3 )-CH 2 -0- and CH 2 CH(n-C 3 H 7 )-0.
  • CH2-CH2-O alkylene oxides
  • (AO) x is selected from , x1 being selected from one to 50.
  • (AO) x is selected from -(ChbCI-bO ⁇ - (CH2CH(CH3)-0)x3, x2 and x3 being identical or different and selected from 1 to 30.
  • Inventive formulations further comprise (C) in the range of from 0.25 to less than 4 %, preferably 0.5 to 3.5% by weight of copolymer (C), being obtained from copolymerizing the following comonomers
  • comonomer (c) being different from both comonomer (a) and comonomer (b) and not being selected from either group of comonomers (a) and (b).
  • Percentages of complexing agent (A), surfactant (B) and copolymer (C) are percentages by weight and refer to the total solids content of the respective formulation.
  • Comonomers (a), (b) and (c) have been defined above.
  • inventive formulations are phosphate-free.
  • copolymer (C) has an average molecular weight Mw in the range of from 1 ,000 to 30,000 g/mol, preferably up to 10,000 g/mol, determined by GPC. In one embodiment of the present invention, copolymer (C) exhibits a polydispersity M w /M n in the range of from 1.5 to 10, preferably 2 to 5.
  • copolymer (C) is used as its alkali metal salt, its carboxyl groups being partially or preferably fully neutralized with alkali, preferably with sodium.
  • copolymer (C) is selected from random copolymers, alternating copolymers, block copolymers and multiblock copolymers.
  • comonomer (a) is selected from maleic acid and maleic anhydride and comonomer (b) is selected from isobutene, diisobutene and C2-C28-0 olefins, preferably from straight-chain C2-C28-a-olefins.
  • Such copolymers (C) are preferably alternating copolymers.
  • comonomer (a) is selected from (meth)acrylic acid and comonomer (b) is selected from Ci2-C24-alkyl esters of (meth)acrylic acid.
  • Such copolymers (C) are preferably random copolymers.
  • inventive formulations have a total solids content in the range of from 90 to 99.9%, preferably 95 to 99 % by weight. Such inventive formulations are, e. g., in the form of powder or tablets. In one embodiment of the present invention, inventive formulations have a total solids content in the range of from 15 to 40% by weight. Such inventive formulations are, e. g., in the form of gels. In one embodiment of the present invention, inventive formulations may contain at least one further ingredient, also being referred to as ingredient (D).
  • Ingredient (D) may be selected from one or more surfactants other than surfactant (B), one or more enzymes, one or more builders other than complexing agent (A), in particular phosphorus-free builders, one or more cobuilders, one or more alkali carriers, one or more bleaching agents, one or more bleach catalysts, one or more bleach activators, one or more bleach stabilizers, one or more antifoams, one or more corrosion inhibitors, one or more buffer or one or more dyes. Ingredients (D) have been explained in more detail above.
  • Inventive formulations are excellently suitable for carrying out the inventive process.
  • a further aspect of the present invention is a process for making inventive formulations, hereinafter also being referred to as inventive manufacturing process.
  • the inventive manufacturing process comprises mixing complexing agent (A), surfactant (B) and copolymer (C) and, if applicable, one or more further ingredient (D), in one or more steps.
  • Such mixing can be performed in the absence or presence of water, preferably mixing is being performed in the absence of water.
  • at least one of the components complexing agent (A), surfactant (B) and copolymer (C) or, if applicable, one or more further ingredient (D) is added as aqueous solution to other components that are powdery or in the form of granules, and the water is being removed during or after mixing.
  • Mixing can be performed at a temperature in the range of from 5 to 100°C, preferably 20 to 70°C or at ambient temperature.
  • the inventive manufacturing process is being carried out in the presence of water, and such water is at least partially removed at the end of the inventive manufacturing process, for example by spray-drying or by making compactates of granules of different components or of premixed components.
  • Copolymer (C.1 ): fully neutralized sodium salt of random copolymer from maleic acid anhydride (a.1 ), CH 2 CH-n-Ci 6 H 3 3 (b.1 )/isobutene (b.2); 65 % by weight of (a.1 ), 9 % by weight of (b.1 ), 26 % by weight of (b.2), percentages referring to the respective free acid of (C.1 ) Synthesis of copolymer (C.1 ):
  • O-Xylene (363 g) and maleic acid anhydride (a.1 ) (196 g) were placed in an autoclave equipped with metering and distillation devices and a stirrer.
  • the autoclave was purged with 3 bar of nitrogen three times.
  • the pressure was then reduced to 91 mbar and the mixture of (a.1 ) and o- xylene was heated to 120°C.
  • the following feeds were added simultaneously at 120°C, each with constant rate , starting at the same time:
  • Copolymer (C.2) fully neutralized sodium salt of random copolymer from acrylic acid
  • a polymerization vessel equipped with an anchor stirrer and metering devices was charged with a solution of 5 g od acrylic acid (a.2) in 175 g of isopropanol. The mixture was heated to 80°C under an atmosphere of nitrogen. The following feeds were added simultaneously at 80°C, each with constant rate, starting at the same time:
  • the pH value of aqueous mix- ture so obtained was adjusted to 7.0 with aqueous sodium hydroxide solution to yield a clear aqueous polymer solution with a solid content of 23.2 wt.%. M w : 5180 g/mol.
  • the weight-average molecular weight (M w ) of copolymer (C.2) was determined by GPC (gel permeation chromatography) at 23 °C, using a PSS Suprema column (PSS, Mainz, Germany).
  • the eluent employed was an aqueous tris(hydroxymethyl)amino methane (TRIS) buffer solution (0.02 M), containing 0.2 M sodium chloride.
  • TIS tris(hydroxymethyl)amino methane
  • base mixtures were prepared from the feed materials according to table 1.
  • the feed materials as well as copolymer (C.1 ), copolymer (C.2) and/or polymer (D.3) were mixed in dry state apart from (B.1 ) and (B.2), which were finally added in molten form.
  • “Sieves (grade)” refers to an average grade. The sieves and filters only contained very little fat and detergent when TF.2 was used. When C-TF.1 was used, soiling of the sieve could be ob- served after the 6 th cycle.
  • “Sieves (grade)” refers to an average grade. The sieves and filters only contained very little fat and detergent when TF.4 or TF.5 was used. When C-TF.3 was used, strong soiling of the sieve could be observed after the 30 th cycle.
  • copolymer (C.2) was used instead of copolymer (C.1 ) the same trend was observed.

Abstract

Process for cleaning dishware soiled with fatty residue, characterized in that said process is carried out at a temperature in the range of from 45 to 65°C and using at least one formulation, comprising (A) in the range of from 1 to 50 % by weight of at least one complexing agent, selected from the alkali metal salts of citric acid, aminocarboxylic acids and from sodium tripolyphosphate, (B) in the range of from 2 to 8 % by weight of at least one non-ionic surfactant of general formula (I) R1-CH(OH)-CH2-O-(AO)x-R2 (I) (C) in the range of from 0.25 to less than 4 % by weight of a copolymer, being obtained from copolymerizing the following comonomers (a) at least one comonomer selected from ethylenically unsaturated C3-C4-carboxylic acids and ethylenically unsaturated C4-C8-dicarboxylic acids or their respective anhydrides, (b) at least one comonomer selected from isobutene, diisobutene, C2-C28-a-olefins, and C12-C24-alkyl esters of (meth)acrylic acid, (c) optionally, at least one further comonomer selected from non-ionic comonomers, the integers being defined as follows: R1 being selected from C4-C30-alkyl, straight-chain or branched, and from C4-C30-alkenyl, straight-chain or branched, with at least one C-C double bond, R2 being selected from C1-C30-alkyl, straight-chain or branched, and from C2-C30-alkenyl, straight-chain or branched, with at least one C-C double bond, x being selected from one to 100, AO being identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-O, (CH2)4-O, CH2CH(CH3)-O, CH(CH3)-CH2-O- and CH2CH(n-C3H7)-O.

Description

Process for cleaning dishware
The present invention is directed towards a process for cleaning dishware soiled with fatty residue, characterized in that said process is carried out at a temperature in the range of from 45 to 65°C and using at least one formulation, comprising
(A) in the range of from 1 to 50 % by weight of at least one complexing agent, selected from the alkali metal salts of citric acid, aminocarboxylic acids and from sodium tripolyphos- phate,
(B) in the range of from 2 to 8 % by weight of at least one non-ionic surfactant of general formula (I)
R -CH(OH)-CH2-0-(AO)x-R2 (I)
(C) in the range of from 0.25 to less than 4 % by weight of a copolymer, being obtained from copolymerizing the following comonomers
(a) at least one comonomer selected from ethylenically unsaturated C3-C4-carboxylic acids and ethylenically unsaturated C4-C8-dicarboxylic acids or their respective anhydrides,
(b) at least one comonomer selected from isobutene, diisobutene, C2-C28-a-olefins, and C12- C24-alkyl esters of (meth)acrylic acid,
(c) optionally, at least one further comonomer selected from non-ionic comonomers, the integers being defined as follows:
R1 being selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C3o-alkenyl, straight-chain or branched, with at least one C-C double bond,
R2 being selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C3o-alkenyl, straight-chain or branched, with at least one C-C double bond, x being selected from one to 100,
AO being identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (Chb O, CH2CH(CH3)-0, CH(CH3)-CH2-0- and CH2CH(n-C3H7)-0, percentages being based on the total solids content of said formulation.
Furthermore, the present invention is directed towards formulations that are useful for cleaning dishware, and towards a process for making such formulations. Detergent formulations, especially detergent formulations for automatic dishwashing, have to meet various requirements. When being used in automatic dishwashing, such detergent formulations need to enable a complete cleaning of china, polymer, metal, clay, and glassware and to remove all sorts of soil, like fat, proteins, starch, dyes, and more. The soils need to be dispersed in water during the cleaning and the water removal process, and the various soils should not deposit in the dishwashing machine in case of automatic dishwashing. Finally, during the drying process, the cleaned good should exhibit a good drying behavior, without spotting. It has been found that in many cases fatty residues are being accumulated in the fat filter or sieves of automatic dishwashing machines. Such residues usually contain surfactant and fat which has been removed from the dishware, or degradation products from soil. The deposition of residues is disadvantageous because such filters or sieves need cleaning when filled with surfactant and fat. Furthermore, such fatty residues may become smelly in case the machine is not in use for some time, and they may even become a hygiene hazard.
Mixed hydroxy ethers are particularly efficient non-ionic surfactants, especially when combined with certain polymers, see, e. g., WO 2008/095563. However, especially the use of mixed hydroxy ethers in formulations disclosed in WO 2008/095563 in automatic dishwashers can lead to rather high amounts of surfactant and fat residues in the filters or sieves.
It was therefore an objective of the present invention to provide a method for cleaning dishware soiled with fat without having to cope with significant residues of surfactant and fat in the filters or sieves of the dishwashing machine but not loss on quality of the dishwashing process. Fur- thermore, it was an objective to provide formulations useful for cleaning dishware soiled with fat without having to cope with significant residues of surfactant and fat in the filters or sieves of the dishwashing machine but not loss on quality of the dishwashing process. Furthermore, it was an objective to provide a method for making such formulations. Accordingly, the processes and formulations defined in the outset have been found. Firstly, the process defined in the outset, hereinafter also referred to as inventive process, will be defined in more detail.
The inventive process is a process for cleaning dishware. The inventive process can be carried out either manually (hand-dish-wash) or preferably with the help of a machine (machine dish- wash or automatic dish-wash). Dishes in the context of the present invention shall not only refer to plates from china but also to any kitchenware from china, metal, glass, clay or polymer, such as - but not limited to - cups, bowls and plates from china, flatware, drinking glasses such as wine glasses, champagne flutes, beer glasses and the like, and plastic kitchenware, furthermore pots, frying pans and Dutch ovens from metal such as iron, aluminum or stainless steel.
Dish-ware is provided in soiled form, among other soiled with fatty residue, also referred to as fat, that may stem from food itself or - for example in the case of frying pans - fat that stems from cooking or frying or baking food. The term "fat" may also include lard or oil, especially oil like sunflower oil, olive oil or other oil that is used for cooking purposes. Said fatty residue may be the sole soiling of dishware to be cleaned according to the inventive process. In another embodiment of the present invention, dish-ware to be cleaned according to inventive process may be soiled with a combination of fat and at least one substance other than fat, for example pigment(s), protein, carbohydrates such as starch or sugar, caramel, further- more lecithin, or dyestuff(s).
On the dish-ware may a coherent layer of soiling, or - in other embodiments - only one or more spots or limited areas of the respective dish-ware may be soiled. The inventive process is being carried out at temperatures in the range of from 45 to 65°C, preferably 50 to 60°C. Said temperature refers to the temperature of the water being used in the inventive process. The inventive process is being described in more detail below.
The inventive process is being carried out using water. The amount of water is influenced by the type of machine used and by the choice of the program.
Formulations used in the inventive process comprise
(A) in the range of from 1 to 50 % by weight, preferably 10 to 40 % by weight of at least one complexing agent, hereinafter also being referred to as complexing agent (A), said com- plexing agent being selected from the alkali metal salts of citric acid, from the alkali metal salts of aminocarboxylic acids and from sodium tripolyphosphate.
Examples of alkali metal salts in the context of complexing agent (A) are the potassium salts and in particular the sodium salts.
Preferred alkali metal salts of citric acid are the sodium salts, especially the trisodium salt.
Preferred examples of aminocarboxylic acids are methylglycine diacetic acid (MGDA), glutamic acid diacetic acid (GLDA) and iminodisuccinic acid (IDS). Preferred alkali metal salts of aminocarboxylic acids are the trisodium salt of MGDA, the tetrasodium salt of GLDA and the tetra- sodium salt of IDS.
Sodium tripolyphosphate preferably refers to the respective pentasodium salt.
In one embodiment of the present invention, said formulation may contain a combination of at least two complexing agents (A), such as, for example, a combination of alkali metal salts of citric acid and MGDA, or of citric acid and GLDA, or combinations of alkali metal salts of citric acid and sodium tripolyphosphate. Preferred are combinations of the respective sodium salts, in particular combinations of the trisodium salts of citric acid and MGDA. Preferably, formulations used in the inventive process are phosphate-free. In the context of the present invention, the term phosphate-free refers to a combined phosphate and polyphosphate content of 0.01 or less up to 0.5% by weight of phosphate. Formulations used in the inventive process further comprise
(B) in the range of from 2 to 8 % by weight, preferably up to 6 % by weight of at least one non- ionic surfactant of general formula (I) R1-CH(OH)-CH2-0-(AO)x-R2 (I), hereinafter also being referred to as "surfactant (B)", the integers being defined as follows:
R1 is selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C4-C3o-alkyl, straight- chain or branched, more preferred is straight-chain C4-C3o-alkyl and even more preferred is n-Cio-Ci2-alkyl.
R2 is selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C6-C2o-alkyl, more preferred is Cs-Cn-alkyl, x is selected from one to 100, preferably from 5 to 60, more preferably 10 to 50, and even more preferably 20 to 40,
AO is selected from identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (CH2)4-0, CH2CH(CH3)-0, CH(CH3)-CH2-0- and CH2CH(n-C3H7)-0. Preferred example of
Figure imgf000005_0001
In one embodiment of the present invention, (AO)x is selected from (ChbChbOJxi, x1 being selected from one to 50.
In one embodiment of the present invention, (AO)x is selected from
-(CH2CH20)x2-(CH2CH(CH3)-0)x3 and -(CH2CH20)x2-(CH(CH3)CH2-0)x3, x2 and x3 being identi- cal or different and selected from 1 to 30.
In one embodiment of the present invention, (AO)x is selected from -(ChbCI-bO^, x4 = being in the range of from 10 to 50, AO being EO, and R1 and R2 each being independently selected from C8-Ci4-alkyl.
In the context of the present invention, x or x1 or x2 and x3 or x4 are to be understood as average values, the number average being preferred. Therefore, each x or x1 or x2 or x3 or x4 - if applicable - can refer to a fraction although a specific molecule can only carry a whole number of alkylene oxide units.
Formulations used in the inventive process further comprise
(C) in the range of from 0.25 to less than 4 %, preferably 0.5 to 3.5% by weight of a copolymer, hereinafter also being referred to as copolymer (C), being obtained from copolymerizing the following comonomers (a) at least one comonomer, also being referred to as "comonomer (a)", selected from eth- ylenically unsaturated C3-C4-carboxylic acids, for example crotonic acid and preferably (meth)acrylic acid, (E)-crotonic acid, (Z)-crotonic acid, preferred is methacrylic acid and even more preferred is acrylic acid, and from ethylenically unsaturated C4-C8- dicarboxylic acids and their respective anhydrides, for example maleic acid, maleic an- hydride, itaconic acid, itaconic anhydride, citraconic acid, metaconic anhydride and fu- maric acid, preferred is maleic acid and in particular maleic anhydride,
(b) at least one comonomer, also referred to as "comonomer (b)", being selected from isobutene, diisobutene,
C2-C28-a-olefins, preferably from straight-chain C2-C28-a-olefins, for example ethylene, propylene, 1 -butene, 1 -pentene, 1 -hexene, 1 -octene, 1 -decene, 1 -dodecene, 1 - tetradecene, 1 -hexadecene, 1 -octadecene, a-eicosene, and CH2=CH-n-C26H53, pre- ferred are Cio-C28-a-olefins such as, 1 -decene, 1 -dodecene, 1 -tetradecene, 1 - hexadecene, 1 -octadecene, a-eicosene, and CH2=CH-n-C26H53 and mixtures from 1 - hexadecene and 1 -octadecene as well as mixtures from Ci8-C28-a-alkenes, and Ci2-C24-alkyl esters of (meth)acrylic acid, such as (meth)acrylic acid n-Ci2H25-ester, (meth)acrylic acid n-C-uHbsrester, (meth)acrylic acid n-Ci6H33-ester, (meth)acrylic acid n-
CisH37-ester, (meth)acrylic acid n-C2oH4i-ester, (meth)acrylic acid n-C22H45-ester and (meth)acrylic acid n-C24H49-ester.
(c) optionally, at least one further comonomer, also being referred to as "comonomer (c)", such comonomer (c) being selected from non-ionic comonomers and being different from both comonomer (a) and comonomer (b) and not being selected from either group of comonomers (a) and (b).
Percentages of complexing agent (A), surfactant (B) and copolymer (C) are percentages by weight and refer to the total solids content of the respective formulation. In one embodiment of the present invention, copolymer (C) can be obtained by free radical co- polymerization.
In one embodiment of the present invention, comonomer (c) is selected from omethyl styrene, para-methyl styrene and preferably from styrene.
In a preferred embodiment of the present invention, comonomer(s) (c) are selected from the following groups: C4-Cio-alkyl esters of (meth)acrylic acid, such as n-butyl acrylate, n-butyl methacrylate, 2- ethylhexyl acrylate, 2-ethyl hexyl methacrylate, n-hexyl (meth)acrylate, n-octyl (meth)acrylate, and n-decyl (meth)acrylate, vinyl alcohol or allyl alcohol, each alkoxylated with one or more equivalents of C2-C4-alkylene oxide, such as - but not limited to - CH2=CH-0(AO)yH, y being a number in the range of from 1 to 100, in particular CH2=CH-0(CH2CH20)yi H, CH2=CH-0(CH2CH(CH3)0)y2H, y1 and y2 being numbers in the range of from 1 to 100, polyalkylenglycol (meth)acrylates, such as CH2=CH-COO(AO)yH and CH2=C(CH3)COO(AO)yH, alkylen preferably being selected from ethylene, 1 ,2-propylen, 1 ,2-butylen and 1 ,4-butylen, y being a number in the range of from 1 to 100, and (jo-hydroxyalkyl(meth)acrylates, in particular 2-hydroxyethyl(meth)acrylate, polyalkylenglycol monoalkylether (meth)acrylates, preferably polyethylenglycol mono-Ci-C22- alkylether (meth)acrylates, such as CH2=CH-COO(AO)yCH3 and CH2=C(CH3)COO(AO)yCH3, y being a number in the range of from 1 to 100,
AO is being defined as above. In the context of the present invention, y and y1 and y2 are to be understood as average values, the number average being preferred. Therefore, each y or y1 or y2 - if applicable - can refer to a fraction although a specific molecule can only carry a whole number of alkylene oxide units.
In one embodiment of the present invention, copolymer (C) has an average molecular weight Mw in the range of from 1 ,000 to 30,000 g/mol, preferably 2,000 to 10,000 g/mol, determined, for example, by gel permeation chromatography (GPC) or size exclusion chromatography, and referring to the acid/salt.
In one embodiment of the present invention, copolymer (C) exhibits a polydispersity Mw/Mn in the range of from 1 .5 to 10, preferably 2 to 5. In a preferred embodiment of the present invention, copolymer (C) is used as its alkali metal salt, its carboxyl groups being partially or preferably fully neutralized with alkali, preferably with sodium. In one embodiment of the present invention, copolymer (C) is selected from random copolymers, alternating copolymers, block copolymers and multiblock copolymers.
In one embodiment of the present invention, comonomer (a) is selected from maleic acid and maleic anhydride and comonomer (b) is selected from isobutene, diisobutene and C2-C28-0 olefins, preferably from straight-chain C2-C28-a-olefins. Such copolymers (C) are preferably alternating copolymers.
In another embodiment of the present invention, comonomer (a) is selected from (meth)acrylic acid and comonomer (b) is selected from Ci2-C24-alkyl esters of (meth)acrylic acid. Such copol- ymers (C) are preferably random copolymers.
In one embodiment of the present invention, copolymer (C) is made from
40 to 80 % by weight of one or more comonomer(s) (a),
10 to 60 % by weight of one or more comonomer(s) (b) selected from isobutene, diisobutene, and C2-C28-a-olefins, and, optionally
up to 20 % by weight of comonomer (c).
In another embodiment of the present invention, copolymer (C) is made from
50 to 95 % by weight of one or more comonomer(s) (a),
5 to 25 % by weight of one or more comonomer(s) (b) selected from Ci2-C24-alkyl esters of (meth)acrylic acid, and, optionally
up to 20 % by weight of comonomer (c).
Percentages are referring to the total respective copolymer (C) as free acid.
In one embodiment of the present invention, formulations used in the inventive process may have a total solids content in the range of from 90 to 99.9%, preferably 95 to 99 % by weight. Such inventive formulations are, e. g., in the form of powder or tablets. In one embodiment of the present invention, formulations used in the inventive process may have a total solids content in the range of from 15 to 40% by weight. Such inventive formulations are, e. g., in the form of gels.
In one embodiment of the present invention, the inventive process comprises several steps, one of the steps being contacting the soiled dishware with a formulation as disclosed above, and also comprising at least one rinsing step and at least one drying step. Preferably, the formulation used in the inventive process can be used as 2-in-1 or 3-in-1 formulation, and no separate rinse agent is necessary. In another preferred embodiment, the ion exchange does not need to be treated with regenerating salt. Even more preferably, the formulation used in the inventive process can be used as 2-in-1 or 3-in-1 formulation, and neither a separate rinse agent nor a regenerating salt is necessary.
In one embodiment of the present invention, formulations used in the inventive process may contain at least one further ingredient, also being referred to as ingredient (D). Ingredient (D) may be selected from one or more surfactants other than surfactant (B), one or more enzymes, one or more builders other than complexing agent (A), in particular phosphorus-free builders, one or more cobuilders, one or more alkali carriers, one or more bleaching agents, one or more bleach catalysts, one or more bleach activators, one or more bleach stabilizers, one or more antifoams, one or more corrosion inhibitors, one or more buffer or one or more dyes.
Examples of surfactants other than surfactant (B) are in particular nonionic surfactants other than surfactant (B) as well as mixtures of anionic or zwitterionic surfactants with nonionic surfactants other than surfactant (B). Preferred nonionic surfactants other than surfactant (B) are alkoxylated alcohols and alkoxylated fatty alcohols, di- and multiblock copolymers of ethylene oxide and propylene oxide and reaction products of sorbitan with ethylene oxide or propylene oxide, alkyl glycosides and so-called amine oxides.
Preferred examples of alkoxylated alcohols and alkoxylated fatty alcohols are, for example, compounds of the general formula (II)
Figure imgf000009_0001
in which the variables are defined as follows: is selected from hydrogen and from Ci-Cio-alkyl, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, sec-pentyl, neopentyl, 1 ,2- dimethylpropyl, isoamyl, n-hexyl, isohexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n- nonyl, n-decyl or isodecyl, is identical or different and selected from linear Ci-Cio-alkyl, preferably in each case identical and ethyl and particularly preferably methyl,
R5 is selected from Cs-C22-alkyl, for example n-CsH , n-doHb-i , n-Ci2H25, n-C-uHbsi, n-Ci6H33
m and n are in the range from zero to 300, where the sum of n and m is at least one. Preferably, m is in the range from 1 to 100 and n is in the range from 0 to 30. Compounds of the general formula (II) may be block copolymers or random copolymers, preference being given to block copolymers.
Other preferred examples of alkoxylated alcohols and alkoxylated fatty alcohols are, for exam- pie, compounds of the general formula (III)
Figure imgf000010_0001
in which the variables are defined as follows: is identical or different and selected from linear Ci-C4-alkyl, preferably identical case and ethyl and particularly preferably methyl,
R6 is selected from C6-C2o-alkyl, in particular n-CsH , n-doHb-i , n-Ci2H25, n-C-uFbs), n-Ci6H33,
a is a number in the range from 1 to 6, b is a number in the range from 4 to 20, d is a number in the range from 4 to 25.
Compounds of the general formula (III) may be block copolymers or random copolymers, preference being given to block copolymers.
Further suitable nonionic surfactants are selected from di- and multiblock copolymers, composed of ethylene oxide and propylene oxide. Further suitable nonionic surfactants are selected from ethoxylated or propoxylated sorbitan esters. Amine oxides or alkyl glycosides are likewise suitable. An overview of suitable further nonionic surfactants can be found in EP-A 0 851 023 and in DE-A 198 19 187.
Mixtures of two or more different nonionic surfactants other than surfactant (B) may also be present.
Examples of anionic surfactants are Cs-C2o-alkyl sulfates, C8-C20-alkylsulfonat.es and C8-C20- alkyl ether sulfates with one to 6 ethylene oxide units per molecule.
In one embodiment of the present invention, formulations used in the inventive process can comprise in the range from 3 to 20% by weight of surfactant other than surfactant (B). Formulations used in the inventive process can comprise one or more enzymes. Examples of enzymes are lipases, hydrolases, amylases, proteases, cellulases, esterases, pectinases, lactases and peroxidases. Formulations used in the inventive process can comprise, for example, up to 5% by weight of enzyme, preference being given to 0.1 to 3% by weight, in each case based on the total solids content of the formulation according to the invention.
Over and above complexing agent (A), formulations used according to the invention can com- prise one or more builders, in particular phosphate-free builders. Examples of suitable builders are fatty acid sulfonates, ohydroxypropionic acid, alkali metal malonates, fatty acid sulfonates, alkyl and alkenyl disuccinates, tartaric acid diacetate, tartaric acid monoacetate, oxidized starch, and polymeric builders, for example polycarboxylates and polyaspartic acid. In one embodiment of the present invention, builders are selected from polycarboxylates, for example alkali metal salts of (meth)acrylic acid homopolymers or (meth)acrylic acid copolymers.
Suitable comonomers of polycarboxylates are monoethylenically unsaturated dicarboxylic acids such as maleic acid, fumaric acid, maleic anhydride, itaconic acid and citraconic acid.
A suitable (meth)acrylic acid homopolymer is in particular polyacrylic acid, which preferably has an average molecular weight Mw in the range from 2,000 to 40,000 g/mol, preferably 2,000 to 10,000 g/mol, in particular 3,000 to 8,000 g/mol. Also of suitability are copolymeric polycarboxylates, in particular those of acrylic acid with methacrylic acid and of acrylic acid or methacrylic acid with maleic acid and/or fumaric acid.
Formulations used according to the invention can comprise, for example, in the range from in total 2.5 to 20% by weight, preferably up to 10% by weight, of builders other than complexing agent (A).
In one embodiment of the present invention, formulations used according to the invention can comprise one or more cobuilders.
Examples of cobuilders are phosphonates, for example hydroxyalkanephosphonates and ami- noalkanephosphonates. Among the hydroxyalkanephosphonates, 1 -hydroxyethane-1 ,1 - diphosphonate (HEDP) is of particular importance as a cobuilder. It is preferably used as the sodium salt, the disodium salt giving a neutral reaction and the tetrasodium salt an alkaline reaction (pH 9). Suitable aminoalkanephosphonates are preferably ethylenediaminetetra- methylenephosphonate (EDTMP), diethylenetriaminepentamethylenephosphonate (DTPMP) and higher homologs thereof. They are preferably used in the form of the neutrally reacting sodium salts, e.g. as hexasodium salt of EDTMP or as hepta- and octasodium salt of DTPMP. Moreover, amphoteric polymers can also be used as cobuilders.
Formulations used in the inventive process can comprise one or more alkali carriers. Alkali carriers ensure, for example, a pH of at least 9 if an alkaline pH is desired. Of suitability are, for example, alkali metal carbonates, alkali metal hydrogen carbonates, alkali metal hydroxides and alkali metal metasilicates. A preferred alkali metal is in each case potassium, particular preference being given to sodium.
Formulations used in the inventive process can comprise one or more bleach catalysts. Bleach catalysts can be selected from bleach-boosting transition metal salts or transition metal complexes such as, for example, manganese-, iron-, cobalt-, ruthenium- or molybdenum-salen complexes or carbonyl complexes. Manganese, iron, cobalt, ruthenium, molybdenum, titanium, vanadium and copper complexes with nitrogen-containing tripod ligands and also cobalt-, iron-, copper- and ruthenium-amine complexes can also be used as bleach catalysts.
Formulations used in the inventive process can comprise, for example, 0.5 to 15% by weight of bleaching agents, hereinafter also referred to as bleach (D). Bleach (D) can be selected from oxygen bleaches and chlorine-containing bleaches. Examples of suitable oxygen bleaches are sodium perborate, anhydrous or for example as monohydrate or as tetrahydrate or so-called dihydrate, sodium percarbonate, anhydrous or, for example, as monohydrate, hydrogen peroxide, persulfates, organic peracids such as peroxylauric acid, peroxystearic acid, peroxy-a-naphthoic acid, 1 ,12-diperoxydodecanedioic acid, per- benzoic acid, peroxylauric acid, 1 ,9-diperoxyazelaic acid, diperoxyisophthalic acid, in each case as free acid or as alkali metal salt, in particular as sodium salt, also sulfonylperoxy acids and cationic peroxy acids.
Formulations used in the inventive process can comprise, for example, in the range from 0.5 to 15% by weight of oxygen bleach.
Suitable chlorine-containing bleaches are, for example, 1 ,3-dichloro-5,5-dimethylhydantoin, N- N-chlorosulfamide, chloramine T, chloramine B, sodium hypochlorite, calcium hypochlorite, magnesium hypochlorite, potassium hypochlorite, potassium dichloroisocyanurate and sodium dichloroisocyanurate.
Formulations used in the inventive process can preferably comprise, for example, in the range from 3 to 10% by weight of chlorine-containing bleach.
Formulations used in the inventive process can comprise one or more bleach activators, for example N-methylmorpholinium-acetonitrile salts ("MMA salts"), trimethylammonium acetonitrile salts, N-acylimides such as, for example, N-nonanoylsuccinimide, 1 ,5-diacetyl-2,2- dioxohexahydro-1 ,3,5-triazine ("DADHT") or nitrile quats (trimethylammonium acetonitrile salts). Other examples of suitable bleach activators are tetraacetylethylenediamine (TAED) and tetraacetylhexylenediamine.
Formulations used in the inventive process can comprise one or more corrosion inhibitors. In the present case, this is to be understood as including those compounds which inhibit the corrosion of metal. Examples of suitable corrosion inhibitors are triazoles, in particular benzotria- zoles, bisbenzotriazoles, aminotriazoles, alkylaminotriazoles, also phenol derivatives such as, for example, hydroquinone, pyrocatechol, hydroxyhydroquinone, gallic acid, phloroglucinol or pyrogallol.
In one embodiment of the present invention, formulations used in the inventive process comprise in total in the range from 0.1 to 1.5% by weight of corrosion inhibitor.
Formulations used in the inventive process can comprise one or more fillers, for example sodi- urn sulfate.
Formulations used in the inventive process can comprise one or more antifoams, selected for example from silicone oils and paraffin oils. In one embodiment of the present invention, formulations used in the inventive process comprise in total in the range from 0.05 to 0.5% by weight of antifoam.
Dishware cleaned according to the inventive process exhibits excellent properties, such as very good removal of soiling, especially of fat. Furthermore, dishware cleaned according to the in- ventive process show excellent values for spotting, filming and residues. In addition, when modern dishwashing machines are used, the filter(s) and/or sieves will contain only very low amounts of surfactant and fat after operation.
A further aspect of the present invention are formulations, hereinafter also being referred to as inventive formulations, with whom the inventive process can advantageously be carried out. Inventive formulations may be unit doses, such as tablets, or as gel or powder, as granules or compactate. In a preferred embodiment, such a unit dose comprises 10 to 30 g of inventive formulation. Inventive formulations may be solid, and in such embodiments they may contain some residual humidity, such as 0.01 to 10 % by weight, water. In other embodiments, inventive formulations may be liquids or gels.
Inventive formulations comprise
(A) in the range of from 1 to 50 % by weight, preferably 10 to 40 % by weight of at least one complexing agent (A), said complexing agent being selected from the alkali metal salts of citric acid, from the alkali metal salts of aminocarboxylic acids and from sodium tripolyphosphate.
Examples of alkali metal salts in the context of complexing agent (A) are the potassium salts and in particular the sodium salts.
Preferred alkali metal salts of citric acid are the sodium salts, especially the trisodium salt.
Preferred examples of aminocarboxylic acids are methylglycine diacetic acid (MGDA), glutamic acid diacetic acid (GLDA) and iminodisuccinic acid (IDS). Preferred alkali metal salts of aminocarboxylic acids are the trisodium salt of MGDA, the tetrasodium salt of GLDA and the tetra- sodium salt of IDS.
Sodium tripolyphosphate preferably refers to the respective pentasodium salt.
In one embodiment of the present invention, inventive formulations may contain a combination of at least two complexing agents (A), such as, for example, a combination of alkali metal salts of citric acid and MGDA, or of citric acid and GLDA, or combinations of alkali metal salts of citric acid and sodium tripolyphosphate. Preferred are combinations of the respective sodium salts, in particular combinations of the trisodium salts of citric acid and MGDA.
Preferably, inventive formulations are phosphate-free. In the context of the present invention, the term phosphate-free refers to a combined phosphate and polyphosphate content of 0.01 or less up to 0.5% by weight of phosphate.
Inventive formulations further comprise
(B) in the range of from 2 to 8 % by weight, preferably 3 to 6 % by weight of surfactant (B)
R -CH(OH)-CH2-0-(AO)x-R2 (I), the integers being defined as follows:
R1 is selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C4-C3o-alkyl, straight- chain or branched, more preferred is straight-chain C4-C3o-alkyl and even more preferred is n-Cio-Ci2-alkyl. is selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C3o-alkenyl, straight- chain or branched, with at least one C-C double bond, preferred is C6-C2o-alkyl, more preferred is Cs-Cn-alkyl. x is selected from one to 100, preferably from 5 to 60, more preferably 10 to 50, and even more preferably 20 to 40,
AO is selected from identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (CH2)4-0, CH2CH(CH3)-0, CH(CH3)-CH2-0- and CH2CH(n-C3H7)-0. Preferred example of
Figure imgf000015_0001
In one embodiment of the present invention, (AO)x is selected from
Figure imgf000015_0002
, x1 being selected from one to 50.
In one embodiment of the present invention, (AO)x is selected from -(ChbCI-bO^- (CH2CH(CH3)-0)x3, x2 and x3 being identical or different and selected from 1 to 30.
In one embodiment of the present invention, (AO)x is selected from -(ChbCI-bO^, x4 = being in the range of from 10 to 50, AO being EO, and R1 and R2 each being independently selected from C8-Ci4-alkyl.
Inventive formulations further comprise (C) in the range of from 0.25 to less than 4 %, preferably 0.5 to 3.5% by weight of copolymer (C), being obtained from copolymerizing the following comonomers
(a) at least one comonomer (a), selected from ethylenically unsaturated C3-C4-carboxylic acids, for example crotonic acid and preferably (meth)acrylic acid, (E)-crotonic acid, (Z)- crotonic acid, preferred is methacrylic acid and even more preferred is acrylic acid, and from ethylenically unsaturated C4-C8-dicarboxylic acids and their respective anhydrides, for example maleic acid, maleic anhydride, itaconic acid, itaconic anhydride, citraconic acid, metaconic anhydride and fumaric acid, preferred is maleic acid and in particular maleic anhydride,
(b) at least one comonomer (b), being selected from isobutene, diisobutene, C2-C28-a-olefins, preferably from straight-chain C2-C28-a-olefins, for example ethylene, propylene, 1 -butene, 1 -pentene, 1 -hexene, 1 -octene, 1 -decene, 1 -dodecene, 1 - tetradecene, 1 -hexadecene, 1 -octadecene, and a-eicosene, preferred are Cio-C2o-a- olefins such as, 1 -decene, 1 -dodecene, 1 -tetradecene, 1 -hexadecene, 1 -octadecene, and mixtures from 1 -hexadecene and 1 -octadecene, and Ci2-C24-alkyl esters of (meth)acrylic acid, such as (meth)acrylic acid n-Ci2H25-ester, (meth)acrylic acid n-Ci4H29-ester, (meth)acrylic acid n-Ci6H33-ester, (meth)acrylic acid n- CisH37-ester, (meth)acrylic acid n-C2oH4i-ester, and (meth)acrylic acid n-C24H49-ester. (c) optionally, at least one comonomer (c) selected from non-ionic comonomers, such
comonomer (c) being different from both comonomer (a) and comonomer (b) and not being selected from either group of comonomers (a) and (b).
Percentages of complexing agent (A), surfactant (B) and copolymer (C) are percentages by weight and refer to the total solids content of the respective formulation.
Comonomers (a), (b) and (c) have been defined above.
Preferably, inventive formulations are phosphate-free.
In one embodiment of the present invention, copolymer (C) has an average molecular weight Mw in the range of from 1 ,000 to 30,000 g/mol, preferably up to 10,000 g/mol, determined by GPC. In one embodiment of the present invention, copolymer (C) exhibits a polydispersity Mw/Mn in the range of from 1.5 to 10, preferably 2 to 5.
In a preferred embodiment of the present invention, copolymer (C) is used as its alkali metal salt, its carboxyl groups being partially or preferably fully neutralized with alkali, preferably with sodium.
In one embodiment of the present invention, copolymer (C) is selected from random copolymers, alternating copolymers, block copolymers and multiblock copolymers. In one embodiment of the present invention, comonomer (a) is selected from maleic acid and maleic anhydride and comonomer (b) is selected from isobutene, diisobutene and C2-C28-0 olefins, preferably from straight-chain C2-C28-a-olefins. Such copolymers (C) are preferably alternating copolymers.
In another embodiment of the present invention, comonomer (a) is selected from (meth)acrylic acid and comonomer (b) is selected from Ci2-C24-alkyl esters of (meth)acrylic acid. Such copolymers (C) are preferably random copolymers.
In one embodiment of the present invention, inventive formulations have a total solids content in the range of from 90 to 99.9%, preferably 95 to 99 % by weight. Such inventive formulations are, e. g., in the form of powder or tablets. In one embodiment of the present invention, inventive formulations have a total solids content in the range of from 15 to 40% by weight. Such inventive formulations are, e. g., in the form of gels. In one embodiment of the present invention, inventive formulations may contain at least one further ingredient, also being referred to as ingredient (D). Ingredient (D) may be selected from one or more surfactants other than surfactant (B), one or more enzymes, one or more builders other than complexing agent (A), in particular phosphorus-free builders, one or more cobuilders, one or more alkali carriers, one or more bleaching agents, one or more bleach catalysts, one or more bleach activators, one or more bleach stabilizers, one or more antifoams, one or more corrosion inhibitors, one or more buffer or one or more dyes. Ingredients (D) have been explained in more detail above.
Inventive formulations are excellently suitable for carrying out the inventive process.
A further aspect of the present invention is a process for making inventive formulations, hereinafter also being referred to as inventive manufacturing process. The inventive manufacturing process comprises mixing complexing agent (A), surfactant (B) and copolymer (C) and, if applicable, one or more further ingredient (D), in one or more steps. Such mixing can be performed in the absence or presence of water, preferably mixing is being performed in the absence of water. In other embodiments, at least one of the components complexing agent (A), surfactant (B) and copolymer (C) or, if applicable, one or more further ingredient (D), is added as aqueous solution to other components that are powdery or in the form of granules, and the water is being removed during or after mixing. Mixing can be performed at a temperature in the range of from 5 to 100°C, preferably 20 to 70°C or at ambient temperature.
In one embodiment of the present invention, the inventive manufacturing process is being carried out in the presence of water, and such water is at least partially removed at the end of the inventive manufacturing process, for example by spray-drying or by making compactates of granules of different components or of premixed components.
The invention is further explained by the following working examples. The following ingredients were used:
(A.1 ): trisodium salt of methyl glycine diacetic acid
(A.2): trisodium salt of citric acid
Surfactant (B.1 ): n-C8Hi7-CH(OH)-CH2-0-(EO)22-CH(CH3)-CH2-0-n-CioH2i
Surfactant (B.2): n-CioH2i-CH(OH)-CH2-0-(EO)4o-n-CioH2i Copolymer (C.1 ): fully neutralized sodium salt of random copolymer from maleic acid anhydride (a.1 ), CH2=CH-n-Ci6H33 (b.1 )/isobutene (b.2); 65 % by weight of (a.1 ), 9 % by weight of (b.1 ), 26 % by weight of (b.2), percentages referring to the respective free acid of (C.1 ) Synthesis of copolymer (C.1 ):
O-Xylene (363 g) and maleic acid anhydride (a.1 ) (196 g) were placed in an autoclave equipped with metering and distillation devices and a stirrer. The autoclave was purged with 3 bar of nitrogen three times. The pressure was then reduced to 91 mbar and the mixture of (a.1 ) and o- xylene was heated to 120°C. The following feeds were added simultaneously at 120°C, each with constant rate , starting at the same time:
25.2 g CH2=CH-n-Ci6H33 (b.1 ) over a period of 3 hours,
78.4 g of isobutene (b.2) over a period of 5 hours and tert-butylperoxy-2-ethylhexanoate (8.31 g) dissolved in 35 g o-xylene over a period of 5.5 hours. When the addition of tert-butylperoxy-2- ethylhexanoate had been completed, the reaction mixture was further stirred for 1 hour at 120°C. The pressure in the autoclave was then released to atmospheric pressure. The reaction mixture was cooled to 100°C and then diluted with 310 ml of water. O-Xylene was then removed by steam distillation. The mixture so obtained was neutralized by addition of 205 ml 50 wt% aqueous sodium hydroxide solution within 2 hours and then cooled to room temperature to yield a clear solution with a solid content of 40 wt%. Average molecular weight Mw: 4330 g/mol, as sodium salt, partially neutralized (pH value: 7)
Copolymer (C.2): fully neutralized sodium salt of random copolymer from acrylic acid
(a.2)/methacrylic acid stearyl ester (b.3), 90 % by weight of (a.2), 10% by weight of (b.3), percentages referring to the respective free acid
Synthesis of copolymer (C.2):
A polymerization vessel equipped with an anchor stirrer and metering devices was charged with a solution of 5 g od acrylic acid (a.2) in 175 g of isopropanol. The mixture was heated to 80°C under an atmosphere of nitrogen. The following feeds were added simultaneously at 80°C, each with constant rate, starting at the same time:
a solution of 175 g of acrylic acid (a.2) in 200 g of isopropanol, over a period of 6 hours, a solution of 20 g of methacrylic acid stearyl ester (b.3) in 200 g of isopropanol over a period 5.5 hours, and
9.5 g tert-butyl perpivalate, dissolved in 50 g of isopropanol within 6.5 hours. When the addition of the tert-butyl perpivalate had been completed, the resulting reaction mixture was further stirred at 80°C for 1 hour, and another 2.7 g of tert-butylperoxypivalate, dissolved in 10 g of isopropanol, were added. Then the reaction mixture so obtained was further stirred for 1 hour at 80°C. Isopropanol was removed by means of steam distillation. The pH value of aqueous mix- ture so obtained was adjusted to 7.0 with aqueous sodium hydroxide solution to yield a clear aqueous polymer solution with a solid content of 23.2 wt.%. Mw: 5180 g/mol. The weight-average molecular weight (Mw) of copolymer (C.2) was determined by GPC (gel permeation chromatography) at 23 °C, using a PSS Suprema column (PSS, Mainz, Germany). The eluent employed was an aqueous tris(hydroxymethyl)amino methane (TRIS) buffer solution (0.02 M), containing 0.2 M sodium chloride. A differential refractometer was used for detection. Calibration was carried out using dextran/pullulan standards.
(D.3): Polyacrylic acid Mw 4000 g/mol, as sodium salt, completely neutralized
The following base detergent composition was used:
Table 1 : Base mixtures for experiments with formulations according to the invention and comparison formulations
Figure imgf000019_0001
All data in g. Firstly, base mixtures were prepared from the feed materials according to table 1. The feed materials as well as copolymer (C.1 ), copolymer (C.2) and/or polymer (D.3) were mixed in dry state apart from (B.1 ) and (B.2), which were finally added in molten form.
General remarks about the dish-wash process:
Rinsing experiments:
All dish-wash experiments were carried out in Miele automatic dish wash machines, type G1222 SCL. The program 50°C ("R-time 2", for washing) and 65° for rinsing was selected. No separate rinsing agent was added, no regenerating salt was used. The dish-wash experiments were car- ried out with water, 21 ° dH (German hardness), Ca/Mg:HC03 (3:1 ):1.35. In each experiment three knives (stainless steel), three blue melamine resin plates, three drinking glasses and three plates from china were placed in the dishwasher. Before each cycle 100 g of soil, comprising fat, protein and starch in the form of margarine, egg-yolk and starch, were added. In each cycle, Between two cycles, a waiting period of one hour was left, of which 10 minutes were with the door of the dishwashing machine closed and 50 minutes with open door. The dishes were checked by visual assessment of the ware after 6 cycles in a darkened chamber under light behind an aperture diaphragm was awarded using a grading scale from 1 (very poor) to 10 (very good). In addition, the sieves of the machines were checked by visual assessment and rated using average grades from 1 (high amounts of greasy residues) to 5 (clean sieve).
Base mixture according to table 1 , (D.3) and copolymer (C.1 ) were mixed according to table 2 and tested. The results are summarized in table 2.
Table 2: Rinsing Test
Figure imgf000020_0001
"Sieves (grade)" refers to an average grade. The sieves and filters only contained very little fat and detergent when TF.2 was used. When C-TF.1 was used, soiling of the sieve could be ob- served after the 6th cycle.
Residue removal experiments:
All dish-wash experiments were carried out in Miele automatic dish wash machines, type G1222 SCL. The program 65°C for washing and rinsing was selected. No separate rinsing agent was added, no regenerating salt was used. The dish-wash experiments were carried out with water, 21 ° dH (German hardness), Ca/Mg:HC03 (3:1 ):1.35. In each experiment three knives (stainless steel), three blue melamine resin plates, three drinking glasses and three plates from china were placed in the dishwasher. Together with the detergent 50 g of the ballast soil according to table 4 was added into the dish wash machine. In each cycle, 18 g of a formulation according to tables 1 and 3 was added.
Between two cycles, a waiting period of one hour was left, of which 10 minutes were with the door of the dishwashing machine closed and 50 minutes with open door. The dishes were checked by visual assessment of the ware after 30 cycles in a darkened chamber under light behind an aperture diaphragm was awarded using a grading scale from 1 (very poor) to 10 (very good). In addition, the sieves of the machines were checked by visual assessment and rated using average grades from 1 (high amounts of greasy residues) to 5 (clean sieve). Table 3: Residue Tests
Figure imgf000021_0001
"Sieves (grade)" refers to an average grade. The sieves and filters only contained very little fat and detergent when TF.4 or TF.5 was used. When C-TF.3 was used, strong soiling of the sieve could be observed after the 30th cycle.
When copolymer (C.2) was used instead of copolymer (C.1 ) the same trend was observed.
Table 4: Composition of soil for rinsing experiments
Soil component % by weight
Starch Potato starch 0.5
Gravy 2.5
Oil /grease margarine 10.2
Protein Egg yolk 5.1
Reduced fat milk 5.1
Others Tomato ketchup 2.5
Mustard 2.5
Benzoic acid 0.1
Demineralized water 71.5
Sum 100

Claims

Patent claims
Process for cleaning dishware soiled with fatty residue, characterized in that said process is carried out at a temperature in the range of from 45 to 65°C and using at least one formulation, comprising
(A) in the range of from 1 to 50 % by weight of at least one complexing agent, selected from the alkali metal salts of citric acid, of aminocarboxylic acids and from sodium tripolyphosphate,
(B) in the range of from 2 to 8 % by weight of at least one non-ionic surfactant of general formula (I)
R -CH(OH)-CH2-0-(AO)x-R2 (I)
(C) in the range of from 0.25 to less than 4 % by weight of a copolymer, being obtained from copolymerizing the following comonomers
(a) at least one comonomer selected from ethylenically unsaturated C3-C4-carboxylic acids and ethylenically unsaturated C4-C8-dicarboxylic acids or their respective anhydrides,
(b) at least one comonomer selected from isobutene, diisobutene, C2-C28-a-olefins, and Ci2-C24-alkyl esters of (meth)acrylic acid,
(c) optionally, at least one further comonomer selected from non-ionic comonomers, the integers being defined as follows:
R1 being selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C30- alkenyl, straight-chain or branched, with at least one C-C double bond,
R2 being selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C30- alkenyl, straight-chain or branched, with at least one C-C double bond, x being selected from one to 100,
AO being identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (CH2)4-0, CH2CH(CH3)-0, CH(CH3)-CH2-0- and CH2CH(n-C3H7)-0, percentages being based on the total solids content of said formulation.
Process according to claim 1 , wherein said formulation contains 10 to 40 % by weight complexing agent (A). Process according to claim 1 or 2, wherein complexing agent (A) is selected from the alkali metal salts of methyl glycine diacetate (MGDA), imino succinic acid (IDS) and glutamic acid diacetate (GLDA).
Process according to any of claims 1 to 3, wherein copolymer (C) has an average molecular weight Mw in the range of from 1 ,000 to 30,000 g/mol.
Process according to any of claims 1 to 4, wherein further comonomer(s) (c) are selected from C4-Cio-alkyl esters of (meth)acrylic acid, , polyalkylenglycol (meth)acrylates, poly- alkylenglycol monoalkylether (meth)acrylates , ω-hydroxyalkyl(meth)acrylates, and vinyl alcohol or allyl alcolhol, each alkoxylated with one or more equivalents of C2-C4-alkylene oxide.
Process according to any of claims 1 to 5, wherein said formulation further contains the alkali metal salt of a (meth)acrylic acid homopolymer.
Process according to any of claims 1 to 6, wherein copolymer (C) is selected from alternating copolymers in which comonomer (a) is selected from maleic acid and maleic anhydride.
Formulation, comprising
(A) in the range of from 1 to 50 % by weight of at least one complexing agent, selected from the alkali metal salts of citric acid, aminocarboxylic acids, and from sodium tripolyphosphate,
(B) in the range of from 2 to 8 % by weight of at least one non-ionic surfactant of general formula (I)
R -CH(OH)-CH2-0-(AO)x-R2 (I)
(C) in the range of from 0.25 to less than 4 % by weight of a copolymer, being obtained from copolymerizing the following comonomers
(a) at least one comonomer selected from ethylenically unsaturated C3-C4-carboxylic acids and ethylenically unsaturated C4-C8-dicarboxylic acids or their respective anhydrides,
(b) at least one comonomer selected from isobutene, diisobutene, C2-C28-a-olefins, and Ci2-C24-alkyl esters of (meth)acrylic acid,
(c) optionally, at least one further comonomer selected from non-ionic comonomers, the integers being defined as follows:
R1 being selected from C4-C3o-alkyl, straight-chain or branched, and from C4-C30- alkenyl, straight-chain or branched, with at least one C-C double bond, R2 being selected from Ci-C3o-alkyl, straight-chain or branched, and from C2-C30- alkenyl, straight-chain or branched, with at least one C-C double bond, x being selected from one to 100,
AO being identical or different alkylene oxides, selected from CH2-CH2-O, (CH2)3-0, (CH2)4-0, CH2CH(CH3)-0, CH(CH3)-CH2-0- and CH2CH(n-C3H7)-0, percentages being based on the total solids content of said formulation.
9. Formulation according to claim 8, wherein said formulation contains 10 to 40 % by weight complexing agent (A).
10. Formulation according to claim 8 or 9, wherein complexing agent (A) is selected from the alkali metal salts of methyl glycine diacetate (MGDA), imino succinic acid (IDS) and glutamic acid diacetate (GLDA).
1 1 . Formulation according to any of claims 8 to 10, wherein further comonomer(s) (c) are selected from C4-Cio-alkyl esters of (meth)acrylic acid, polyalkylenglycol (meth)acrylates, polyalkylenglycol monoalkylether (meth)acrylates, (jO-hydroxyalkyl(meth)acrylates, and vinyl alcohol or allyl alcohol, each alkoxylated with one or more equivalents of C2-C4- alkylene oxide.
12. Formulation according to any of claims 8 to 1 1 , wherein said formulation further contains the alkali metal salt of a (meth)acrylic acid homopolymer.
13. Formulation according to any of claims 8 to 12, wherein copolymer (C) has an average molecular weight Mw in the range of from 1 ,000 to 30,000 g/mol. 14. Formulation according to any of claims 8 to 13, wherein copolymer (C) is an alternating copolymer.
15. Formulation according to any of claims 8 to 14, wherein copolymer (C) is selected from alternating copolymers in which comonomer (a) is selected from maleic acid and maleic anhydride.
PCT/EP2014/063279 2013-07-04 2014-06-24 Process for cleaning dishware WO2015000744A1 (en)

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RU2016103485A RU2016103485A (en) 2013-07-04 2014-06-24 COOKWARE CLEANING METHOD
EP14731978.4A EP3017030A1 (en) 2013-07-04 2014-06-24 Process for cleaning dishware
US14/902,776 US9938489B2 (en) 2013-07-04 2014-06-24 Process for cleaning dishware
KR1020167003198A KR20160030256A (en) 2013-07-04 2014-06-24 Process for cleaning dishware
CN201480037687.4A CN105358669A (en) 2013-07-04 2014-06-24 Process for cleaning dishware
JP2016522443A JP2016530348A (en) 2013-07-04 2014-06-24 How to wash dishes

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