CA2236881C - A peracid based dishwashing detergent composition - Google Patents
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Abstract
A warewashing composition for a machine dishwasher and a method of using it is described. The composition comprises effective amounts of an organic peroxy acid, and an amylase enzyme which, when incubat ed at 55 .degree.C in a solution of 2mM sodium citrate, 1mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half - life of two minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405nm of solution samples incubated with p-nitrophenyl-.alpha.-D-maltoheptaoside as substrate and gluco amylase and .alpha.-glucosidase as coupled enzymes; and 1 % to 75 % by weight of a builder. A 1 % aqueous solution of the composition must have a pH of less than 10.
Description
z A PERACID BASED DISH~PASIiING DETERGENT COMPOSITION
Field of the Invention The invention relates to a low alkalinity dishwashing detergent composition containing a peracid, a bleach resistant amylase and a builder. A method of using the composition is also described.
Baokqrouad of the Invention Many conventional dishwashing systems use high alkalinity cleaning compositions which may include chlorine bleach as sanitizer. Whilst these systems are highly effective with regard to the removal of hydrophilic and bleachable stains from dishware, they have an inherent weakness with respect to the removal of starch-containing food soils. Incomplete removal of starch in successive washes leads to a gradual build-up of soil so that after only one to two weeks of cleaning with these systems the appearance of the dishware can become unacceptable. At this point, extensive soaking of the dishware may be required which is a separate operation that is laborious, time-consuming, and very expensive. Such build up problems are especially pronounced in industrial and institutional warewashing where foods and dishware are subject to high temperatures for prolonged periods of time during food preparation, distribution and serving.
Amylase enzymes have been proposed as a solution to the problem of starch build-up on cleaned dishware. However, ' 30 amylases are less effective at wash pHs greater than 10 (see GB-A-1 296 839 (Novo)), and are incompatible with chlorine bleach. As a consequence, trends in formulating dishwashing compositions with amylase have been toward the use of peroxygen bleaching agents in lieu of halogen bleach sources.
Field of the Invention The invention relates to a low alkalinity dishwashing detergent composition containing a peracid, a bleach resistant amylase and a builder. A method of using the composition is also described.
Baokqrouad of the Invention Many conventional dishwashing systems use high alkalinity cleaning compositions which may include chlorine bleach as sanitizer. Whilst these systems are highly effective with regard to the removal of hydrophilic and bleachable stains from dishware, they have an inherent weakness with respect to the removal of starch-containing food soils. Incomplete removal of starch in successive washes leads to a gradual build-up of soil so that after only one to two weeks of cleaning with these systems the appearance of the dishware can become unacceptable. At this point, extensive soaking of the dishware may be required which is a separate operation that is laborious, time-consuming, and very expensive. Such build up problems are especially pronounced in industrial and institutional warewashing where foods and dishware are subject to high temperatures for prolonged periods of time during food preparation, distribution and serving.
Amylase enzymes have been proposed as a solution to the problem of starch build-up on cleaned dishware. However, ' 30 amylases are less effective at wash pHs greater than 10 (see GB-A-1 296 839 (Novo)), and are incompatible with chlorine bleach. As a consequence, trends in formulating dishwashing compositions with amylase have been toward the use of peroxygen bleaching agents in lieu of halogen bleach sources.
Because oxygen bleaching systems tend to be less effective than chlorine on tannin stains, those cleaning systems that use amylase enzymes and which have been proposed to date, provide only moderate levels of removal of bleachable stains such as tannin. Indeed, no single system that has been proposed to date can effectively meet the requirements of excellent starch and tannin removal.
Bleach resistant amylase enzymes described in the art may be incorporated with either halogen or peroxygen bleaches in a detergent composition, as described in WO-94/02597 {Novo);
EP-A-208,491 {Genencor) and WO-94/14951 (Novo). Although such systems should deliver both excellent starch and tannin removal, it has been observed that the mere replacement of standard enzymes with the bleach-resistant varieties in conventional formulations results in poorer, rather than improved, overall performance. A need still exists for stable compositions which deliver effective performance over a full range of soils and stains.
Cleaning systems which deliver both excellent starch and tannin removal have now been discovered. It has been found that selected oxygen bleaches formulated in a non-conventional pH range can meet these demanding performance targets. In addition, surprising synergistic interactions between certain bleaches, bleach resistant enzymes, builders and wash conditions have actually been found to enhance enzyme activity and improve enzyme stability to provide cleaning systems which deliver excellent performance over a full range of soils and stains.
Swaataxw of the Invention A warewashing detergent composition for use in both domestic and industrial dishwashing machines is described. The ' 3 composition comprises an organic monoperoxy or diperoxy acid which exhibits maximum tannin stain removal efficacy at a wash pH of about 8.5 which is at or near the pKa of the peroxy acid the organic peroxy acid being present in an amount of 1 ppm to 100 ppm available 02 in the solution;
an amylase enzyme which, when incubated at 55° C in a solution of 2 mM
sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half life of 10 minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405 nm of solution samples incubated with p-nitrophenyl-a-D-maltoheptaoside as substrate and gluco amylase and a-glucosidase as coupled enzymes; and 1 % by weight to 75% by weight of a builder, provided that a 1 % aqueous solution of the warewashing composition has a pH of 6 to 9.5.
Detailed description of the Preferred Embodiments The compositions of the invention may be in any form known in the art such as powder, tablet, block, liquid or gel. The compositions may also be produced by any conventional means.
Novel combinations of cleaning agents have been identified that will satisfy the demand for excellent starch and tannin removal from a single wash system. This system comprises an effective amount of a suitable organic peroxy acid, an effective amount of an amylase enzyme which, when incubated at 55°C in a solution of 2mM sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half-life of two minutes or greater based on an activity vs. time plot obtained via monitoring samples on a Roche Cobas Fara AnalyzerT'", using Roche ReagentT"", and about 1 to about 75 wt% of a builder, provided that a 1 aqueous solution of the detergent composition has a pH of from 6 to 9.
~erox~ Acids .
Since amylase enzymes are ineffective in a wash pH range of greater than about 10, it is necessary to be able to achieve good bleach performance in a wash having a pH value of less than about 10 in order to meet the dual criteria of excellent starch and excellent tannin removal.
It is also desirable to replace a halogen bleach with a peroxygen bleach to provide a milder and more environmentally friendly composition.
Typically, formulations based on oxygen bleaches include sodium perborate, sodium percarbonate or hydrogen peroxide.
These oxygen bleaches are preferably used in conjunction with a bleach activator to provide more effective bleaching at 15 temperatures of below about 60°C.
However, in the present invention, selection of the bleach moiety is critical. Despite claims that the bleach-resistant amylases are functional with a full range of bleaches, 20 excellent overall performance is not achieved with this range.
Thus, the bleaching performance of hydrogen peroxide (Ha02) decreases as the pH of the wash is reduced from about 12 to about 10. At pH 10, in short wash times, inclusion of H20a provides.no extra tannin removal benefits than could be obtained through the utilization of a strong builder such as nitrilotriacetate. Therefore, there is no advantage for a bleach-resistant amylase with hydrogen peroxide. In fact, at pH 10, the combination of Hz02/conventional amylase is more effective with regard to starch removal than the combination of H202/bleach-resistant amylase.
Peroxide/activator systems generally require a wash pH of about 10 in order to achieve rapid rates of perhydrolysis, ~ -.
something that would be essential at short wash times.
However, this requirement conflicts with the optimum conditions for starch removal since the activity of the novel bleach-resistant amylase is very low at wash pH's of about 10 5 and starch removal is poor.
Thus the oxygen bleach that is suitable for the invention must be a selected organic peroxyacid which has its maximum stain removal efficacy at a wash pH of about 8.5, which is generally at, or near, the pKa of the peracid, and wherein a 1% aqueous solution has a pH of from 6 to about 9.
Note that while peracetic acid (PAA) has a pKa of 8.2, its stain removal performance increases through the pH range 7 to 10. Thus, PAA would not be a preferred peracid bleach for use in the inventive system. The same would be true of peracid molecules with properties similar to monoperoxyphthalate and monopersulphate, which are very hydrophilic in nature and deliver poor tannin removal at low pH.
Typical organic peroxy acids which are useful include alkyl peroxy acids and aryl peroxy acids such as:
(i) peroxybenzoic acid and ring-substituted peroxybenzoic acids, e.g., peroxy-alpha-naphthoic acid.
(ii) aliphatic and substituted aliphatic moasoperoxy acids, e.g., peroxylauric acid, peroxystearic acid, epsilon-phthalimido peroxyhexanoic acid and o-carboxybenzamido peroxyhexanoic acid, N-nonenyl-amidoperadipic acid and N-nonenylamidopersuccinic acid.
Diperoxy acids may also be used as the organic peroxy acid and include alkyl peroxy acids and aryldiperoxy acids, such as:
(iii) 1,12-diperoxydodecanedioic acid (iv) 1,9-diperoxyazelaic acid , (v) diperoxybrassylic acid; diperoxysebacic acid and diperoxy-isophthalic acid , {vi) 2-decyldiperoxybutane-1,4-dioic acid (vii) N,N'-terephthaloyl-di(6-aminopercaproic acid).
Preferred organic peroxy acids include epsilon-phthalimidoperoxyhexanoic acid (PAP), o-carboxybenzamidoperoxyhexanoic acid, and mixtures thereof.
The organic peroxy acid is present in the composition in an amount such that the level of organic peroxy acid in the wash solution is 1 ppm to 100 ppm Av Ox, preferably 3 ppm to 50 ppm Av Ox, most preferably 5 ppm to 30 ppm Av Ox.
15-The organic peroxy acid may be incorporated directly into the formulation or may be encapsulated by any number of encapsulation techniques.
A preferred encapsulation method is described in US-A-5,200,236. In the patented method, the bleaching agent is encapsulated as a core in a paraffin wax material having a melting point from about 40°C to about 50°C. The wax coating has a thicl~ness of from 100 to 1500 microns.
Alpha (a) Amylase Enzymes An effective amount of an amylase enzymeis used which, when incubated at 55°C in a solution of 2mM sodium citrate, 1mM
epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH
8.0, has a half-life of two minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405nm of solution samples incubated with p-nitrophenyl-cx-D-maltoheptaoside as substrate and gluco amylase and a-glucosidose as coupled enzymes. A preferred monitor is the Roche Cobas Fara Analyzer using Roche Reagent.
' CA 02236881 2004-06-02 Preferably, the half-life of the enzyme is 5 minutes or greater, preferably 10 minutes or greater.
Such a-amylase enzymes with improved oxidation stability and bleach resistance useful in the invention are described in WO-94/02597 (Novo); WO-94/14951 (Novo) and EP-A-208,491 (Genencor International Inc.)_.
The a-amylase enzymes should be present in the detergent -i 10 composition in an amount providing an enzyme activity level in the wash solution of from about 50 mu/1 to about 5x10' mu/1, preferably from about 100 mu/1 is about 2x10' mu/1, more preferably from about 100 mu/1 to about 104 mu/1.
Amylolytic activity of the described a-amylases can be determined by a conventional method such as the one described in P. Bernfeld, Method of Enzymology, Vol. I (1995), pg. 149 The a-amylase is a mutated amylase wherein one or more methionine amino acid residues is exchanged with an amino acid residue except for cysteine or methionine.
A preferred type of the a-amylase is a Bacillus a-amylase.
More preferred types of the bleach resistant cx-amylase are Bacjllus Iicheniformis cx-amylase, B. amyloliquefaciens a-amylase and B. stearothermophilus cx-amylase, and furthermore Aspergillus aiger ar-amylase. It has been found that this entire group of mutant a-amylases exhibit a half-life of greater than two minutes under the test conditions outlined in the "Summary of the Invention".
A preferred embodiment of the mutant a-amylase is characterized by the fact that one or more of the methionine WO 97/18287 PC'1'/EP96J04659 amino acid residues is (are) exchanged with a Leu, Thr, Ala, Gly, Ser, Ile, or Asp amino acid residue, preferably a Leu, Thr, Ala, or Gly amino acid residue. In this embodiment a very satisfactory activity level and stability in the presence of the oxidizing agents is obtained.
A preferred embodiment of the mutant a-amylase is characterized by the fact that the methionine amino acid residue in position 197 in B. licheniformis a-amylase or the methionine amino acid residue in homologous positions in other cx-amylases is exchanged. The concept of homologous positions or sequence homology of cx-amylase has been explained e.g. in Nakajima, R. et al., 1986, Appl. Microbiol.
Biotechnol. ~, 355-360 and Liisa Holm et al., 1990, Protein Engineering 3, 181-191. Sequence homology of Bacillus a-amylases from B. licheniforms, B. stearothermophilus and B.
amyloliquefaciens are about 60%. This makes it possible to align the sequences in order to compare residues at homologous positions in the sequence. By such alignment of a-amylase sequences the number in each cx-amylase sequence of the homologous residues can be found. The homologous positions will probably spatially be in the same positions in a three dimensional structure (Greer, J., 1981, J. Mol. Biol.
153, 1027-1042) thus having analogous impact on specific functions of the enzyme in question. In relation to position 197 a.n B. licheniformis a-amylase, the homologous positions in B. stearothermophils a-amylase are positions 200 and 206, and the homologous position in B. amyloliquefaciens a-amylase is position 197. Experimentally it has been found that these mutuants exhibit both an improved activity level and an improved stability in the presence of oxidizing agents.
A preferred embodiment of the mutuant a-amylase according to the invention is characterized by the fact that one or both of the methionine amino acid residues in positions 200 and 206 in B. stearothermophiius a-amylase or the methionine amino acid residues in homologous positions in other a-amylases are exchanged. In relation to positions 200 and 206 in B. stearotherrnophilus a-amylase the homologous position in B. licheniforniis a-amylase is 197 and the homologous position in B. amyloliquefaciens a-amylase is position 197.
Experimentally it has been found that these mutants exhibit both an improved activity level and an improved stability in the presence of the oxidizing agents.
As illustrated in Example 2, 3 and 4 below, the preferred a-amylase was observed to exhibit a poor level of cleaning performance in a wash liquor having a pH of 10 or greater both in the presence and in the absence of an organic peroxy acid bleach (e. g., PAP). Thus, the improved bleach stability of the above described a-amylases gave little benefit in cleaning performance when the amylases are formulated in machine dishwashing compositions at pH levels greater than or equal to 14.
In order to obtain improved levels of starch removal with a detergent formulation containing a-amylases which are bleach resistant, it was observed that the pH of the wash liquor must be below 10, preferably 6 to 9.5, most preferably 7 to 9.5. (See Examples 5 and 6). As noted above, at a reduced alkalinity of less than pH 10, traditional peroxygen bleaching agents do not deliver a significant bleaching benefit.
Therefore, according to the invention the above described a-amylases must be formulated with an organic peroxy acid in a detergent composition, provided that a 1% aqueous solution of the detergent composition has a pH of from 6 to 9, to provide overall effective performance on both starch and tannin.
hetergent Builder Materials The compositions of this invention can contain all manner of detergent builders commonly taught for use in machine dishwashing or other cleaning compositions. The builders can 5 include any of the conventional inorganic and organic water-soluble builder salts, or mixtures thereof and may comprise 1 to 75%, and preferably, from about 5 to about 70%
by weight of the cleaning composition, 10 Typical examples of phosphorus-containing inorganic builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates and polyphosphates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, pyrophosphates and hexametaphosphates.
Suitable examples of non-phosphorus-containing inorganic builders, when present, include water-soluble alkali metal carbonates, bicarbonates, sesquicarbonates, borates, silicates, metasilicates, and crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate, sodium and potassium bicarbonates, silicates and zeolites.
Particularly preferred inorganic builders can be selected from the group consisting of sodium tripolyphosphate, potassium tripolyphosphate, potassium pyrophosphate, sodium, carbonate, potassium carbonate, sodium bicarbonate, sodium silicate and mixtures thereof, When present in these compositions, sodium tripolyphosphate concentrations will range from about 2% to about 40%; preferably from 5% to 30%.
Potassium tripolyphosphate concentrations will range from about 2% to about 50%, preferably from 5% to 40%. Sodium and potassium carbonate and bicarbonate when present can range from about 5% to about 50%; preferably from 10% to 30% by weight of the cleaning compositions. Sodium tripolyphosphate, potassium tripolyphosphate and potassium pyrophosphate can be used as builders in gel forntulations, where they may be present from 3 to 50%, preferably from 10 to 40%.
Organic detergent builders can also be used in the present invention. Examples of organic builders include alkali metal citrates, succinates, malonates, fatty acid sulfonates, fatty acid carboxylates, nitrilotriacetates, phytates, phosphonates, alkanehydroxyphosphonates, oxydisuccinates, alkyl and alkenyl disuccinates, oxydiacetates, carboxymethyloxy succinates, ethylenediaaaine tetraacetates, tartrate monosuccinates, tartrate disuccinates, tartrate monoacetates, tartrate diacetates, oxidized starches, oxidized heteropolymeric polysaccharides, polyhydroxysulfonates, polycarboxylates such as polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/ polymethacrylate copolymers, acrylate/
maleate/vinyl alcohol terpolymers, aminopolycarboxylates and polyacetal carboxylates, and polyaspartates and mixtures thereof. Such carboxylates are described in US-A-4,144,226, US-A-4,146,495 and US-A-4,686,062.
Alkali metal citrates, nitrilotriacetates, oxydisuccinates, polyphosphonates and acrylate/maleate copolymers and .
acrylate/maleate/vinyl alcohol terpolymers are especially preferred organic builders. When present they are preferably available from 1% to 35% of the total weight of the detergent compositions.
The foregoing detergent builders are meant to illustrate but not limit the types of builders that can be employed in the present invention.
The composition may also include an enzyme selected from the group consisting of a protease and a lipase in an effective amount to remove soils.
Anti-Scalant Scale formation on dishes and machine parts is an important problem that needs to be resolved or at least mitigated in formulating a machine warewashing product, especially in the case of low-phosphate (e.g. less than the equivalent of 20%
by weight, particularly 10°s by weight of sodium triphosphate) and phosphate-free machine warewashing compositions, particularly zero-P machine warewashing compositions.
In order to reduce this problem, co-builders, such as polyacrylic acids or polyacrylates (PAA), acrylate/maleate copolymers, and the various organic polyphosphonates, e.g. of the Dequest~" range, may be incorporated in one or more system components. For improved biodegradability, the block co-polymers of formula (I) as defined in WO-94/17170 may also be used. In any component, the amount of co-builder may be in the range of from 0.5 to 10, preferably from 0.5 to 5, and more preferably from 1 to 5°s by weight.
Surfactants Useful surfactants include anionic, nonionic, cationic, amphoteric, zwitterionic types and mixtures of these surface active agents. Such surfactants are well known in the .
detergent art and are described at length in "Surface Active Agents and Detergents", Vol. II, by Schwartz, Perry & Hirch, Interscience Publishers, Inc. 19591 Preferred surfactants are one or a mixture of:
Anionic surfactants Anionic synthetic detergents can be broadly described as surface active compounds with one or more negatively charged functional groups. An important class of anionic compounds are the water-soluble salts, particularly the alkali metal - salts, of organic sulfur reaction products having in their molecular structure an alkyl radical containing from about 6 to 24 carbon atoms and a radical selected from the group consisting of sulfonic and sulfuric acid ester radicals.
Primary A11cy1 Su1 fa tes Rl OSO~NI
where R' is a primary alkyl group of 8 to 18 carbon atoms and M is a solubilizing ration. The alkyl group R' may have a mixture of chain lengths. It is preferred that at least two thirds of the R' alkyl groups have a chain length of 8 to 14 carbon atoms. This will be the case if R1 is coconut alkyl, for example. The solubilizing ration may be a range of rations which are in general monovalent and confer water solubility. Alkali metal, notably sodium, is especially envisaged. Other possibilities are ammonium and substituted ammonium ions, such as trialkanol- or trialkyl-ammonium.
AIhy1 Ether Sulfates 2 0 RIO (CHaCH20) nSO~?
where R' is a primary alkyl group of 8 to 18 carbon atoms, n has an average value in the range from Z to 6 and M is a solubilizing ration. The alkyl group RI may have a mixture of chain lengths. It is preferred that at least two thirds of the RI alkyl groups have a chain length of 8 to 14 carbon atoms. This will be the case if RI is coconut alkyl, for example. Preferably n has an average value of 2 to 5.
Fatty Aci d Ester Sulfonates 3 0 RICH (S03M) CO~
where RZ.is an alkyl group of 6 to 16 atoms, R3 is an alkyl group of 1 to 4 carbon atoms and M is a solubilizing ration.
The group RZ may have a mixture of chain lengths. Preferably at least two thirds of these groups have 6 to 12 carbon WO 97/I$287 PCT/EP96/04659 atoms. This will be the case when the moiety RzCH(-)COZ(-) is -derived from a coconut source, for instance. It is preferred that .R3 is a straight chain alkyl, notably methyl or ethyl.
-AlJcy1 Benzene Sulfonates R'~ArS03hl where R4 is an alkyl group of 8 to 18 carbon atoms, Ar is a benzene ring (C6FI4) and M is a solubilizing cation. The group R'~ may be a mixture of chain lengths. Straight chains of 11 to 14 carbon atoms are preferred.
Organic phosphate based anionic surfactants include organic phosphate esters such as complex mono- or diester phosphates of hydroxyl- terminated alkoxide condensates, or salts thereof. Included in the organic phosphate esters are phosphate ester derivatives of polyoxyalkylated alkylaryl phosphate esters, of ethoxylated linear alcohols and ethoxylates of phenol. Also included are nonionic alkoxylates having a sodium alkylenecarboxylate moiety linked to a terminal hydroxyl group of the nonionic through an ether bond. Counterions to the salts of all the foregoing may be those of alkali metal, alkaline earth metal, ammonium, alkanolammonium and alkylammonium types.
Particularly preferred anionic surfactants are the fatty acid ester sulfonates with formula:
RzCH (SO3M) CO~
where the moiety RaCH(-) COa (-) is derived from a coconut source and R3 is either methyl or ethyl.
' Nonionic surfactants Nonionic surfactants can be broadly defined as surface active compounds with one or more uncharged hydrophilic substituents. A major class of nonionic surfactants are those compounds produced by the condensation of alkylene oxide groups with an organic hydrophobic material which may - be aliphatic or alkyl aromatic in nature. The length of the hydrophilic or polyoxyalkylene radical which is condensed 5 with any, particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
Illustrative, but not limiting examples, of various suitable nonionic surfactant types are:
polyoxyethylene or polyoxypropylene condensates of aliphatic carboxylic acids, whether linear- or branched-chain and unsaturated or saturated, containing from about 8 to about 18 carbon atoms in the aliphatic chain and incorporating from about 2 to about 50 ethylene oxide and/or propylene oxide units. Suitable carboxylic acids include "coconut" fatty acids (derived from coconut oil) which contain an average of about 12 carbon atoms, "tallow" fatty acids (derived from tallow-class fats) which contain an average of about 18 carbon atoms, palmitic acid, myristic acid, stearic acid and lauric acid, polyoxyethylene or polyoxypropylene condensates of aliphatic aleohols, whether linear- or branched-chain and unsaturated or saturated, containing from about 6 to about 24 carbon atoms and incorporating from about 2 to about 50 ethylene oxide and/or propylene oxide units. Suitable alcohols include "coconut" fatty alcohol, "tallow" fatty alcohol, lauryl alcohol, myristyl alcohol and oleyl alcohol.
Ethoxylated fatty alcohols may be used alone or in admixture - with anionic surfactants, especially the preferred surfactants above. The average chain lengths of the alkyl group Rs in the general formula:
RSO (CH2CHa0) nH
is from 6 to 20 carbon atoms. Notably the group RS may have chain lengths in a range from 9 to 18 carbon atoms. _ The average value of n should be at least 2. The numbers of ethylene oxide residues may be a statistical distribution around the average value. However, as is known, the distribution can be affected by the manufacturing process or altered by fractionation after ethoxylation. Particularly preferred ethoxylated fatty alcohols have a group RS which has 9 to 18 carbon atoms while n is from 2 to 8.
Also included within this category are nonionic surfactants having a formula:
Rd-(CH2CHU),~(CHsCH20)y(CIi~CHt~~yH
l~t~ Rs wherein R6 is a linear alkyl hydrocarbon radical having an average of 6 to 18 carbon atoms, R' and R$ are each linear alkyl hydrocarbons of about 1 to about 4 carbon atoms, x is an integer of from 1 to 6, y is an integer of from 4 to 20 ~.nd z is an integer from 4 to 25.
A preferred nonionic surfactant of the above formula is Poly-Tergent SLF-18' a registered trademark of the Olin Corporation, New Haven, Conn. having a composition of the above formula where R6 is a C6-Clo linear alkyl mixture, R' and Rg are methyl, x averages 3, y averages 12 and z averages 16.
Another preferred nonionic surfactant is WO 97!18287 PCT/EP96/04659 R90 {CHsCHQ) j{CHsCH2U)k{CHy CH{dH}R1o)1 I
CHI
wherein R9 is a linear, aliphatic hydrocarbon radical having from about 4 to about 18 carbon atoms including mixtures thereof; and R1° is a linear, aliphatic hydrocarbon radical having from about 2 to about 26 carbon atoms including mixtures thereof; j is an integer having a value of from 1 to about 3; k is an integer having a value from 5 to about 30;
and z is an integer having a value of from 1 to about 3.
Most preferred are compositons in which j is 1, k is from about 10 to about 20 and 1 is 1. These surfactants are described in WO-94/22800. Other preferred nonionic surfactants are linear fatty alcohol alkoxylates with a capped terminal group, as described in US-A-4,340,766.
Particularly preferred is Plurafac LF403 ex. BASF.
polyoxye~thylene or polyoxypropylene condensates of alkyl phenols, whether linear- or branched-chain and unsaturated or saturated,containing from about 6 to 12 carbon atoms and incorporating from about 2 to about 25 moles of ethylene oxide and/or propylene oxide.
polyoxyethylene derivatives of sorbitan mono-, d3-, and tri-fatty acid esters wherein the fatty acid component has between 12 and 24 carbon atoms. The preferred polyoxyethylene derivatives are of sorbitan monolaurate, sorbitan trilaurate, sorbitan monopalmitate, sorbitan tripalmitate, sorbitan monostearate, sorbitan ~monoisos.tearate, sorbitan tripalmitate, sorbital tristearate, t sorbitan monooleate, and sorbitan trioleate. The polyoxyethylene chains may contain between about 4 and 30 ethylene oxide units, preferably about 10 to 20. The sorbitan ester derivatives contain 1, 2 or 3 polyoxyethylene chains dependent upon whether they are mono-, di- or tri-acid esters.
polyoxyethylene-polyoxypropylene block copolymers having formula:
HO ( CHaCHaO ) , ( CH ( CH3 ) CH~O ) b ( CH2CHa0 ) ~H
or HO ( CH ( CH3 ) CHaO ) d ( CH2CHa0 ) ~ ( CH ( CH3 ) CHZO ) fFi to wherein a, b, c, d, a and f are integers from 1 to 350 reflecting the respective polyethylene oxide and poly-propylene oxide blocks of said polymer. The polyoxyethylene component of the block polymer constitutes at least about 10~
of the block polymer. The material preferably has a molecular weight of between about 1,000 and 15,000, more preferably from about 1,500 to about 6,000_ These materials are well-known in the art. They are available under the trademark "Pluronic" and "Pluronic R", a product of BASF Corporation.
Amine oxides having formula:
Ri2RisRi4N=O
wherein R12, Rts and Rt4 are saturated aliphatic radicals or substituted saturated aliphatic radicals. Preferable amine oxides are those wherein R'2 is an alkyl chain of about 10 to about 20 carbon atoms and R13 and R14 are methyl or ethyl groups or both R12 and RI3 are alkyl chains of about 6 to about 14 carbon atoms and R14 is a methyl or ethyl group_ .Amphoteric synthetic detergents can be broadly described as derivatives of aliphatic and tertiary amines, in which the aliphatic radical may be straight chain or branched and wherein one of the aliphatic substituents contain from about 8 to about 18 carbons and one contains an anionic water-solubilizing group, i.e., carboxy, sulpho, sulphato, phosphato or phosphono. Examples of compounds falling within this definition are sodium 3-dodecylamino propionate and sodium 2-dodecylamino propane sulfonate.
Zwitterionic synthetic detergents can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium and sulphonium compounds in which the aliphatic radical may be straight chained or branched, and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic water-solubilizing group, e.g., carboxy, sulpho, sulphato, phosphato or phosphono. These compounds are frequently referred to as betaines. Besides alkyl betaines, alkyl amino and alkyl amido betaines are encompassed within this invention.
AIIzy1 Glycosides l2rSG (R16O) " ~ZI ) p wherein Ris is a monovalent organic radical (e.g., a monovalent saturated aliphatic, unsaturated aliphatic or aromatic radical such as alkyl, hydroxyalkyl, alkenyl, hydroxyalkenyl, aryl, alkylaryl, hydroxyalkylaryl, arylalkyl, alkenylaryl, arylalkenyl, etc.) containing from about 6 to about 30 (preferably from about 8 to 18 and more preferably from about 9 to about 13) carbon atoms; R'6 is a divalent hydrocarbon radical containing from 2 to about 4 carbon atoms such as ethylene, propylene or butylene (most preferably the unit (Rr60)n represents repeating units of ethylene oxide, propylene oxide and/or random or block combinations thereof);
n is a number having an average value of from 0 to about 12;
ZI represents a moiety derived from a reducing saccharide containing 5 or 6 carbon atoms (most preferably a glucose unit); and p is a number having an average value of from 0.5 to about 10 preferably from about 0.5 to about 5 .
Examples of commercially available materials from Her~lcel Kommanditgesellschaft Alctien of Dusseldorf, Germany include APG° 300, 325 and 350 with R15 being C9-C11, n is 0 and p is 1.3, 1.6 and 1.8-2.2 respectively; APG° 500 and 550 with Rls 5 is C12-C13, n is 0 and p is 1.3 and 1.8-2.2, respectively; and APG° 600 with Rls being CIa-C14, n is 0 and p is 1.3.
While esters of glucose are contemplated especially, it is envisaged that corresponding materials based on other 10 reducing sugars, such as galactose and mannose are also suitable.
Particularly preferred anionic surfactants are the fatty acid ester sulfonates with formula:
15 RICH (S03M) CO~
where the moiety RZCH(-) COa (-) is derived from a coconut source and .R~ is either methyl or ethyl.
The amount of glycoside surfactant, anionic surfactant 20 andJor ethoxylated fatty alcohol surfactant will be from 0.5 to 40~ by weight of the composition. Desirably the total amount of surfactant lies in the same range. The preferred range of surfactant is from 0.5 to 30~ by weight, more preferably from 0.5 to 15~ by weight.
ill r An inert particulate filler material which is water-soluble may also be present in cleaning compositions. This material should not precipitate calcium or magnesium ions at the filler use level. Suitable for this purpose are organic or inorganic compounds. Organic fillers include sucrose esters and urea. Representative inorganic fillers include sodium sulfate, sodium chloride and potassium chloride. A preferred filler is sodium sulfate. Its concentration may range from 0% to 60%, preferably from about 5% to about 30% by weight of the cleaning composition.
Thickeners and Stabilizers Thickeners are often desirable for liquid cleaning compositions. Thixotropic thickeners such as smectite clays including montmorillonite (bentonite), hectorite, saponite, and the like may be used to impart viscosity to liquid cleaning compositions. Silica, silica gel, and alumino-l0 silicate may also be used as thickeners. Salts of polyacrylic acid (of molecular weight of fr~a about 300, 000 up to 6 million and higher), including polymers which are cross-linked may also be used alone or in combination with other thickeners. Use of clay thickeners for machine dishwashing compositions is disclosed for example in US-A-4,431,559; US-A-4,511,487; US-A-4,740,327; US-A-4,752,409.
Commercially available synthetic smectite clays include Laponite supplied by Laporte Industries. Commercially available bentonite clays include Korthix Hue' and VWH ex Combustion Engineering, Inc.; Polargel T'" ex American Colloid'.
Co.; and Gelwhite'" clays (particularly Gelwhite GP and H) ex English China Clay Co. Polargel T is preferred as imparting a more intense white appearance to the composition than other clays. The amount of clay thickener employed in the compositions is from 0.1 to 10%, preferably 0.5 to 5%. Use of salts of polymeric carboxylic acids is disclosed for example in GH-A-2,164,350A, US-A-4,859,358 and US-A-4,836,948.
For liquid formulations with a 'gel" appearance and rheology, particularly if a clear gel is desired, a chlorine-resistant polymeric thickener is particularly useful. USA-4,260,528 discloses natural gums and resins for use in clear machine dishwashing detergents, which are not chlorine stable. Acrylic acid polymers that are cross-linked WO 97/18287 PCTIEP96lOd659 manufactured by, for example, B.F. Goodrich and sold under the trade name "Carbopol" have been found to be effective for production of clear gels, and Carbopol 940, 617 and 627, having a molecular weight of about 4,000,000 are particularly preferred for maintaining high viscosity with excellent chlorine stability over extended periods. Further suitable chlorine-resistant polymeric thickeners are described in US-A-4,867,896. The amount of thickener employed in the compositions is from 0 to 5%, preferably 0.5-3%.
i Stabilizers and/or co-structuraats such as long=chain calcium and sodium soaps and C~x to Cls sulfates are detailed in US-A-3,956,158 and US-A-4,271,030 and the use of other metal salts of long-chain soaps is detailed in US-A-4,~~2,409o Qther co-structurants include Laponite and metal oxides and their salts as described in US-A-4,933,101. The amount of stabilizer which may be used in the liquid cleaning compositions is from 0.01 to 5% by weight of the composition, preferably 0.01-2%. Such stabilizers are optional in gel formulations. Co-structurants which are found especially suitable for gels include trivalent metal ions at 0.01-4% of the compositions, Laponite and/or water-soluble structuring chelants at 0.01-5%. These co-structurants are more fully described in US-A-5,141,664.
Anti-TarnishinoLAqents Anti-tarnishing agents may be incorporated into the compositions. Such agents include benzotriazole, certain 1,3 N-azoles described in US-A-5,480,576; isocyanuric acid described in US-A-5,374,369; and purine compounds described in US-A-5,468,410.
Defoamer The formulations of the cleaning composition comprising surfactant may further include a defoamer. Suitable defoamers include mono-and distearyl acid phosphate, silicone oil and mineral oil. Even if the cleaning composition has only defoaming surfactant, the defoamer assists to minimize foam which food soils can generate. The compositions may include 0.02 to 2% by weight of defoamer, or preferably 0.05-1.0%.
Optional Ingredients Minor amounts of various other components may be present in the cleaning composition. These include bleach scavengers including but not limited to sodium bisulfate, sodium perborate, reducing sugars, and short chain alcohols;
solvents and hydrotropes such as ethanol, isopropanol and xylene sulfonates; flow control agents (in granular forms);
enzyme stabilizing agents; soil suspending agents;
antiredeposition agents; anti-corrosion agents; ingredients ~~ enhance decor care such as certain aluminum salts described in WO-96/36687 and US-A-5624892; colorants;
perfumes; and other functional additives.
The following examples will serve to distinguish this invention from the prior art and illustrate its embodiments more fully. Unless otherwise indicated, all parts, percentages and proportions referred to are by weights.
The half-lives of amylases were determined by the method in the specification. Thus, the amylase, at a level of 4x10'mu/1, was incubated at 55°C in a solution containing 2mM
sodium citrate, 1mM sodium citrate, 1mM epsilon phthalimidoperoxyhexanoic acid and 36 ppm hardness ions with a calcium to magnesium ratio of 4:1 and maintained at pH 8Ø
Samples were withdrawn at suitable intervals and analyzed for enzyme activity on a Roche Cobas Fara Analyzer using Roche S Reagent. This contains p-nitrophenyl-a-D-maltoheptaoside as the substrate which is hydrolyzed by the amylase in question to give p-nitrophenylmaltotriose. This moiety is then hydrolyzed by glycoamylase to p-nitrophenylmaltotriose, which in turn is hydrolyzed by gluco amylase to p-nitrophenyl glycoside aad further hydrolyzed by a-glucosideose to p-nitrophenol. The absorbance of p-nitrophenol is measured at 405nm.
The results for Termanyl°", Duramyl'" and Purafect ~ OxAm 4000 G
(ex. Genencor) are given in Table 1.
Termamyl Duramyl Purafect~ OxAm <1 13 >20 Thus, Termamyl is outside the scope of the invention.
EXAMPhE 2 The amylolytic activity and starch removal performance of a bleach resistant a-amylase (Duramyl~", supplied by Novo) was compared to that of~a conventional amylase (i.e. Termamyl, supplied by Novo) under model wash conditions in a beaker at pH 10, 55°C.
Two detergent compositions were prepared, including an amount of Duramyl'~ and Termanyl~' to provide an enzymatic activity level of 220 Maltose units per liter in the wash solution.
Also included in the compositions were 0.2g/1 sodium ' CA 02236881 2004-06-02 nitrilotriacetate and carbonate/bicarbonate buffer containing 1.7g/1 of NazC03.10Hs0 and 0.34g/1 of NaHC03. No bleaching agent was added to either sample. The pH of an aqueous solution of each of the compositons was adjusted to 5 pH 10 with NaOH or HzSO, as needed.
The amylolytic activity of the two types of enzyme was determined as follows:
Model wash solutions containing carbonate/bicarbonate buffer, 10 builder (if present) and hardness ions (if present) are ' stirred in a constant temperature jacketed beaker. Enzyme and bleach (if present) are added. Samples are withdrawn from this solution at fixed times and added to solid starch azure, a crystalline potato starch polymer linked with 15 Remazol"" Brilliant Blue. This.mixture is incubated for a set time, centrifuged and the color development in the supernatant measured. This experiment measures the change in enzyme activity over time.
Absorbance values were recorded over a 60 minute time period.
20 The greater the absorbance value, the higher the activity of the enzyme in the composition. The following results were obtained at pH 10.
Absorbaace at 59611m (or Amylase Activity) Elapsed time (min) Duramyl Termamyl _ ._._ ._ i 0 0.44 1.23 10 0.53 1.17 20 0.27 1.24 30 0.29 1.23 40 0.25 1.23 50 0.23 1.30 60 0.22 1.26 At pH 10, with no bleach present, the conventional amylase exhibited a significantly higher enzymatic activity than the composition containing the a-amylase of the present -invention.
The starch removal performance of the two samples was also compared in an industrial dishwasher by washing three racks of dishes, each rack being loaded with a range of dishware that included ten starch-soiled plates. The components of the cleaning composition were dosed into the machine just once, prior to washing the first rack of dishes. Since there was no further dosing of product, each successive wash resulted in a 10~ dilution of the product concentration due to the introduction of fresh rinse water at the end of each main wash. There was a waiting period of 5 minutes between the processing of the second and third racks of dishes. The level of residual starch was assessed visually after disclosure of the washed plate in iodine solution.
SUBSTITUTE SHEET (RULE 26) Termamyl 300L and Duramyl 300L were each dosed to give 4 x 103 Mu/Q in the wash. The following results were obtained.
Residual Starch (~ Area ) Sample Rack 1 Rack 2 Rack 3 Termamyl 300L 13 13 12 Duramyl 300L 100 100 100 Consistent with the observed amylolytic activity profiles above, at a wash pH of 10 and in the absence of bleach, the composition containing the conventional amylase, Termamyl 300L, was observed to give significantly better starch removal performance than the novel a-amylase when both were incorporated in a detergent composition as described above.
FXaMT~T.F 3 The compositions of Example 2 were modified by incorporating hydrogen peroxide (100 ppm Av Ox) or hypochlorite (60 ppm Av.
Cl) as bleaching agent. Three racks of soiled dishware were washed as described in Example 2 and evaluated for residual starch soil with the following results.
SUBSTITUTE SHEET (RULE 26) WO 97/18287 PCT/EP96/a4659 Residual ' Starch ( ~SArea ) Bleach Eazyme Rack Raek 2 Rack Hypochlorite Termamyl 300L 100 100 100 Duramyl 300L 100 100 100 Hydrogen Termamyl 300L 7 8 10 Peroxide Duramyl 300L 100 100 100 Chlorine bleach has a devastating impact on the stability of both amylase variants and so the cleaning results are poor in both cases. There is a big improvement in enzyme stability rahen the bleach is hydrogen peroxide. However, the starch removal performance of both enzymes remained essentially unchanged relative to the composition with no bleach described in Example 2. Thus, a.n the presence of hydrogen peroxide at pH 10, it is the conventional amylase, not the bleach-resistant amylase that gives the better starch removal performance.
Epsilon-phthalimido peroxyhexanoic acid (PAP) and peracetic acid (PAA) were both used in lieu of the hydrogen peroxide as peroxygen bleaching agent in the sample of Example 2 containing the Duramyl a-amylase. The pH of the wash solution was adjusted to a value of 10. The starch removal performance of the composition containing Duramyl and these peracids was also observed after three washing cycles as described in Example 2. Residual starch levels were 70, 100 and 95~ respectively, when the bleaching agent was PAP, and were 15, 100 and 100 respectively when the bleaching agent was PAA.
Therefore, substituting the conventional oxygen bleaching agent, hydrogen peroxide, with a more powerful peracid bleaching agent (PAP or PAA) did not significantly improve the starch removal performance of the Duramyl cx-amylase when formulated in a detergent composition at pH 10, and therefore at this wash pH there is still no benefit for this novel cx-amylase over the conventional Termamyl amylase.
The amylolytic activity of both a bleach-resistant amylase and Termamyl were monitored at a wash pH of 8.5, both in the absence and presence of PAP. The technique used a.s the same as that described in Example 2. The relative amylase activities, based on absorbancies, are given in Table 6.
Relative Amylase Activity at pH
8.5 Elapsed Duramyl Duramyl Termamyl Termamyl 5 Time + PAP + PAP
(minutes) 0 1.25 2.5 0.75 0.75 5 1.0 2.4 1.0 0.5 10 1.0 2.25 1.0 0.8 15 0.85 1.7 1.0 0.2 10 20 0.90 1.25 1.0 0.2 30 1.0 1.0 1.0 0.2 Unexpectedly, the amylolytic activity of the formulation containing the a-amylase according to the invention was 15 synergistically enhanced by addition of the peracid at pH
8.5. In contrast, the activity of Termamyl decreased on addition of the PAP. This enhancement between the bleach-resistant amylase and PAP did not occur at pH 10, as seen from the absorbance data in Table 6.
SUBSTITUTE SHEET (RULE 26) RELATIVE AMYLASE
ACTIVITY AT
pH 3Ø0 Elapsed time Duramyl Duramyl + PAP
(minutes) 0 0.14 0.06 5 0.11 0.05 0.12 0.10 0.08 0.18 10 20 0.06 0.04 30 0.06 0.05 Again, this is surprising since one would have expected that as the pH moved down from pH 10 to pH 8.5, that is as 15 the pH moved to the range of greatest activity for PAP, the effect on Duramyl would be negative, not positive. Also, this positive synergistic benefit on the bleach-resistant amylase activity occurs at the pH region where the functionality of PAP (i.e. bleaching of tannin} is optimum.
The starch and tannin removal performance profiles were determined for a bleach-resistant a-amylase in combination with a wide range of peracid bleaching agents (i.e.
hydrophobic monoperoxy- and diperoxy-acids; hydrophilic monoperoxy acid; inorganic peroxyacid).
The cleaning experiments were conducted in a domestic dishwashing machine wherein the wash temperature was SUBSTITUTE SHEET (RULE 26) maintained at 55°C and the wash pH at 8.5 (with borate buffer) or 10 (with carbonate/bicarbonate buffer). In one type of experiment where only four times stained tea cups were included, the wash time was 30 seconds. In a second =teat, where a combination of soiled tea cups and starch soiled plates were included, the wash time was 2 minutes.
The results of these tests are given in Table 8.
30 second 2 minute wash wash PERACID Wash Residual Residual Residual pii Tea+ Tea+ Starch PAP 8.5 0 0 45 TPCAP* 8.5 0.7 0.8 39 DPDDA** 8.5 1.0 0_3 37 H48*** 8.5 2.4 1.5 26 H48 10 1.5 - -KMPS**** 8.5 2.9 2.0 34 KMPS 10 2.0 - -* N,N~-terephthaloyl-di (6-amino percaproic acid) ** 1,12-diperoxydodecanedioic acid *** magnesium monoperoxyphthalate **** potassium monopersulfate +The stained tea cups are rated on a zero (no residual stain) to five (heavy stain) scale. The difference between SUBSTITUTE SHEET (RULE 26) zero and non-zero tea scores is considered to be highly significant because any residual tea stain rapidly builds up during subsequent re-use and re-washing steps.
With regard to starch removal, the foregoing was designed to be a highly stressed performance test in order to clearly demonstrate differences. Differences in the starch removal scores for KMPS, DPDDA, TPCAP, PAP and H48 systems at pH 8.5 are considered to be small and all systems are capable of giving good levels of starch removal. However, there were significant differences in tannin removal. H48 and KMPS gave very poor levels of tannin removal at pH 8.5 and PAP was significantly better than both DPDDA and TPCAP.
Thus, the system that gives overall the best tannin and starch cleaning profile is the PAP/amylase system with the other hydrophobic peracid/enzyme combinations some distance behind.
2 0 E~CAMPLE 7 Surprisingly, it is found that the stability of Duramyl towards bleach is greatly enhanced when builder is present in the wash solution. A similar enhanced stability was not observed with Termamyl. The amyloyltic activity was monitored by the following method:
Starch azure, a crystalline potato starch polymer linked with Remazol Brilliant Blue, is heated in distilled water at 80°C for 15 minutes and transferred to glass slides (1 inch x 1 inch) which are then dried at room temperature overnight.
The slides are weighed. Model wash solutions containing pH
8.5 borate buffer, builder (at 0.56g/1 if present) and hardness ions (36ppm expressed as CaC03; 4:1 Ca:Mg ratio) are stirred and maintained at 55°C in a constant temperature jacketed beaker. Three retrograded starch slides are added , to the beaker, followed by either Duramyl or Ternaa.myl and then PAP (at 1mM). The absorbance of aliquots are measured , at 596 nm to give an assessment of in-wash enzyme activity.
In addition, at the end of the experiment, the slides are dried and weighed to determine the level of soil removal.
The builders evaluated were sodium nitrilotriacetate, sodium citrate and an acrylate/maleate/vinyl alcohol terpolymer from Huls, described in U.S_ 4,686,062. The activity of the enzymes was followed over a period of 30 minutes. The results are shown in Table 9.
Ingredients A B C D E F G H
NTA X J X X X J X X
5 Citrate X X ~ X X X J X
Huls X X X J X X X J
Polymer Duramyl J J J J X X X X
Termamyl X X X X J J J J
Time Residual (minutes) Amylolytic Activity 0 100 10 100 l0 100 10 10 100 J means present in the wash solution.
* X means absent from the wash solution.
Good stability of the bleach-resistant amylase in the presence of bleach is only obtained when builder is present SUBSTITUTE SHEET (RULE 26) in the wash solution (see B, C and D compared to A)_ A
similar enhancement of the stability of Termamyl, ~
traditional amylase, is not observed (see F, G, H compared to E) .
Using the same procedure outlined in Example 7, the effect of water hardness on the stability of a bleach-resistant amylase in the presence of 2mM NTA and 20 ppm Av Ox PAP was evaluated at 65°C. The activity of Duramyl was followed over 30 minutes. The results are shown in Table 10.
Table 10 Resish.al Amyl of y~ic Ac~iv3.tv Time Water Hardness (min.) (expressed as CaC03;
4:1 Ca: Mg ratio) i 0 ppm 10 ppm 36 ppm 80 ppm This demonstrates that hardness ions have a beneficial effect on the amylolytic stability of the bleach-resistant K
enzyme in the presence of builder and PAP.
SUBSTITUTE SHEET (RULE 26)
Bleach resistant amylase enzymes described in the art may be incorporated with either halogen or peroxygen bleaches in a detergent composition, as described in WO-94/02597 {Novo);
EP-A-208,491 {Genencor) and WO-94/14951 (Novo). Although such systems should deliver both excellent starch and tannin removal, it has been observed that the mere replacement of standard enzymes with the bleach-resistant varieties in conventional formulations results in poorer, rather than improved, overall performance. A need still exists for stable compositions which deliver effective performance over a full range of soils and stains.
Cleaning systems which deliver both excellent starch and tannin removal have now been discovered. It has been found that selected oxygen bleaches formulated in a non-conventional pH range can meet these demanding performance targets. In addition, surprising synergistic interactions between certain bleaches, bleach resistant enzymes, builders and wash conditions have actually been found to enhance enzyme activity and improve enzyme stability to provide cleaning systems which deliver excellent performance over a full range of soils and stains.
Swaataxw of the Invention A warewashing detergent composition for use in both domestic and industrial dishwashing machines is described. The ' 3 composition comprises an organic monoperoxy or diperoxy acid which exhibits maximum tannin stain removal efficacy at a wash pH of about 8.5 which is at or near the pKa of the peroxy acid the organic peroxy acid being present in an amount of 1 ppm to 100 ppm available 02 in the solution;
an amylase enzyme which, when incubated at 55° C in a solution of 2 mM
sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half life of 10 minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405 nm of solution samples incubated with p-nitrophenyl-a-D-maltoheptaoside as substrate and gluco amylase and a-glucosidase as coupled enzymes; and 1 % by weight to 75% by weight of a builder, provided that a 1 % aqueous solution of the warewashing composition has a pH of 6 to 9.5.
Detailed description of the Preferred Embodiments The compositions of the invention may be in any form known in the art such as powder, tablet, block, liquid or gel. The compositions may also be produced by any conventional means.
Novel combinations of cleaning agents have been identified that will satisfy the demand for excellent starch and tannin removal from a single wash system. This system comprises an effective amount of a suitable organic peroxy acid, an effective amount of an amylase enzyme which, when incubated at 55°C in a solution of 2mM sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half-life of two minutes or greater based on an activity vs. time plot obtained via monitoring samples on a Roche Cobas Fara AnalyzerT'", using Roche ReagentT"", and about 1 to about 75 wt% of a builder, provided that a 1 aqueous solution of the detergent composition has a pH of from 6 to 9.
~erox~ Acids .
Since amylase enzymes are ineffective in a wash pH range of greater than about 10, it is necessary to be able to achieve good bleach performance in a wash having a pH value of less than about 10 in order to meet the dual criteria of excellent starch and excellent tannin removal.
It is also desirable to replace a halogen bleach with a peroxygen bleach to provide a milder and more environmentally friendly composition.
Typically, formulations based on oxygen bleaches include sodium perborate, sodium percarbonate or hydrogen peroxide.
These oxygen bleaches are preferably used in conjunction with a bleach activator to provide more effective bleaching at 15 temperatures of below about 60°C.
However, in the present invention, selection of the bleach moiety is critical. Despite claims that the bleach-resistant amylases are functional with a full range of bleaches, 20 excellent overall performance is not achieved with this range.
Thus, the bleaching performance of hydrogen peroxide (Ha02) decreases as the pH of the wash is reduced from about 12 to about 10. At pH 10, in short wash times, inclusion of H20a provides.no extra tannin removal benefits than could be obtained through the utilization of a strong builder such as nitrilotriacetate. Therefore, there is no advantage for a bleach-resistant amylase with hydrogen peroxide. In fact, at pH 10, the combination of Hz02/conventional amylase is more effective with regard to starch removal than the combination of H202/bleach-resistant amylase.
Peroxide/activator systems generally require a wash pH of about 10 in order to achieve rapid rates of perhydrolysis, ~ -.
something that would be essential at short wash times.
However, this requirement conflicts with the optimum conditions for starch removal since the activity of the novel bleach-resistant amylase is very low at wash pH's of about 10 5 and starch removal is poor.
Thus the oxygen bleach that is suitable for the invention must be a selected organic peroxyacid which has its maximum stain removal efficacy at a wash pH of about 8.5, which is generally at, or near, the pKa of the peracid, and wherein a 1% aqueous solution has a pH of from 6 to about 9.
Note that while peracetic acid (PAA) has a pKa of 8.2, its stain removal performance increases through the pH range 7 to 10. Thus, PAA would not be a preferred peracid bleach for use in the inventive system. The same would be true of peracid molecules with properties similar to monoperoxyphthalate and monopersulphate, which are very hydrophilic in nature and deliver poor tannin removal at low pH.
Typical organic peroxy acids which are useful include alkyl peroxy acids and aryl peroxy acids such as:
(i) peroxybenzoic acid and ring-substituted peroxybenzoic acids, e.g., peroxy-alpha-naphthoic acid.
(ii) aliphatic and substituted aliphatic moasoperoxy acids, e.g., peroxylauric acid, peroxystearic acid, epsilon-phthalimido peroxyhexanoic acid and o-carboxybenzamido peroxyhexanoic acid, N-nonenyl-amidoperadipic acid and N-nonenylamidopersuccinic acid.
Diperoxy acids may also be used as the organic peroxy acid and include alkyl peroxy acids and aryldiperoxy acids, such as:
(iii) 1,12-diperoxydodecanedioic acid (iv) 1,9-diperoxyazelaic acid , (v) diperoxybrassylic acid; diperoxysebacic acid and diperoxy-isophthalic acid , {vi) 2-decyldiperoxybutane-1,4-dioic acid (vii) N,N'-terephthaloyl-di(6-aminopercaproic acid).
Preferred organic peroxy acids include epsilon-phthalimidoperoxyhexanoic acid (PAP), o-carboxybenzamidoperoxyhexanoic acid, and mixtures thereof.
The organic peroxy acid is present in the composition in an amount such that the level of organic peroxy acid in the wash solution is 1 ppm to 100 ppm Av Ox, preferably 3 ppm to 50 ppm Av Ox, most preferably 5 ppm to 30 ppm Av Ox.
15-The organic peroxy acid may be incorporated directly into the formulation or may be encapsulated by any number of encapsulation techniques.
A preferred encapsulation method is described in US-A-5,200,236. In the patented method, the bleaching agent is encapsulated as a core in a paraffin wax material having a melting point from about 40°C to about 50°C. The wax coating has a thicl~ness of from 100 to 1500 microns.
Alpha (a) Amylase Enzymes An effective amount of an amylase enzymeis used which, when incubated at 55°C in a solution of 2mM sodium citrate, 1mM
epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH
8.0, has a half-life of two minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405nm of solution samples incubated with p-nitrophenyl-cx-D-maltoheptaoside as substrate and gluco amylase and a-glucosidose as coupled enzymes. A preferred monitor is the Roche Cobas Fara Analyzer using Roche Reagent.
' CA 02236881 2004-06-02 Preferably, the half-life of the enzyme is 5 minutes or greater, preferably 10 minutes or greater.
Such a-amylase enzymes with improved oxidation stability and bleach resistance useful in the invention are described in WO-94/02597 (Novo); WO-94/14951 (Novo) and EP-A-208,491 (Genencor International Inc.)_.
The a-amylase enzymes should be present in the detergent -i 10 composition in an amount providing an enzyme activity level in the wash solution of from about 50 mu/1 to about 5x10' mu/1, preferably from about 100 mu/1 is about 2x10' mu/1, more preferably from about 100 mu/1 to about 104 mu/1.
Amylolytic activity of the described a-amylases can be determined by a conventional method such as the one described in P. Bernfeld, Method of Enzymology, Vol. I (1995), pg. 149 The a-amylase is a mutated amylase wherein one or more methionine amino acid residues is exchanged with an amino acid residue except for cysteine or methionine.
A preferred type of the a-amylase is a Bacillus a-amylase.
More preferred types of the bleach resistant cx-amylase are Bacjllus Iicheniformis cx-amylase, B. amyloliquefaciens a-amylase and B. stearothermophilus cx-amylase, and furthermore Aspergillus aiger ar-amylase. It has been found that this entire group of mutant a-amylases exhibit a half-life of greater than two minutes under the test conditions outlined in the "Summary of the Invention".
A preferred embodiment of the mutant a-amylase is characterized by the fact that one or more of the methionine WO 97/18287 PC'1'/EP96J04659 amino acid residues is (are) exchanged with a Leu, Thr, Ala, Gly, Ser, Ile, or Asp amino acid residue, preferably a Leu, Thr, Ala, or Gly amino acid residue. In this embodiment a very satisfactory activity level and stability in the presence of the oxidizing agents is obtained.
A preferred embodiment of the mutant a-amylase is characterized by the fact that the methionine amino acid residue in position 197 in B. licheniformis a-amylase or the methionine amino acid residue in homologous positions in other cx-amylases is exchanged. The concept of homologous positions or sequence homology of cx-amylase has been explained e.g. in Nakajima, R. et al., 1986, Appl. Microbiol.
Biotechnol. ~, 355-360 and Liisa Holm et al., 1990, Protein Engineering 3, 181-191. Sequence homology of Bacillus a-amylases from B. licheniforms, B. stearothermophilus and B.
amyloliquefaciens are about 60%. This makes it possible to align the sequences in order to compare residues at homologous positions in the sequence. By such alignment of a-amylase sequences the number in each cx-amylase sequence of the homologous residues can be found. The homologous positions will probably spatially be in the same positions in a three dimensional structure (Greer, J., 1981, J. Mol. Biol.
153, 1027-1042) thus having analogous impact on specific functions of the enzyme in question. In relation to position 197 a.n B. licheniformis a-amylase, the homologous positions in B. stearothermophils a-amylase are positions 200 and 206, and the homologous position in B. amyloliquefaciens a-amylase is position 197. Experimentally it has been found that these mutuants exhibit both an improved activity level and an improved stability in the presence of oxidizing agents.
A preferred embodiment of the mutuant a-amylase according to the invention is characterized by the fact that one or both of the methionine amino acid residues in positions 200 and 206 in B. stearothermophiius a-amylase or the methionine amino acid residues in homologous positions in other a-amylases are exchanged. In relation to positions 200 and 206 in B. stearotherrnophilus a-amylase the homologous position in B. licheniforniis a-amylase is 197 and the homologous position in B. amyloliquefaciens a-amylase is position 197.
Experimentally it has been found that these mutants exhibit both an improved activity level and an improved stability in the presence of the oxidizing agents.
As illustrated in Example 2, 3 and 4 below, the preferred a-amylase was observed to exhibit a poor level of cleaning performance in a wash liquor having a pH of 10 or greater both in the presence and in the absence of an organic peroxy acid bleach (e. g., PAP). Thus, the improved bleach stability of the above described a-amylases gave little benefit in cleaning performance when the amylases are formulated in machine dishwashing compositions at pH levels greater than or equal to 14.
In order to obtain improved levels of starch removal with a detergent formulation containing a-amylases which are bleach resistant, it was observed that the pH of the wash liquor must be below 10, preferably 6 to 9.5, most preferably 7 to 9.5. (See Examples 5 and 6). As noted above, at a reduced alkalinity of less than pH 10, traditional peroxygen bleaching agents do not deliver a significant bleaching benefit.
Therefore, according to the invention the above described a-amylases must be formulated with an organic peroxy acid in a detergent composition, provided that a 1% aqueous solution of the detergent composition has a pH of from 6 to 9, to provide overall effective performance on both starch and tannin.
hetergent Builder Materials The compositions of this invention can contain all manner of detergent builders commonly taught for use in machine dishwashing or other cleaning compositions. The builders can 5 include any of the conventional inorganic and organic water-soluble builder salts, or mixtures thereof and may comprise 1 to 75%, and preferably, from about 5 to about 70%
by weight of the cleaning composition, 10 Typical examples of phosphorus-containing inorganic builders, when present, include the water-soluble salts, especially alkali metal pyrophosphates, orthophosphates and polyphosphates. Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, pyrophosphates and hexametaphosphates.
Suitable examples of non-phosphorus-containing inorganic builders, when present, include water-soluble alkali metal carbonates, bicarbonates, sesquicarbonates, borates, silicates, metasilicates, and crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite seeds), potassium carbonate, sodium and potassium bicarbonates, silicates and zeolites.
Particularly preferred inorganic builders can be selected from the group consisting of sodium tripolyphosphate, potassium tripolyphosphate, potassium pyrophosphate, sodium, carbonate, potassium carbonate, sodium bicarbonate, sodium silicate and mixtures thereof, When present in these compositions, sodium tripolyphosphate concentrations will range from about 2% to about 40%; preferably from 5% to 30%.
Potassium tripolyphosphate concentrations will range from about 2% to about 50%, preferably from 5% to 40%. Sodium and potassium carbonate and bicarbonate when present can range from about 5% to about 50%; preferably from 10% to 30% by weight of the cleaning compositions. Sodium tripolyphosphate, potassium tripolyphosphate and potassium pyrophosphate can be used as builders in gel forntulations, where they may be present from 3 to 50%, preferably from 10 to 40%.
Organic detergent builders can also be used in the present invention. Examples of organic builders include alkali metal citrates, succinates, malonates, fatty acid sulfonates, fatty acid carboxylates, nitrilotriacetates, phytates, phosphonates, alkanehydroxyphosphonates, oxydisuccinates, alkyl and alkenyl disuccinates, oxydiacetates, carboxymethyloxy succinates, ethylenediaaaine tetraacetates, tartrate monosuccinates, tartrate disuccinates, tartrate monoacetates, tartrate diacetates, oxidized starches, oxidized heteropolymeric polysaccharides, polyhydroxysulfonates, polycarboxylates such as polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/ polymethacrylate copolymers, acrylate/
maleate/vinyl alcohol terpolymers, aminopolycarboxylates and polyacetal carboxylates, and polyaspartates and mixtures thereof. Such carboxylates are described in US-A-4,144,226, US-A-4,146,495 and US-A-4,686,062.
Alkali metal citrates, nitrilotriacetates, oxydisuccinates, polyphosphonates and acrylate/maleate copolymers and .
acrylate/maleate/vinyl alcohol terpolymers are especially preferred organic builders. When present they are preferably available from 1% to 35% of the total weight of the detergent compositions.
The foregoing detergent builders are meant to illustrate but not limit the types of builders that can be employed in the present invention.
The composition may also include an enzyme selected from the group consisting of a protease and a lipase in an effective amount to remove soils.
Anti-Scalant Scale formation on dishes and machine parts is an important problem that needs to be resolved or at least mitigated in formulating a machine warewashing product, especially in the case of low-phosphate (e.g. less than the equivalent of 20%
by weight, particularly 10°s by weight of sodium triphosphate) and phosphate-free machine warewashing compositions, particularly zero-P machine warewashing compositions.
In order to reduce this problem, co-builders, such as polyacrylic acids or polyacrylates (PAA), acrylate/maleate copolymers, and the various organic polyphosphonates, e.g. of the Dequest~" range, may be incorporated in one or more system components. For improved biodegradability, the block co-polymers of formula (I) as defined in WO-94/17170 may also be used. In any component, the amount of co-builder may be in the range of from 0.5 to 10, preferably from 0.5 to 5, and more preferably from 1 to 5°s by weight.
Surfactants Useful surfactants include anionic, nonionic, cationic, amphoteric, zwitterionic types and mixtures of these surface active agents. Such surfactants are well known in the .
detergent art and are described at length in "Surface Active Agents and Detergents", Vol. II, by Schwartz, Perry & Hirch, Interscience Publishers, Inc. 19591 Preferred surfactants are one or a mixture of:
Anionic surfactants Anionic synthetic detergents can be broadly described as surface active compounds with one or more negatively charged functional groups. An important class of anionic compounds are the water-soluble salts, particularly the alkali metal - salts, of organic sulfur reaction products having in their molecular structure an alkyl radical containing from about 6 to 24 carbon atoms and a radical selected from the group consisting of sulfonic and sulfuric acid ester radicals.
Primary A11cy1 Su1 fa tes Rl OSO~NI
where R' is a primary alkyl group of 8 to 18 carbon atoms and M is a solubilizing ration. The alkyl group R' may have a mixture of chain lengths. It is preferred that at least two thirds of the R' alkyl groups have a chain length of 8 to 14 carbon atoms. This will be the case if R1 is coconut alkyl, for example. The solubilizing ration may be a range of rations which are in general monovalent and confer water solubility. Alkali metal, notably sodium, is especially envisaged. Other possibilities are ammonium and substituted ammonium ions, such as trialkanol- or trialkyl-ammonium.
AIhy1 Ether Sulfates 2 0 RIO (CHaCH20) nSO~?
where R' is a primary alkyl group of 8 to 18 carbon atoms, n has an average value in the range from Z to 6 and M is a solubilizing ration. The alkyl group RI may have a mixture of chain lengths. It is preferred that at least two thirds of the RI alkyl groups have a chain length of 8 to 14 carbon atoms. This will be the case if RI is coconut alkyl, for example. Preferably n has an average value of 2 to 5.
Fatty Aci d Ester Sulfonates 3 0 RICH (S03M) CO~
where RZ.is an alkyl group of 6 to 16 atoms, R3 is an alkyl group of 1 to 4 carbon atoms and M is a solubilizing ration.
The group RZ may have a mixture of chain lengths. Preferably at least two thirds of these groups have 6 to 12 carbon WO 97/I$287 PCT/EP96/04659 atoms. This will be the case when the moiety RzCH(-)COZ(-) is -derived from a coconut source, for instance. It is preferred that .R3 is a straight chain alkyl, notably methyl or ethyl.
-AlJcy1 Benzene Sulfonates R'~ArS03hl where R4 is an alkyl group of 8 to 18 carbon atoms, Ar is a benzene ring (C6FI4) and M is a solubilizing cation. The group R'~ may be a mixture of chain lengths. Straight chains of 11 to 14 carbon atoms are preferred.
Organic phosphate based anionic surfactants include organic phosphate esters such as complex mono- or diester phosphates of hydroxyl- terminated alkoxide condensates, or salts thereof. Included in the organic phosphate esters are phosphate ester derivatives of polyoxyalkylated alkylaryl phosphate esters, of ethoxylated linear alcohols and ethoxylates of phenol. Also included are nonionic alkoxylates having a sodium alkylenecarboxylate moiety linked to a terminal hydroxyl group of the nonionic through an ether bond. Counterions to the salts of all the foregoing may be those of alkali metal, alkaline earth metal, ammonium, alkanolammonium and alkylammonium types.
Particularly preferred anionic surfactants are the fatty acid ester sulfonates with formula:
RzCH (SO3M) CO~
where the moiety RaCH(-) COa (-) is derived from a coconut source and R3 is either methyl or ethyl.
' Nonionic surfactants Nonionic surfactants can be broadly defined as surface active compounds with one or more uncharged hydrophilic substituents. A major class of nonionic surfactants are those compounds produced by the condensation of alkylene oxide groups with an organic hydrophobic material which may - be aliphatic or alkyl aromatic in nature. The length of the hydrophilic or polyoxyalkylene radical which is condensed 5 with any, particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
Illustrative, but not limiting examples, of various suitable nonionic surfactant types are:
polyoxyethylene or polyoxypropylene condensates of aliphatic carboxylic acids, whether linear- or branched-chain and unsaturated or saturated, containing from about 8 to about 18 carbon atoms in the aliphatic chain and incorporating from about 2 to about 50 ethylene oxide and/or propylene oxide units. Suitable carboxylic acids include "coconut" fatty acids (derived from coconut oil) which contain an average of about 12 carbon atoms, "tallow" fatty acids (derived from tallow-class fats) which contain an average of about 18 carbon atoms, palmitic acid, myristic acid, stearic acid and lauric acid, polyoxyethylene or polyoxypropylene condensates of aliphatic aleohols, whether linear- or branched-chain and unsaturated or saturated, containing from about 6 to about 24 carbon atoms and incorporating from about 2 to about 50 ethylene oxide and/or propylene oxide units. Suitable alcohols include "coconut" fatty alcohol, "tallow" fatty alcohol, lauryl alcohol, myristyl alcohol and oleyl alcohol.
Ethoxylated fatty alcohols may be used alone or in admixture - with anionic surfactants, especially the preferred surfactants above. The average chain lengths of the alkyl group Rs in the general formula:
RSO (CH2CHa0) nH
is from 6 to 20 carbon atoms. Notably the group RS may have chain lengths in a range from 9 to 18 carbon atoms. _ The average value of n should be at least 2. The numbers of ethylene oxide residues may be a statistical distribution around the average value. However, as is known, the distribution can be affected by the manufacturing process or altered by fractionation after ethoxylation. Particularly preferred ethoxylated fatty alcohols have a group RS which has 9 to 18 carbon atoms while n is from 2 to 8.
Also included within this category are nonionic surfactants having a formula:
Rd-(CH2CHU),~(CHsCH20)y(CIi~CHt~~yH
l~t~ Rs wherein R6 is a linear alkyl hydrocarbon radical having an average of 6 to 18 carbon atoms, R' and R$ are each linear alkyl hydrocarbons of about 1 to about 4 carbon atoms, x is an integer of from 1 to 6, y is an integer of from 4 to 20 ~.nd z is an integer from 4 to 25.
A preferred nonionic surfactant of the above formula is Poly-Tergent SLF-18' a registered trademark of the Olin Corporation, New Haven, Conn. having a composition of the above formula where R6 is a C6-Clo linear alkyl mixture, R' and Rg are methyl, x averages 3, y averages 12 and z averages 16.
Another preferred nonionic surfactant is WO 97!18287 PCT/EP96/04659 R90 {CHsCHQ) j{CHsCH2U)k{CHy CH{dH}R1o)1 I
CHI
wherein R9 is a linear, aliphatic hydrocarbon radical having from about 4 to about 18 carbon atoms including mixtures thereof; and R1° is a linear, aliphatic hydrocarbon radical having from about 2 to about 26 carbon atoms including mixtures thereof; j is an integer having a value of from 1 to about 3; k is an integer having a value from 5 to about 30;
and z is an integer having a value of from 1 to about 3.
Most preferred are compositons in which j is 1, k is from about 10 to about 20 and 1 is 1. These surfactants are described in WO-94/22800. Other preferred nonionic surfactants are linear fatty alcohol alkoxylates with a capped terminal group, as described in US-A-4,340,766.
Particularly preferred is Plurafac LF403 ex. BASF.
polyoxye~thylene or polyoxypropylene condensates of alkyl phenols, whether linear- or branched-chain and unsaturated or saturated,containing from about 6 to 12 carbon atoms and incorporating from about 2 to about 25 moles of ethylene oxide and/or propylene oxide.
polyoxyethylene derivatives of sorbitan mono-, d3-, and tri-fatty acid esters wherein the fatty acid component has between 12 and 24 carbon atoms. The preferred polyoxyethylene derivatives are of sorbitan monolaurate, sorbitan trilaurate, sorbitan monopalmitate, sorbitan tripalmitate, sorbitan monostearate, sorbitan ~monoisos.tearate, sorbitan tripalmitate, sorbital tristearate, t sorbitan monooleate, and sorbitan trioleate. The polyoxyethylene chains may contain between about 4 and 30 ethylene oxide units, preferably about 10 to 20. The sorbitan ester derivatives contain 1, 2 or 3 polyoxyethylene chains dependent upon whether they are mono-, di- or tri-acid esters.
polyoxyethylene-polyoxypropylene block copolymers having formula:
HO ( CHaCHaO ) , ( CH ( CH3 ) CH~O ) b ( CH2CHa0 ) ~H
or HO ( CH ( CH3 ) CHaO ) d ( CH2CHa0 ) ~ ( CH ( CH3 ) CHZO ) fFi to wherein a, b, c, d, a and f are integers from 1 to 350 reflecting the respective polyethylene oxide and poly-propylene oxide blocks of said polymer. The polyoxyethylene component of the block polymer constitutes at least about 10~
of the block polymer. The material preferably has a molecular weight of between about 1,000 and 15,000, more preferably from about 1,500 to about 6,000_ These materials are well-known in the art. They are available under the trademark "Pluronic" and "Pluronic R", a product of BASF Corporation.
Amine oxides having formula:
Ri2RisRi4N=O
wherein R12, Rts and Rt4 are saturated aliphatic radicals or substituted saturated aliphatic radicals. Preferable amine oxides are those wherein R'2 is an alkyl chain of about 10 to about 20 carbon atoms and R13 and R14 are methyl or ethyl groups or both R12 and RI3 are alkyl chains of about 6 to about 14 carbon atoms and R14 is a methyl or ethyl group_ .Amphoteric synthetic detergents can be broadly described as derivatives of aliphatic and tertiary amines, in which the aliphatic radical may be straight chain or branched and wherein one of the aliphatic substituents contain from about 8 to about 18 carbons and one contains an anionic water-solubilizing group, i.e., carboxy, sulpho, sulphato, phosphato or phosphono. Examples of compounds falling within this definition are sodium 3-dodecylamino propionate and sodium 2-dodecylamino propane sulfonate.
Zwitterionic synthetic detergents can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium and sulphonium compounds in which the aliphatic radical may be straight chained or branched, and wherein one of the aliphatic substituents contains from about 8 to about 18 carbon atoms and one contains an anionic water-solubilizing group, e.g., carboxy, sulpho, sulphato, phosphato or phosphono. These compounds are frequently referred to as betaines. Besides alkyl betaines, alkyl amino and alkyl amido betaines are encompassed within this invention.
AIIzy1 Glycosides l2rSG (R16O) " ~ZI ) p wherein Ris is a monovalent organic radical (e.g., a monovalent saturated aliphatic, unsaturated aliphatic or aromatic radical such as alkyl, hydroxyalkyl, alkenyl, hydroxyalkenyl, aryl, alkylaryl, hydroxyalkylaryl, arylalkyl, alkenylaryl, arylalkenyl, etc.) containing from about 6 to about 30 (preferably from about 8 to 18 and more preferably from about 9 to about 13) carbon atoms; R'6 is a divalent hydrocarbon radical containing from 2 to about 4 carbon atoms such as ethylene, propylene or butylene (most preferably the unit (Rr60)n represents repeating units of ethylene oxide, propylene oxide and/or random or block combinations thereof);
n is a number having an average value of from 0 to about 12;
ZI represents a moiety derived from a reducing saccharide containing 5 or 6 carbon atoms (most preferably a glucose unit); and p is a number having an average value of from 0.5 to about 10 preferably from about 0.5 to about 5 .
Examples of commercially available materials from Her~lcel Kommanditgesellschaft Alctien of Dusseldorf, Germany include APG° 300, 325 and 350 with R15 being C9-C11, n is 0 and p is 1.3, 1.6 and 1.8-2.2 respectively; APG° 500 and 550 with Rls 5 is C12-C13, n is 0 and p is 1.3 and 1.8-2.2, respectively; and APG° 600 with Rls being CIa-C14, n is 0 and p is 1.3.
While esters of glucose are contemplated especially, it is envisaged that corresponding materials based on other 10 reducing sugars, such as galactose and mannose are also suitable.
Particularly preferred anionic surfactants are the fatty acid ester sulfonates with formula:
15 RICH (S03M) CO~
where the moiety RZCH(-) COa (-) is derived from a coconut source and .R~ is either methyl or ethyl.
The amount of glycoside surfactant, anionic surfactant 20 andJor ethoxylated fatty alcohol surfactant will be from 0.5 to 40~ by weight of the composition. Desirably the total amount of surfactant lies in the same range. The preferred range of surfactant is from 0.5 to 30~ by weight, more preferably from 0.5 to 15~ by weight.
ill r An inert particulate filler material which is water-soluble may also be present in cleaning compositions. This material should not precipitate calcium or magnesium ions at the filler use level. Suitable for this purpose are organic or inorganic compounds. Organic fillers include sucrose esters and urea. Representative inorganic fillers include sodium sulfate, sodium chloride and potassium chloride. A preferred filler is sodium sulfate. Its concentration may range from 0% to 60%, preferably from about 5% to about 30% by weight of the cleaning composition.
Thickeners and Stabilizers Thickeners are often desirable for liquid cleaning compositions. Thixotropic thickeners such as smectite clays including montmorillonite (bentonite), hectorite, saponite, and the like may be used to impart viscosity to liquid cleaning compositions. Silica, silica gel, and alumino-l0 silicate may also be used as thickeners. Salts of polyacrylic acid (of molecular weight of fr~a about 300, 000 up to 6 million and higher), including polymers which are cross-linked may also be used alone or in combination with other thickeners. Use of clay thickeners for machine dishwashing compositions is disclosed for example in US-A-4,431,559; US-A-4,511,487; US-A-4,740,327; US-A-4,752,409.
Commercially available synthetic smectite clays include Laponite supplied by Laporte Industries. Commercially available bentonite clays include Korthix Hue' and VWH ex Combustion Engineering, Inc.; Polargel T'" ex American Colloid'.
Co.; and Gelwhite'" clays (particularly Gelwhite GP and H) ex English China Clay Co. Polargel T is preferred as imparting a more intense white appearance to the composition than other clays. The amount of clay thickener employed in the compositions is from 0.1 to 10%, preferably 0.5 to 5%. Use of salts of polymeric carboxylic acids is disclosed for example in GH-A-2,164,350A, US-A-4,859,358 and US-A-4,836,948.
For liquid formulations with a 'gel" appearance and rheology, particularly if a clear gel is desired, a chlorine-resistant polymeric thickener is particularly useful. USA-4,260,528 discloses natural gums and resins for use in clear machine dishwashing detergents, which are not chlorine stable. Acrylic acid polymers that are cross-linked WO 97/18287 PCTIEP96lOd659 manufactured by, for example, B.F. Goodrich and sold under the trade name "Carbopol" have been found to be effective for production of clear gels, and Carbopol 940, 617 and 627, having a molecular weight of about 4,000,000 are particularly preferred for maintaining high viscosity with excellent chlorine stability over extended periods. Further suitable chlorine-resistant polymeric thickeners are described in US-A-4,867,896. The amount of thickener employed in the compositions is from 0 to 5%, preferably 0.5-3%.
i Stabilizers and/or co-structuraats such as long=chain calcium and sodium soaps and C~x to Cls sulfates are detailed in US-A-3,956,158 and US-A-4,271,030 and the use of other metal salts of long-chain soaps is detailed in US-A-4,~~2,409o Qther co-structurants include Laponite and metal oxides and their salts as described in US-A-4,933,101. The amount of stabilizer which may be used in the liquid cleaning compositions is from 0.01 to 5% by weight of the composition, preferably 0.01-2%. Such stabilizers are optional in gel formulations. Co-structurants which are found especially suitable for gels include trivalent metal ions at 0.01-4% of the compositions, Laponite and/or water-soluble structuring chelants at 0.01-5%. These co-structurants are more fully described in US-A-5,141,664.
Anti-TarnishinoLAqents Anti-tarnishing agents may be incorporated into the compositions. Such agents include benzotriazole, certain 1,3 N-azoles described in US-A-5,480,576; isocyanuric acid described in US-A-5,374,369; and purine compounds described in US-A-5,468,410.
Defoamer The formulations of the cleaning composition comprising surfactant may further include a defoamer. Suitable defoamers include mono-and distearyl acid phosphate, silicone oil and mineral oil. Even if the cleaning composition has only defoaming surfactant, the defoamer assists to minimize foam which food soils can generate. The compositions may include 0.02 to 2% by weight of defoamer, or preferably 0.05-1.0%.
Optional Ingredients Minor amounts of various other components may be present in the cleaning composition. These include bleach scavengers including but not limited to sodium bisulfate, sodium perborate, reducing sugars, and short chain alcohols;
solvents and hydrotropes such as ethanol, isopropanol and xylene sulfonates; flow control agents (in granular forms);
enzyme stabilizing agents; soil suspending agents;
antiredeposition agents; anti-corrosion agents; ingredients ~~ enhance decor care such as certain aluminum salts described in WO-96/36687 and US-A-5624892; colorants;
perfumes; and other functional additives.
The following examples will serve to distinguish this invention from the prior art and illustrate its embodiments more fully. Unless otherwise indicated, all parts, percentages and proportions referred to are by weights.
The half-lives of amylases were determined by the method in the specification. Thus, the amylase, at a level of 4x10'mu/1, was incubated at 55°C in a solution containing 2mM
sodium citrate, 1mM sodium citrate, 1mM epsilon phthalimidoperoxyhexanoic acid and 36 ppm hardness ions with a calcium to magnesium ratio of 4:1 and maintained at pH 8Ø
Samples were withdrawn at suitable intervals and analyzed for enzyme activity on a Roche Cobas Fara Analyzer using Roche S Reagent. This contains p-nitrophenyl-a-D-maltoheptaoside as the substrate which is hydrolyzed by the amylase in question to give p-nitrophenylmaltotriose. This moiety is then hydrolyzed by glycoamylase to p-nitrophenylmaltotriose, which in turn is hydrolyzed by gluco amylase to p-nitrophenyl glycoside aad further hydrolyzed by a-glucosideose to p-nitrophenol. The absorbance of p-nitrophenol is measured at 405nm.
The results for Termanyl°", Duramyl'" and Purafect ~ OxAm 4000 G
(ex. Genencor) are given in Table 1.
Termamyl Duramyl Purafect~ OxAm <1 13 >20 Thus, Termamyl is outside the scope of the invention.
EXAMPhE 2 The amylolytic activity and starch removal performance of a bleach resistant a-amylase (Duramyl~", supplied by Novo) was compared to that of~a conventional amylase (i.e. Termamyl, supplied by Novo) under model wash conditions in a beaker at pH 10, 55°C.
Two detergent compositions were prepared, including an amount of Duramyl'~ and Termanyl~' to provide an enzymatic activity level of 220 Maltose units per liter in the wash solution.
Also included in the compositions were 0.2g/1 sodium ' CA 02236881 2004-06-02 nitrilotriacetate and carbonate/bicarbonate buffer containing 1.7g/1 of NazC03.10Hs0 and 0.34g/1 of NaHC03. No bleaching agent was added to either sample. The pH of an aqueous solution of each of the compositons was adjusted to 5 pH 10 with NaOH or HzSO, as needed.
The amylolytic activity of the two types of enzyme was determined as follows:
Model wash solutions containing carbonate/bicarbonate buffer, 10 builder (if present) and hardness ions (if present) are ' stirred in a constant temperature jacketed beaker. Enzyme and bleach (if present) are added. Samples are withdrawn from this solution at fixed times and added to solid starch azure, a crystalline potato starch polymer linked with 15 Remazol"" Brilliant Blue. This.mixture is incubated for a set time, centrifuged and the color development in the supernatant measured. This experiment measures the change in enzyme activity over time.
Absorbance values were recorded over a 60 minute time period.
20 The greater the absorbance value, the higher the activity of the enzyme in the composition. The following results were obtained at pH 10.
Absorbaace at 59611m (or Amylase Activity) Elapsed time (min) Duramyl Termamyl _ ._._ ._ i 0 0.44 1.23 10 0.53 1.17 20 0.27 1.24 30 0.29 1.23 40 0.25 1.23 50 0.23 1.30 60 0.22 1.26 At pH 10, with no bleach present, the conventional amylase exhibited a significantly higher enzymatic activity than the composition containing the a-amylase of the present -invention.
The starch removal performance of the two samples was also compared in an industrial dishwasher by washing three racks of dishes, each rack being loaded with a range of dishware that included ten starch-soiled plates. The components of the cleaning composition were dosed into the machine just once, prior to washing the first rack of dishes. Since there was no further dosing of product, each successive wash resulted in a 10~ dilution of the product concentration due to the introduction of fresh rinse water at the end of each main wash. There was a waiting period of 5 minutes between the processing of the second and third racks of dishes. The level of residual starch was assessed visually after disclosure of the washed plate in iodine solution.
SUBSTITUTE SHEET (RULE 26) Termamyl 300L and Duramyl 300L were each dosed to give 4 x 103 Mu/Q in the wash. The following results were obtained.
Residual Starch (~ Area ) Sample Rack 1 Rack 2 Rack 3 Termamyl 300L 13 13 12 Duramyl 300L 100 100 100 Consistent with the observed amylolytic activity profiles above, at a wash pH of 10 and in the absence of bleach, the composition containing the conventional amylase, Termamyl 300L, was observed to give significantly better starch removal performance than the novel a-amylase when both were incorporated in a detergent composition as described above.
FXaMT~T.F 3 The compositions of Example 2 were modified by incorporating hydrogen peroxide (100 ppm Av Ox) or hypochlorite (60 ppm Av.
Cl) as bleaching agent. Three racks of soiled dishware were washed as described in Example 2 and evaluated for residual starch soil with the following results.
SUBSTITUTE SHEET (RULE 26) WO 97/18287 PCT/EP96/a4659 Residual ' Starch ( ~SArea ) Bleach Eazyme Rack Raek 2 Rack Hypochlorite Termamyl 300L 100 100 100 Duramyl 300L 100 100 100 Hydrogen Termamyl 300L 7 8 10 Peroxide Duramyl 300L 100 100 100 Chlorine bleach has a devastating impact on the stability of both amylase variants and so the cleaning results are poor in both cases. There is a big improvement in enzyme stability rahen the bleach is hydrogen peroxide. However, the starch removal performance of both enzymes remained essentially unchanged relative to the composition with no bleach described in Example 2. Thus, a.n the presence of hydrogen peroxide at pH 10, it is the conventional amylase, not the bleach-resistant amylase that gives the better starch removal performance.
Epsilon-phthalimido peroxyhexanoic acid (PAP) and peracetic acid (PAA) were both used in lieu of the hydrogen peroxide as peroxygen bleaching agent in the sample of Example 2 containing the Duramyl a-amylase. The pH of the wash solution was adjusted to a value of 10. The starch removal performance of the composition containing Duramyl and these peracids was also observed after three washing cycles as described in Example 2. Residual starch levels were 70, 100 and 95~ respectively, when the bleaching agent was PAP, and were 15, 100 and 100 respectively when the bleaching agent was PAA.
Therefore, substituting the conventional oxygen bleaching agent, hydrogen peroxide, with a more powerful peracid bleaching agent (PAP or PAA) did not significantly improve the starch removal performance of the Duramyl cx-amylase when formulated in a detergent composition at pH 10, and therefore at this wash pH there is still no benefit for this novel cx-amylase over the conventional Termamyl amylase.
The amylolytic activity of both a bleach-resistant amylase and Termamyl were monitored at a wash pH of 8.5, both in the absence and presence of PAP. The technique used a.s the same as that described in Example 2. The relative amylase activities, based on absorbancies, are given in Table 6.
Relative Amylase Activity at pH
8.5 Elapsed Duramyl Duramyl Termamyl Termamyl 5 Time + PAP + PAP
(minutes) 0 1.25 2.5 0.75 0.75 5 1.0 2.4 1.0 0.5 10 1.0 2.25 1.0 0.8 15 0.85 1.7 1.0 0.2 10 20 0.90 1.25 1.0 0.2 30 1.0 1.0 1.0 0.2 Unexpectedly, the amylolytic activity of the formulation containing the a-amylase according to the invention was 15 synergistically enhanced by addition of the peracid at pH
8.5. In contrast, the activity of Termamyl decreased on addition of the PAP. This enhancement between the bleach-resistant amylase and PAP did not occur at pH 10, as seen from the absorbance data in Table 6.
SUBSTITUTE SHEET (RULE 26) RELATIVE AMYLASE
ACTIVITY AT
pH 3Ø0 Elapsed time Duramyl Duramyl + PAP
(minutes) 0 0.14 0.06 5 0.11 0.05 0.12 0.10 0.08 0.18 10 20 0.06 0.04 30 0.06 0.05 Again, this is surprising since one would have expected that as the pH moved down from pH 10 to pH 8.5, that is as 15 the pH moved to the range of greatest activity for PAP, the effect on Duramyl would be negative, not positive. Also, this positive synergistic benefit on the bleach-resistant amylase activity occurs at the pH region where the functionality of PAP (i.e. bleaching of tannin} is optimum.
The starch and tannin removal performance profiles were determined for a bleach-resistant a-amylase in combination with a wide range of peracid bleaching agents (i.e.
hydrophobic monoperoxy- and diperoxy-acids; hydrophilic monoperoxy acid; inorganic peroxyacid).
The cleaning experiments were conducted in a domestic dishwashing machine wherein the wash temperature was SUBSTITUTE SHEET (RULE 26) maintained at 55°C and the wash pH at 8.5 (with borate buffer) or 10 (with carbonate/bicarbonate buffer). In one type of experiment where only four times stained tea cups were included, the wash time was 30 seconds. In a second =teat, where a combination of soiled tea cups and starch soiled plates were included, the wash time was 2 minutes.
The results of these tests are given in Table 8.
30 second 2 minute wash wash PERACID Wash Residual Residual Residual pii Tea+ Tea+ Starch PAP 8.5 0 0 45 TPCAP* 8.5 0.7 0.8 39 DPDDA** 8.5 1.0 0_3 37 H48*** 8.5 2.4 1.5 26 H48 10 1.5 - -KMPS**** 8.5 2.9 2.0 34 KMPS 10 2.0 - -* N,N~-terephthaloyl-di (6-amino percaproic acid) ** 1,12-diperoxydodecanedioic acid *** magnesium monoperoxyphthalate **** potassium monopersulfate +The stained tea cups are rated on a zero (no residual stain) to five (heavy stain) scale. The difference between SUBSTITUTE SHEET (RULE 26) zero and non-zero tea scores is considered to be highly significant because any residual tea stain rapidly builds up during subsequent re-use and re-washing steps.
With regard to starch removal, the foregoing was designed to be a highly stressed performance test in order to clearly demonstrate differences. Differences in the starch removal scores for KMPS, DPDDA, TPCAP, PAP and H48 systems at pH 8.5 are considered to be small and all systems are capable of giving good levels of starch removal. However, there were significant differences in tannin removal. H48 and KMPS gave very poor levels of tannin removal at pH 8.5 and PAP was significantly better than both DPDDA and TPCAP.
Thus, the system that gives overall the best tannin and starch cleaning profile is the PAP/amylase system with the other hydrophobic peracid/enzyme combinations some distance behind.
2 0 E~CAMPLE 7 Surprisingly, it is found that the stability of Duramyl towards bleach is greatly enhanced when builder is present in the wash solution. A similar enhanced stability was not observed with Termamyl. The amyloyltic activity was monitored by the following method:
Starch azure, a crystalline potato starch polymer linked with Remazol Brilliant Blue, is heated in distilled water at 80°C for 15 minutes and transferred to glass slides (1 inch x 1 inch) which are then dried at room temperature overnight.
The slides are weighed. Model wash solutions containing pH
8.5 borate buffer, builder (at 0.56g/1 if present) and hardness ions (36ppm expressed as CaC03; 4:1 Ca:Mg ratio) are stirred and maintained at 55°C in a constant temperature jacketed beaker. Three retrograded starch slides are added , to the beaker, followed by either Duramyl or Ternaa.myl and then PAP (at 1mM). The absorbance of aliquots are measured , at 596 nm to give an assessment of in-wash enzyme activity.
In addition, at the end of the experiment, the slides are dried and weighed to determine the level of soil removal.
The builders evaluated were sodium nitrilotriacetate, sodium citrate and an acrylate/maleate/vinyl alcohol terpolymer from Huls, described in U.S_ 4,686,062. The activity of the enzymes was followed over a period of 30 minutes. The results are shown in Table 9.
Ingredients A B C D E F G H
NTA X J X X X J X X
5 Citrate X X ~ X X X J X
Huls X X X J X X X J
Polymer Duramyl J J J J X X X X
Termamyl X X X X J J J J
Time Residual (minutes) Amylolytic Activity 0 100 10 100 l0 100 10 10 100 J means present in the wash solution.
* X means absent from the wash solution.
Good stability of the bleach-resistant amylase in the presence of bleach is only obtained when builder is present SUBSTITUTE SHEET (RULE 26) in the wash solution (see B, C and D compared to A)_ A
similar enhancement of the stability of Termamyl, ~
traditional amylase, is not observed (see F, G, H compared to E) .
Using the same procedure outlined in Example 7, the effect of water hardness on the stability of a bleach-resistant amylase in the presence of 2mM NTA and 20 ppm Av Ox PAP was evaluated at 65°C. The activity of Duramyl was followed over 30 minutes. The results are shown in Table 10.
Table 10 Resish.al Amyl of y~ic Ac~iv3.tv Time Water Hardness (min.) (expressed as CaC03;
4:1 Ca: Mg ratio) i 0 ppm 10 ppm 36 ppm 80 ppm This demonstrates that hardness ions have a beneficial effect on the amylolytic stability of the bleach-resistant K
enzyme in the presence of builder and PAP.
SUBSTITUTE SHEET (RULE 26)
Claims (29)
1. A warewashing composition for a mechanical dishwashing machine comprising:
(a) an organic monoperoxy or diperoxy acid which exhibits maximum tannin stain removal efficacy at a wash pH of about 8.5 which is at or near the pKa of the peroxy acid the organic peroxy acid being present in an amount of 1 ppm to 100 ppm available O2 in the solution;
(b) an amylase enzyme which, when incubated at 55° C in a solution of 2 mM sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half-life of 10 minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405 nm of solution samples incubated with p-nitrophenyl-.alpha.-D-maltoheptaoside as substrate and gluco amylase and .alpha.-glucosidase as coupled enzymes; and (c) 1% by weight to 75% by weight of a builder, provided that a 1% aqueous solution of the warewashing composition has a pH of 6 to 9.5.
(a) an organic monoperoxy or diperoxy acid which exhibits maximum tannin stain removal efficacy at a wash pH of about 8.5 which is at or near the pKa of the peroxy acid the organic peroxy acid being present in an amount of 1 ppm to 100 ppm available O2 in the solution;
(b) an amylase enzyme which, when incubated at 55° C in a solution of 2 mM sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half-life of 10 minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405 nm of solution samples incubated with p-nitrophenyl-.alpha.-D-maltoheptaoside as substrate and gluco amylase and .alpha.-glucosidase as coupled enzymes; and (c) 1% by weight to 75% by weight of a builder, provided that a 1% aqueous solution of the warewashing composition has a pH of 6 to 9.5.
2. A composition according to claim 1 wherein the organic mono peroxy acid is selected from a group consisting of a peroxy benzoic acid, an aryl substituted peroxy benzoic acid, an aliphatic monoperoxy acid, a substituted aliphatic monoperoxy acid and mixtures thereof.
3. A composition according to claim 2 wherein the aliphatic monoperoxy acid is selected from the group of epsilon-phthalimidoperoxyhexanoic acid (PAP), o-carboxybenzamidoperoxyhexanic acid, N-nonenylamidoperadipic acid, N-noneylaminopersuccinic acid and mixtures thereof.
4. A composition according to claim 1 wherein the diperoxy acid is selected from the group consisting of 1,12-diperoxydodecanedioic acid; 1,9-diperoxyazelaic acid; diperoxybrassylic acid; diperoxysebacic acid; diperoxy-isophthalic acid; 2-decyldiperoxybutane-1,4-dioic acid and N,N'-terephthaloyl-di (6-aminopercaproic acid).
5. A composition according to claim 1 wherein the organic peroxy acid is encapsulated in a paraffin wax coating having a melting point from about 40°
C to about 50° C.
C to about 50° C.
6. A composition according to claim 1 wherein the .alpha.-amylase enzyme is Bacillus .alpha.-amylase.
7. A composition according to claim 1 wherein the .alpha.-amylase enzyme has one or more of its methionine amino acid residues exchanged for any amino acid residue except for cysteine and methionine.
8. A composition according to claim 1 wherein the builder is selected from the group consisting of inorganic water soluble builder salts, organic water soluble builder salts and mixtures thereof.
9. A composition according to claim 8 wherein the organic water soluble builder salt is selected from the group consisting of alkali metal citrates, succinates, malonates, fatty acid sulfonates, fatty acid carboxylates, nitrilotriacetates, phytates, phosphonates, alkanehydroxyphosphonates, oxydisuccinates, alkyl and alkenyl disuccinates, oxydiacetates, carboxymethyloxy succinates, ethylenediamine tetraacetates, tartrate monosuccinates, tartrate disuccinates, tartrate monoacetates, tartrate diacetates, oxidized starches, oxidized heteropolymeric polysaccharides, polyhydroxysulfonates, polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/polymethacrylate copolymers, acrylate/maleate/vinyl alcohol terpolymers, aminopolycarboxylates, polyacetal carboxylates and polyaspartates, and mixtures thereof.
10. A composition according to claim 9 wherein the builder is present in the amount of 1 to 40% by weight.
11. A composition according to claim 10 further comprising an enzyme selected from the group consisting of a protease and a lipase in an effective amount to remove soils.
12. A composition according to claim 11 further comprising an anti-tarnishing agent selected from the group consisting of a purine, a 1,3-N
azole, a cyanuric acid and mixtures thereof in an effective amount to prevent tarnishing.
azole, a cyanuric acid and mixtures thereof in an effective amount to prevent tarnishing.
13. A composition according to claim 12 wherein the anti-tarnish agent is benzotriazole.
14. A composition according to claim 1 wherein the pH of the aqueous solution is 6 to 9.
15. A composition according to claim 1 wherein wash water into which the composition is dosed has a water hardness of greater than 10 ppm expressed as calcium carbonate.
16. A method of cleaning dishware in a machine dishwashing machine comprising:
(a) applying an effective amount of a detergent composition comprising:
(i) an amylase enzyme which, when incubated at 55° C in a solution of 2 mM sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half-life of 10 minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405 nm of solution samples incubated with p-nitrophenyl .alpha.-D-maltoheptaoside as substrate and gluco amylase and .alpha.-glucosidase as coupled enzymes;
(ii) an organic monoperoxy or diperoxy acid which exhibits maximum tannin stain removal efficacy at a wash pH of about 8.5,which is at or near the pKa of the peroxy acid, the organic peroxy acid being present in an amount of 1 ppm to 100 ppm available O2 in the solution; and (iii) 1% by weight to 75% by weight of a builder, provided that a 1% aqueous solution of the warewashing composition has a pH of 6 to 9.5, and (b) rinsing the detergent composition from the cleaned dishware to substantially provide clean dishes.
(a) applying an effective amount of a detergent composition comprising:
(i) an amylase enzyme which, when incubated at 55° C in a solution of 2 mM sodium citrate, 1 mM epsilon phthalimidoperoxyhexanoic acid in 36 ppm water at pH 8.0, has a half-life of 10 minutes or greater based on an activity vs. time plot obtained via monitoring color development at 405 nm of solution samples incubated with p-nitrophenyl .alpha.-D-maltoheptaoside as substrate and gluco amylase and .alpha.-glucosidase as coupled enzymes;
(ii) an organic monoperoxy or diperoxy acid which exhibits maximum tannin stain removal efficacy at a wash pH of about 8.5,which is at or near the pKa of the peroxy acid, the organic peroxy acid being present in an amount of 1 ppm to 100 ppm available O2 in the solution; and (iii) 1% by weight to 75% by weight of a builder, provided that a 1% aqueous solution of the warewashing composition has a pH of 6 to 9.5, and (b) rinsing the detergent composition from the cleaned dishware to substantially provide clean dishes.
17. A method according to claim 16 wherein the organic mono peroxy acid is selected from a group consisting of a peroxy benzoic acid, an aryl substituted peroxy benzoic acid, an aliphatic monoperoxy acid, a substituted aliphatic monoperoxy acid and mixtures thereof.
18. A method according to claim 17 wherein the aliphatic monoperoxy acid is selected from the group of epsilon-phthalimidoperoxyhexanoic acid (PAP), o-carboxybenzamidoperoxyhexanoic acid, acid N-nonenylamidoperadipic acid, N-nonenylaminopersuccinic acid and mixtures thereof.
19. A method according to claim 16 wherein the diperoxy acid is selected from the group consisting of 1,12-diperoxydodecanedioic acid; 1,9-diperoxyazelaic acid; diperoxybrassylic acid; diperoxysbacic acid; diperoxy-isophthalic acid; 2-decyldiperoxybutane- 1,4-dioic acid and N,N'-terephthaloyl -di(6-aminopercaproic acid).
20. A method according to claim 16 wherein the organic peroxy acid is encapsulated in a paraffin wax coating having a melting point from about 40°
C to about 50° C.
C to about 50° C.
21. A method according to claim 16 wherein the .alpha.-amylase enzyme is Bacillus .alpha.-amylase.
22. A method according to claim 16 wherein the .alpha.-amylase enzyme has one or more of its methionine amino acid residues exchanged for any amino acid residue except for cysteine and methionine.
23. A method according to claim 16 wherein the builder is selected from the group consisting of inorganic water soluble builder salts, organic water soluble builder salts and mixtures thereof.
24. A method according to claim 23 wherein the organic water soluble builder salt is selected from the group consisting of alkali metal citrates, succinates, malonates, fatty acid sulfonates, fatty acid carboxylates, nitrilotriacetates, phytates, phosphonates, alkanehydroxyphosphonates, oxydisuccinates, alkyl and alkenyl disuccinates, oxydiacetates, carboxymethyloxy succinates, ethylenediamine tetraacetates, tartrate monosuccinates, tartrate disuccinates, tartrate monoacetates, tartrate diacetates, oxidized starches, oxidized heteropolymeric polysaccharides, polyhydroxysulfonates, polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/polymethacrylate copolymers, acrylate/maleate/vinyl alcohol terpolymers, aminopolycarboxylates, polyacetal carboxylates and polyaspartates, and mixtures thereof.
25. A method according to claim 16 wherein the builder is present in the amount of 1 to 40% by weight.
26. A method according to claim 16 further comprising an enzyme selected from the group consisting of a protease and a lipase in an effective amount to remove soils.
27. A method according to claim 16 further comprising an anti-tarnishing agent selected from the group consisting of a purine, a 1,3-N azole, a cyanuric acid and mixtures thereof in an effective amount to prevent tarnishing.
28. A method according to claim 27 wherein the anti-tarnish agent is benzotriazole.
29. A method according to claim 16 wherein the detergent composition is dosed into a wash water having a hardness of greater than 10 ppm expressed as calcium carbonate.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/558994 | 1995-11-16 | ||
| US08/558,994 US5741767A (en) | 1995-11-16 | 1995-11-16 | Peracid based dishwashing detergent composition |
| PCT/EP1996/004659 WO1997018287A1 (en) | 1995-11-16 | 1996-10-23 | A peracid based dishwashing detergent composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2236881A1 CA2236881A1 (en) | 1997-05-22 |
| CA2236881C true CA2236881C (en) | 2006-02-14 |
Family
ID=35892334
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002236881A Expired - Fee Related CA2236881C (en) | 1995-11-16 | 1996-10-23 | A peracid based dishwashing detergent composition |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2236881C (en) |
-
1996
- 1996-10-23 CA CA002236881A patent/CA2236881C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2236881A1 (en) | 1997-05-22 |
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