EP0518720A1 - Nonaqueous liquid automatic dishwashing composition containing enzymes - Google Patents

Nonaqueous liquid automatic dishwashing composition containing enzymes

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Publication number
EP0518720A1
EP0518720A1 EP19920401478 EP92401478A EP0518720A1 EP 0518720 A1 EP0518720 A1 EP 0518720A1 EP 19920401478 EP19920401478 EP 19920401478 EP 92401478 A EP92401478 A EP 92401478A EP 0518720 A1 EP0518720 A1 EP 0518720A1
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weight
percent
detergent
preferably
composition
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EP19920401478
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German (de)
French (fr)
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EP0518720B1 (en )
Inventor
Fahim U. Ahmed
Patrick Durbut
Julien Drapier
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Colgate-Palmolive Co
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Colgate-Palmolive Co
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL AND VEGETABLE OILS, FATS, FATTY SUBSTANCES AND WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials characterised by their shape or physical properties
    • C11D17/0004Non aqueous liquid compositions comprising insoluble particles
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL AND VEGETABLE OILS, FATS, FATTY SUBSTANCES AND WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/08Silicates
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL AND VEGETABLE OILS, FATS, FATTY SUBSTANCES AND WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease, amylase
    • C11D3/38618Protease or amylase in liquid compositions only
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL AND VEGETABLE OILS, FATS, FATTY SUBSTANCES AND WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease, amylase
    • C11D3/38627Preparations containing enzymes, e.g. protease, amylase containing lipase

Abstract

1. A nonaqueous liquid dishwashing composition comprising in percent by weight :

Description

    BACKGROUND OF THE INVENTION
  • [0001]
    It has been found to be very useful to have enzymes in dishwashing detergent compositions because enzymes are very effective in removing food soils from the surface of glasses, dishes, pots, pans and eating utensils. The enzymes attack these materials while other components of the detergent will effect other aspects of the cleaning action. However, in order for the enzymes to be highly effective, the composition must be chemically stable, and it must maintain an effective activity at the operating temperature of the automatic dishwasher. Chemical stability is the property whereby the detergent composition containing enzymes does not undergo any significant degradation during storage. This is also known as shelf life. Activity is the property of maintaining enzyme activity during usage. From the time that a detergent is packaged until it is used by the customer, it must remain stable. Furthermore, during customer usage of the dishwashing detergent, it must retain its activity. Unless the enzymes in the detergent are maintained in a suitable environment, the enzymes will suffer a degradation during storage which will result in a product that will have a decreased initial activity. When enzymes are a part of the detergent composition, it has been found that the initial free water content of the composition should be as low a level as possible, and this low water content must be maintained during storage, since water will activate the enzymes. This activation will cause a decrease in the initial activity of the detergent composition.
  • [0002]
    After the detergent container is opened, the detergent will be exposed to the environment which contains moisture. During each instance that the detergent is exposed to the environment it could possibly absorb some moisture. This absorption occurs by components of the detergent composition absorbing moisture, when in contact with the atmosphere. This effect is increased as the container is emptied since there will be a greater volume of air in contact with the detergent, and thus more available moisture to be absorbed by the detergent composition. This will usually accelerate the decrease in the activity of the detergent composition. The most efficient way to prevent a significant decrease in this activity is to start with an initial high activity of enzyme and to use components in the dishwashing composition which have a low hygroscopicity and a low alkalinity which will minimize any losses in activity as the detergent is being stored or used.
  • [0003]
    The stability of enzymes in a nonaqueous liquid detergent can be improved by using an alkali metal silicate. In addition, the individual components of the detergent composition should each have an initial free water content (unbound water at 100°C) of leas than 10 percent by weight, more preferably less than 9 percent by weight, and most preferably less than 8 percent by weight. During manufacture the detergent composition may take-up moisture from the atmosphere. As a result, the moisture content of the detergent composition as it is being packaged may be greater than 1 percent by weight, preferably less than 4 percent by weight and most preferably less than 3 percent by weight.
  • [0004]
    Nonaqueous liquid dishwasher detergent compositions which contain enzymes can be made more stable and to have a high activity, if the initial free water content of the detergent composition less than 6 percent by weight, more preferably less than 4 percent by weight and most preferably less than 3 percent by weight. A key aspect is to keep the free water (non-chemically bonded water) in the detergent composition at a minimum. It is critical that water not be added to the composition. Absorbed and absorbed water are two types of free water and comprise the usual free water found in the detergent composition. Free water will have the affect of deactivating the enzyme. Furthermore, the pH of 1.0 weight % of an aqueous solution of a liquid detergent composition must be less than 11.0 more preferably less than 10.8, and most preferably less than 10.5. This low alkalinity of the dishwashing detergent will also increase the stability of the detergent composition which contains a mixture of enzymes, thereby providing a higher initial activity of the mixture of the enzymes and the maintenance of this initial high activity.
  • [0005]
    The free water content of the dishwashing detergent compositions of the instant invention can be controlled to a Iarge extent by using components that have a low initial water content and a low hygroscopicity. The individual components of the instant composition should have a water content of less than 10 percent by weight, more preferably less than 8 percent by weight, and moat preferably leas than 4 percent by weight. In addition, the organic components of the dishwashing detergent composition should have low hydroxyl group content to decrease the hydrogen bonding absorption of water. In place of the carrier such as ethylene glycols or glycerols, relatively low hydroxyl content-anhydrous organics such as alcohol ethers and polyalkylene glycols can be used. In place of polyacid suspending agents normally used in liquid automatic dishwashing detergent compositions such as polyacrylic acid or salts of polyacrylic acids, there should be used polyacid/acid anhydride copolymers such as polyacrylic acid/acid anhydride copolymers. Maleic anhydride is a suitable acid anhydride. The net result is a decreased hydroxyl group content which translates to a decreased hygroscopicity of the detergent composition which helps maintain the stability and the activity.
  • SUMMARY OF THE INVENTION
  • [0006]
    This invention is directed to producing a nonaqueous liquid enzyme containing automatic dishwashing detergent compositions which have an increased chemical stability and essentially a constant activity at wash operating temperatures of 100°F to 140°F. This is accomplished by controlling the alkalinity and the hygroscopicity of the detergent composition and using a novel mixture of enzymes. An alkali metal silicate is used in the dishwashing detergent compositions which may have a free water content of less than 6 percent by weight, more preferably less than 4 percent by weight, and most preferably less than 3 percent by weight throughout its usage. The Na₂O:SiO₂ ratio can exceed 1:3.22 but should not be lower than 1:2. In order to achieve this low free water content, the water content of each of the detergent components should be less than 1 percent by weight, more preferably less than 0.75 percent by weight, and most preferably less than 0.5 percent by weight. Furthermore, each of the organic components should have a low hydroxyl group content in order to decrease the potential amount of hydrogen bonded water in the composition.
  • [0007]
    Conventional automatic dishwashing compositions usually contain a low foaming surface-active agent, a carrier solvent which is usually water, a chlorine bleach, alkaline builder materials, and usually minor ingredients and additives. The incorporation of chlorine bleach requires special processing and storage precautions to protect composition components which are subject to deterioration upon direct contact with the active chlorine. The stability of the chlorine bleach is also critical and raises additional processing and storage difficulties. In addition, it is known that automatic dishwasher detergent compositions may tarnish silverware and damage metal trim on china as a result of the presence of a chlorine-containing bleach therein. Accordingly, there is a standing desire to formulate detergent compositions for use in automatic dishwashing operations which are free of active chlorine and which are capable of providing overall hard surface cleaning and appearance benefits comparable to or better than active chlorine-containing detergent compositions. This reformulation is particularly delicate in the context of automatic dishwashing operations, since during those operations, the active chlorine prevents the formation and/or deposition of troublesome protein and protein-grease complexes on the hard dish surfaces. No surfactant system currently known is capable of adequately performing this function.
  • [0008]
    Various attempts have been made to formulate bleach-free low foaming detergent compositions for automatic dishwashing machines, containing particular low foaming nonionics, builders, filler materials and enzymes. US Patent 3,472,783 to Smille recognized that degradation can occur when an enzyme is added to a highly alkaline automatic dishwashing detergent.
  • [0009]
    French Patent No. 2,102,851 to Colgate-Palmolive, pertains to rinsing and washing compositions for use in automatic dishwashers. The compositions disclosed have a pH of 6 to 7 and contain an amylolytic and, if desired, a proteolytic enzyme, which have been prepared in a special manner from animal pancreas and which exhibit a desirable activity at a pH in the range of 6 to 7. German Patent No. 2,038,103 to Henkel & Co. relates to aqueous liquid or pasty cleaning compositions containing phosphate salts, enzymes and an enzyme stabilizing compound. US Patent No. 3,799,879 to Francke et al, teaches a detergent composition for cleaning dishes, with a pH of from 7 to 9 containing an amylolytic enzyme, and in addition, optionally a proteolytic enzyme.
  • [0010]
    US Patent 4,101,457 to Place et al teaches the use of a proteolytic enzyme having a maximum activity at a pH of 12 in an automatic dishwashing detergent.
  • [0011]
    US Patent 4,162,987 to Maguire et al teaches a granular or liquid automatic dishwashing detergent which uses a proteolytic enzyme having a maximum activity at a pH of 12 as well as an amylolytic enzyme having a maximum activity at a pH of 8.
  • [0012]
    US Patent No 3,827,938 to Aunstrup et al, discloses specific proteolytic enzymes which exhibit high enzymatic activities in highly alkaline systems. Similar disclosures are found in British Patent Specification No. 1,361,386, to Novo Terapeutisk Laboratorium A/S. British Patent Specification No. 1,296,839, to Novo Terapeutisk Laboratorium A/S, discloses specific amylolytic enzymes which exhibit a high degree of enzymatic activity in alkaline systems.
  • [0013]
    Thus, while the prior art clearly recognizes the disadvantages of using aggressive chlorine bleaches in automatic dishwashing operations and also suggests bleach-free compositions made by leaving out the bleach component, said art disclosures are silent how to formulate an effective bleach-free automatic dishwashing compositions capable of providing superior performance at low alkalinity levels during conventional use.
  • [0014]
    US Patent Nos. 3,840,480; 4,568,476; 3,821,118 and 4,501,681 teach the use of enzymes in automatic dishwashing detergents.
  • [0015]
    The aforementioned prior art fails to provide a liquid automatic dishwashing detergent which contains a mixture of enzymes for the simultaneous degradation of both proteins and starches, wherein the combination of enzymes have a maximum activity at a pH of less than 10.6 and the liquid automatic dishwashing detergent has optimized cleaning performance in a temperature range of 100°F to 140°F.
  • [0016]
    It is an object of this invention to incorporate a unique enzyme mixture of proteolytic and amylolytic enzymes in dishwasher detergent compositions which can be used in automatic dishwashing operations capable of providing at least equal or better performance at operating temperatures of 100°F to 140°F.
  • [0017]
    Both protein soils and carbohydrate soils are extremely difficult to remove form dishware. The use of bleach in automatic dishwashing compositions helps in the removal of protein soils and high alkalinity of these automatic dishwashing compositions helps in the removal of carbohydrate soils, but even with bleach and high alkalinity these protein and carbohydrate soils are not completely removed. The use of a protease enzyme in the automatic dishwashing compositions improves the removal of protein soils such as egg and milk from dishware and the use of an amylase enzyme improves the removal of carbohydrate soils such as starch from dishware.
  • Brief Description of the Drawings
  • [0018]
    Figure 1 illustrates a graph of a percent of egg removal at various water and temperature conditions for a combination of Maxatase and Protein Engineered Maxacal 42 (Maxapem 42) enzymes versus wash temperature of cleaning at a pH of 9.1.
  • [0019]
    Figure 2 illustrates a graph of a percent of egg removal at various water and temperature conditions for Protein Engineered Maxacal 42 (Maxapem 42) enzymes versus wash temperature of cleaning at a pH of 9.1.
  • [0020]
    Figure 3 illustrates a graph of a percent of egg removal at various water and temperature conditions for Maxatase enzyme versus wash temperature of cleaning at a pH of 9.1.
  • [0021]
    Figure 4 illustrates a graph of a percent of egg removal at various water and temperature conditions for Maxacal enzyme versus wash temperature of cleaning at a pH of 9.1.
  • [0022]
    Figure 5 illustrates a graph of a percent of egg removal at various water and temperature conditions for Maxacal enzyme versus wash temperature of cleaning at a pH of 8.8.
  • DETEAILED DESCRIPTION
  • [0023]
    The present invention relates to a nonaqueous liquid automatic dishwashing detergent compositions which comprise a nonionic surfactant, a nonaqueous liquid carrier, sodium silicate, a metal inorganic builder salt and a mixture of an amylase enzyme and one or two protease enzymes, wherein the composition comprises in percent by weight :
    and, optionally, a lipase enzyme, wherein the nonaqueous liquid automatic dishwashing detergent composition has preferably a pH of less than 10.5 and the dishwashing detergent composition exhibits maximum cleaning efficiency for both proteins and starches at a wash temperature of 100°F to 140°F.
  • [0024]
    The liquid nonionic surfactants that can be, optionally, used in the present nonaqueous liquid automatic dishwasher detergent compositions are well known. A wide variety of the these surfactants can be used.
  • [0025]
    The nonionic synthetic organic detergents are generally described as ethoxylated propoxylated fatty alcohols which are low-foaming surfactants and are possibly capped, characterized by the presence of an organic hydrophobic group and an organic hydrophilic group and are typically produced by the condensation of an organic aliphatic or alkyl aromatic hydrophobic compound with ethylene oxide and/or propylene oxide. Practically any hydrophobic compound having a carboxyl, hydroxy and amido or amino group with a free hydrogen attached to the nitrogen can be condensed with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a nonionic detergent. The length of the hydrophilic or polyoxy ethylene/propylene chain can be readily adjusted to achieve the desired balance between the hydrophobic and hydrophilic groups. Typical suitable nonionic surfactants are those disclosed in US Patent Nos. 4,316,812 and 3,630,929.
  • [0026]
    Preferably, the nonionic detergents that are used are the low foaming poly-lower alkoxylated lipophiles, wherein the desired hydrophile-lipophile balance is obtained from addition of a hydrophilic poly-lower alkoxy group to a lipophilic moiety. A preferred class of the nonionic detergent employed is the poly-lower alkoxylated higher alkanol wherein the alkanol is of 9 to 18 carbon atoms and wherein the number of moles of lower alkylene oxide (of 2 or 3 carbon atoms) is from 3 to 15. Of such materials it is preferred to employ those wherein the higher alkanol is a high fatty alcohol of 9 to 11 or 12 to 15 carbon atom and which contain from 5 to 8 or 5 to 9 lower alkoxy groups per mole. Preferably, the lower alkoxy is ethoxy but in some instances, it may be desirably mixed with propoxy, the latter, if present, usually being minor (no more than 50%) portion. Exemplary of such compounds are those wherein the alkanol is of 12 to 15 carbon atom and which contain 7 ethylene oxide groups per mole.
  • [0027]
    Useful nonionics are represented by the low foaming Plurafac series from BASF Chemical Company which are the reaction product of a higher linear alcohol and a mixture of ethylene and propylene oxides, containing a mixed chain of ethylene oxide and propylene oxide, terminated by a hydroxyl group. Examples include Product A (a C₁₃-C₁₅ fatty alcohol condensed with 6 moles ethylene oxide and 3 moles propylene oxide), Product B (a C₁₃-C₁₅ fatty alcohol condensed with 7 mole propylene oxide and 4 mole ethylene oxide), and Product C (a C₁₃-C₁₅ fatty alcohol condensed with 5 moles propylene oxide and 10 moles ethylene oxide). A particularly good surfactant is Plurafac 132 which is a capped nonionic surfactant. Another group of low foam liquid nonionics are available from Shell Chemical Company, Inc. under the Dobanol trademark: Dobanol 91-5 is an ethoxylated C₉-C₁₁ fatty alcohol with an average of 5 moles ethylene oxide and Dobanol 25-7 is an ethoxylated C₁₂-C₁₅ fatty alcohol with an average of 7 moles ethylene oxide.
  • [0028]
    Another liquid nonionic surfactant that can be used is sold under the tradename Lutensol SC 9713.
  • [0029]
    Synperonic nonionic surfactant such as Synperonic LF D25 or LF RA 30 are especially preferred nonionic surfactants that can be used in the nonaqueous liquid automatic dishwasher detergent compositions of the instant invention. Other useful nonionic surfactants are Synperonic RA 30, Synperonic RA 40 and Synperonic RA 340. The Synperonic surfactants are especially preferred because they are biodegradable and low foaming.
  • [0030]
    Poly-Tergent nonionic surfactants from Olin Organic Chemicals such as Poly-Tergent SLF-18, a biodegradable, low-foaming surfactant is specially preferred for the powdered automatic dishwasher detergent compositions of this instant invention. Poly-Tergent SLF-18, a water dispersible, having a low cloud point has lower surface tension and lower foaming is very suitable for automatic dishwasher detergent.
  • [0031]
    Other useful surfactants are Neodol 25-7 and Neodol 23-6.5, which products are made by Shell Chemical Company, Inc. The former is a condensation product of a mixture of higher fatty alcohols averaging 12 to 13 carbon atoms and the number of ethylene oxide groups present averages 6.5. The higher alcohols are primary alkanols. Other examples of such detergents include Tergitol 15-S-7 and Tergitol 15-S-9 (registered trademarks), both of which are linear secondary alcohol ethoxylates made by Union Carbide Corp. The former is mixed ethoxylation product of 11 to 15 carbon atoms linear secondary alkanol with seven moles of ethylene oxide and the latter is a similar product but with nine moles of ethylene oxide being reacted. Another useful surfactant is Tergitol MDS-42 a mixed ethoxylation product of 13-15 cations alcohols with 10 moles of EO and 5 moles of PO.
  • [0032]
    Also useful in the present compositions as a component of the nonionic detergent are higher molecular weight nonionics, such as Neodol 45-11, which are similar ethylene oxide condensation products of higher fatty alcohols, with the higher fatty alcohol being of 14 to 15 carbon atoms and the number of ethylene oxide groups per mole being 11. Such products are also made by Shell Chemical Company.
  • [0033]
    In the preferred poly-lower alkoxylated higher alkanols, to obtain the best balance of hydrophilic and lipophilic moieties the number of lower alkoxies will usually be from 40% to 100% of the number of carbon atoms in the higher alcohol, preferably 40 to 60% thereof and the nonionic detergent will preferably contain at least 50% of such preferred poly-lower alkoxy higher alkanol.
  • [0034]
    The alkyl polysaccharides surfactants, which are used alone in conjunction with the aforementioned surfactant and have a hydrophobic group containing from 8 to 20 carbon atoms, preferably from 10 to 16 carbon atoms, most preferably from 12 to 14 carbon atoms, and polysaccharide hydrophilic group containing from 1.5 to 10, preferably from 1.5 to 4, most preferably from 1.6 to 2.7 saccharide units (e.g., galactoside, glucoside, fructoside, glucosyl, fructosyl; and/or galactosyl units). Mixtures of saccharide moieties may be used in the alkyl polysaccharide surfactants. The number x indicates the number of saccharide units in a particular alkyl polysaccharide surfactant. For a particular alkyl polysaccharide molecule x can only assume integral values. In any physical sample of alkyl polysaccharide surfactants there will be in general molecules having different x values. The physical sample can be characterized by the average value of x and this average value can assume non-integral values. In this specification the values of x are to be understood to be average values. The hydrophobic group (R) can be attached at the 2-, 3-, or 4- positions rather than at the l-position, (thus giving e.g. a glucosyl or galactosyl as opposed to a glucoside or galactoside). However, attachment through the 1-position, i.e., glucosides, galactoside, fructosides, etc., is preferred. In the preferred product the additional saccharide units are predominately attached to the previous saccharide unit's 2-position. Attachment through the 3-, 4-, and 6-positions can also occur. Optionally and less desirably there can be a polyalkoxide chain joining the hydrophobic moiety (R) and the polysaccharide chain. The preferred alkoxide moiety is ethoxide.
  • [0035]
    Typical hydrophobic groups include alkyl groups, either saturated or unsaturated, branched or unbranched containing from 8 to 20, preferably from 10 to 18 carbon atoms. Preferably, the alkyl group is a straight chain saturated alkyl group. The alkyl group can contain up to 3 hydroxy groups and/or the polyalkoxide chain can contain up to 30, preferably less than 10 alkoxide moieties.
  • [0036]
    Suitable alkylpolysaccharides are decyl, dodecyl, tetradecyl, pentadecyl, hexadecyl, and octadecyl, di-, tri-, tetra-, penta- and hexaglucosides, galactosides, lactosides, fructosides, fructosyls, lactosyls, glucosyls and/or galactosyls and mixtures thereof.
  • [0037]
    The alkyl monosaccharides are relatively less soluble in water than the higher alkyl polysaccharides. When used in admixture with alkyl polysaccharides, the alkyl monosaccharides are solubilized to some extent. The use of alkyl monosaccharides in admixture with alkyl polysaccharides is a preferred mode of carrying out the invention. Suitable mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexaglucosides.
  • [0038]
    The preferred alkyl polysaccharides are alkyl polyglucosides having the formula

            R₂O(CnH2nO)r(Z)x


    wherein Z is derived from glucose, R is a hydrophobic group selected from the group consisting of alkyl, alkylphenyl, hydroxyalkylphenyl, and mixtures thereof in which said alkyl groups contain from 10 to 18, preferably from 12 to 14 carbon atoms; n is 2 or 3 preferably 2, r is from 0 to 10, preferably 0; and x is from 1.5 to 8, preferably from 1.5 to 4, most preferably from 1.6 to 2.7. To prepare these compounds a long chain alcohol (R₂OH) can be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (R₁OH) an be reacted with glucose, in the presence of an acid catalyst to form the desired glucoside. Alternatively the alkyl polyglucosides can be prepared by a two step procedure in which a short chain alcohol (C₁₋₆) is reacted with glucose or a polyglucoside (x=2 to 4) to yield a short chain alkyl glucoside (x=1 to 4) which can in turn be reacted with a longer chain alcohol (R₂OH) to displace the short chain alcohol and obtain the desired alkyl polyglucoside. If this two step procedure is used, the short chain alkyl glucoside content of the final alkyl polyglucoside material should be less than 50%, preferably less than 10%, more preferably less than 5%, most preferably 0% of the alkyl polyglucoside.
  • [0039]
    The amount of unreacted alcohol (the free fatty alcohol content) in the desired alkyl polysaccharide surfactant is preferably less than 2%, more preferably less than 0.5% by weight of the total of the alkyl polysaccharide. For some uses it is desirable to have the alkyl monosaccharide content less than 10%.
  • [0040]
    The used herein, "alkyl polysaccharide surfactant" is intended to represent both the preferred glucose and galactose derived surfactants and the less preferred alkyl polysaccharide surfactants. Throughout this specification, "alkyl polyglucoside" is used to include alkyl polyglycosides because the stereochemistry of the saccharide moiety is changed during the preparation reaction.
  • [0041]
    An especially preferred APG glycoside surfactant is APG 625 glycoside manufactured by the Henkel Corporation of Ambler, PA. APG 25 is a nonionic alkyl polyglycoside characterized by the formula:

            CnH2n+1O(C₆H₁₀O₅)xH


    wherein n=10 (2%); n=12 (65%); n=14 (21-28%); n=16 (4-8%) and n=18 (0.5%) and x (degree of polymerization) = 1.6. APG 625 has: a pH of 6-8 (10% of APG 625 in distilled water); a specific gravity at 25°C of 1.1 g/ml; a density at 25°C of 9.1 lbs/gallon; a calculated HLB of 12.1 and a Brookfield viscosity at 35°C, 21 spindle, 5-10 RPM of 3,000 to 7,000 cps.
  • [0042]
    Mixtures of two or more of the liquid nonionic surfactants can be used and in some cases advantages can be obtained by the use of such mixtures.
  • [0043]
    The nonaqueous liquid nonionic surfactant has dispersed therein fine particles or organic and/or inorganic detergent builders. A preferred solid builder salt is an alkali metal polyphosphate such as sodium tripolyphosphate ("TPP"). In place of all or part of the alkali metal polyphosphate one or more other detergent builder salts can be used. Suitable other builder salts are alkali metal carbonates, borates, phosphates, bicarbonates, silicates, lower polycarboxylic acid salts, and polyacrylates, polymaleic anhydrides and copolymers of polyacrylates and polymaleic anhydrides and polyacetal carboxylates.
  • [0044]
    Specific examples of such builders are sodium carbonate, potassium carbonate, sodium tetraborate, sodium pyrophosphate, sodium tripolyphosphate, potassium tripolyphosphate, potassium pyrophosphate, sodium bicarbonate, sodium hexametaphosphate, sodium sesquicarbonate, sodium mono and diorthophosphate, and potassium bicarbonate. The builder salts can be used alone with the nonionic surfactant or in an admixture with other builders. Typical builders also include those disclosed in U.S. Pat Nos. 4,316,812, 4,264,466 and 3,630,929 and those disclosed in U.S. Patent Nos. 4,144,226, 4,135,092 and 4,146,495.
  • [0045]
    A preferred builder salt is sodium tripolyphosphate (TPP). The TPP is a blend of anhydrous TPP and a small amount of TPP hexahydrate such that the chemically bound water which corresponds to one H₂O per pentasodium tripolyphosphate molecule. Such TPP may be produced by treating anhydrous TPP with a limited amount of water. The presence of the hexahydrate slows down the rapid rate of solution of the TPP in the wash bath and inhibits caking. One suitable TPP is sold under the name Thermphos NW. The particles size of the Thermphos NW TPP, as supplied, is usually averages 200 microns with the largest particles being 400 microns.
  • [0046]
    The alkali metal silicates are useful builder salts which also function to make the composition anti-corrosive so that damage to eating utensils and to automatic dishwashing machine parts is minimized. Sodium silicates of Na₂O/SiO₂ ratios of from 1:1 to 1:2.4 especially 1:2 to 1:3 are preferred. Potassium silicates of the same ratios can also be used. The preferred alkali metal silicates are sodium disilicate and sodium metasilicate.
  • [0047]
    Another class of builders useful herein are the water insoluble aluminosilicates, both of the crystalline and amorphous type. Various crystalline zeolites (i.e. alumino-silicates) are described in British Patent No. 1,504,168, U.S. Patent No. 4,409,136 and Canadian Patent Nos. 1,072,835 and 1,087,477. An example of amorphous zeolites useful herein can be found in Belgium Patent No. 835,351. The zeolites generally have the formula

            (M₂O)x(Al₂O₃)y(SiO₂)x wH₂O


    wherein x is 1, y is from 0.8 to 1.2 and preferably 1, z is from 1.5 to 3.5 or higher and preferably 2 to 3 and w is from 0 to 9, preferably 2.5 to 6 and M is preferably sodium. A typical zeolite is type A or similar structure, with type 4A particularly preferred. The preferred aluminosilicates have calcium ion exchange capacities of 200 milliequivalents per gram or greater, e.g. 400 meq/g.
  • [0048]
    In conjunction with the builder salt are optionally used a low molecular weight polyacrylates which have a molecular weight of 1,000 to 100,000 more preferably 2,000 to 80,000. A preferred low molecular weight polyacrylate is Sokalantm CP45 manufactured by BASF and having a molecular weight of 4,500. Another preferred low molecular weight polyacrylate is Acrysoltm 45ND manufactured by Rohm and Haas and having a molecular weight of 45,000. A suitable suspending and anti-redepositing agent consists of a copolymer of a polyacid and an acid anhydride. Such a material should have a water absorption at 38°C and 78 percent relative humidity of less than 40 percent and preferably less than 30 percent. The builder is commercially available under the tradename of Sokalan CP 45. This is a partially neutralized copolymer of acrylic acid and maleic acid sodium salt. This suspending and anti-deposition agent also serves to inhibit encrustation, i.e. inhibits the formulation and precipitation of dicalcium phosphate. This suspending agent has a low hygroscopicity as a result of a decreased hydroxyl group content. An objective is to use suspending and anti-redeposition agents that have a low hygroscopicity. Copolymerized polyacids have this property, and particularly when partially neutralized. Acusol™ 640 ND provided by Rohm & Haas is another useful suspending agent. Other builder salts which can be mixed with the sodium carbonate are gluconates and nitriloacetic acid salts.
  • [0049]
    The stability against settling properties can be improved by the addition to the composition of a small effective amount of phosphoric ester and the viscosity and anti-gel properties of the composition can be improved by adding to the composition an effective amount of an alkylene glycol monoalkyl ether.
  • [0050]
    In accordance with an embodiment of the present invention the stability of the suspension is increased by including in the composition an acidic organic phosphorus compound having an acidic-POH group. The use of organic phosphoric acid esters as stabilizing additives to nonionic laundry detergent compositions containing polyphosphate builders is well known.
  • [0051]
    The acidic organic phosphorus compound may be, for instance, a partial ester of phosphoric acid and an alcohol such as an alkanol which has a lipophilic character, having, for instance, more than 5 carbon atoms, e.g. 8 to 20 carbon atoms. A specific example is a partial ester of phosphoric acid and a C₁₆ to C₁₈ alkanol (Empiphos 5632 from Marchon); it is made up of 35% monoester and 65% diester. The inclusion of quite small amounts of the acidic organic phosphorus compound makes the suspension significantly more stable against settling on standing but remains pourable and decreases its plastic viscosity. It is believed that the use of the acidic phosphorus compound may result in the formation of a high energy physical bond between the -POH portion of the molecule and the surfaces of the inorganic polyphosphate builder so that these surfaces take on an organic character and become more compatible with the nonionic surfactant.
  • [0052]
    The thickening agents that can be used are those that will swell and develop thixotropic properties in a nonaqueous environment. These include organic polymeric materials and inorganic and organic modified clays. Essentially, any clay can be used as long as it will swell in a nonaqueous medium and develop thixotropic properties. A preferred clay is bentonite organoclay. A swelling agent is used with the bentonite clay. The preferred swelling agent is a combination of propylene carbonate and tripropylene glycol methyl ether. However, any other substance that will cause bentonite to swell in a nonaqueous environment and thus develop thixotropic properties can be used.
  • [0053]
    Suitable polymeric thickening agents are polycarboxylate polymers such as Carbopol polymers manufactured by B.F. Goodrich. Carbopol 614 and Carbopol 617 are especially preferred polymeric thickening agents. Another class of suitable thickening agents are silicas such as Cab-O-Sil which are useful at a concentration of 0.1 to 3.0 weight percent. Another class of thickening agents are polyacrylates having a molecular weight of 1,000 to 50,000. An especially preferred polyacrylate is Sokalan CP 45, manufactured by BASF and Acrysoltm 45ND manufactured by Rohm Haas. These polyacrylates are used at a concentration level of 0.1 to 10 weight percent.
  • [0054]
    Other polymeric thickening agents are low molecular weight associative thickeners such as Dapral(R) T210 and T212 from AKZO chemicals. Dapral T210 and T212 are low molecular weight dialkyl polyglycol ethers with an average molecular weight of 8000. They are liquids and soluble and compatible in non-aqueous media. Specially preferred is Dapral T210 in 1-5% and in combination with other thickening agents such as colloidal silica.
  • [0055]
    Essentially, any compatible anti-foaming agent can be used. Preferred anti-foaming agents are silicone anti-foaming agents. These are alkylated polysiloxanes and include polydimethyl siloxanes, polydiethyl siloxanes, polydibutyl siloxanes, phenyl methyl siloxanes, dimethyl silanated silica, trimethysilanated silica and triethylsilanated silica. Suitable anti-foam agents are Silicone L7604 and DB-100. Other suitable anti-foaming agents are Selecore DB 700 used at 0.2 to 1.0 weight %, sodium stearate used at a concentration and of 0.5 to 1.0 weight %. Another class of suitable foam depressants used at concentration levels of 0 to 1.5 weight %, more preferably 0.2 to 1.0 weight %. are the alkyl phosphoric acid esters of the formula
    available from BASF-Wyandotte and the alkyl phosphate esters of the formula
    available from Hooker (SAP) and Knapsack (LPKn-158) in which one or both R groups in each type of ester may be represented independently by a C₁₂₋₂₀ alkyl or ethoxylated alkyl group.
  • [0056]
    The perfumes that can be used include lemon perfume and other natural scents. Essentially, any opacifier pigment that is compatible with the remaining components of the detergent formulation can be used. A useful and preferred opacifier is titanium dioxide.
  • [0057]
    The nonaqueous carrier materials that can be used for the liquid automatic dishwashing detergent compositions are contained in the composition at a concentration level of at least 40 wt.% to 65 wt.%, more preferably at least 45 wt.% to 60 wt.%, are those that have a low hydroscopicity. These include the higher glycols, polyglycols, polyoxides and glycol ethers. Suitable substances are propylene glycol, polyethylene glycol, polypropylene glycol, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether, diethylene glycol monobutyl ether, tripropylene glycol methyl ether, propylene glycol methyl ether (DM), dipropylene glycol methyl ether DPMI, propylene glycol methyl acetate (PMA), dipropylene glycol methyl ether acetate (DPMA), ethylene glycol n-butyl ether and ethylene glycol dipropyl ether. A preferred nonaqueous carrier of the instant invention is polyethylene glycol 200 or polyethylene glycol 300.
  • [0058]
    Other useful solvents are ethylene oxide/propylene oxide, propylene oxide liquid random copolymer such as Synalox so solvent series from Dow Chemical (Synalox 50-50B). Other suitable solvents are propylene glycol ethers such as PnB, DPnB and TPnB (propylene glycol mono n-butyl ether, dipropylene glycol and tripropylene glycol mono n-butyl ether, dipropylene glycol and tripropylene glycol mono n-butyl ethers sold by Dow Chemical under the tradename Dowanol. Also tripropylene glycol mono methyl ether "TPM Dowanol" from Dow Chemical is suitable. Another useful series of solvents are supplied by CCA biochem b.u. of Holland such as Plurasolv RML, Plurasolv REL(s), Plurasolv REL, Plurasolv RIPL and Plurasolv RRBL.
  • [0059]
    Mixtures of PEG solvent with Synalox or PnB, DPnB, TPnB and TPM solvents are also useful. Preferred mixtures are PEG 300/Synalox 50-50B and PEG 300/TPnB in weight ratios of 95:5 to 50:50. EP/PO capped nonionic surfactants can be used as a liquid solvent carrier and an example of such a nonionic surfactant is Plurafac LF 132 sold by BASF.
  • [0060]
    The stabilizing system of the instant compositions comprise a finely divided silica such as Cab-O-Sil M5, PTG or Aerosil 200 which are used at a concentration level of 0 to 4.0 weight percent, more preferably 0.5 to 3.0 weight %. Also employed as a stabilizing system are mixtures of finely divided silica such as Cab-O-Sil, and nonionic associative thickeners such as Dapral T210, T212 (Akzo) which are low molecular weight dialkyl polyglycol ethers with a dumbbell-like structure or Pluracol TH 916 and TH 922 (BASF) associative thickeners having star-like structure with a hydrophilic core and hydrophobic tail. These thickeners are used at concentration levels of 0 to 5.0 weight percent together with 0 to 2.0 weight percent of finely divided silica. Other useful stabilizing systems are blends of organoclay and hydroxypropyl cellulose polymer (HPC). A suitable organoclay is Bentone NL27 gel sold by NL Chemical. A suitable cellulose polymer is Klucel M Cellulose having a molecular weight of 1,000,000 and is sold by Aqualon Company. Bentone gel contains 9% Bentone NL 27 powder (100 percent active), 88 percent TPM solvent (tripropylene glycol mono methyl ether) and 3 percent propylene carbonate (polar additive). The organic modified clay thickeners are used at concentration levels of 0 weight percent to 15 weight percent in conjunction with Klucel M at concentration levels of 0 to 0.5 weight percent, more preferably 0.2 weight percent to 0.4 weight percent. Another useful thickening agent is a high molecular weight long chain fatty alcohol (C₂₀-C₄₀) such as Unilin™ 425 sold by Petrolite chemicals.
  • [0061]
    A key aspect is to keep the free water (non-chemically bounded water) in the detergent composition at a minimum. Absorbed and adsorbed water are two types of free water, and comprise the usual free water found in a detergent composition. Free water will have the affect of deactivating the enzymes.
  • [0062]
    The detergent composition of the present invention can possibly include a peroxygen bleaching agent at a concentration level of 2 to 15 wt.%. The oxygen bleaching agents that can be used are alkali metal perborate, perphthalic acid, percarbonate and perphosphates, and potassium monopersulfate. A preferred compound is sodium perborate monohydrate. The peroxygen bleaching compound is preferably used in admixture with an activator thereof. Suitable activators are those disclosed in U.S. Patent No. 4,264,466 or in column 1 of U.S. Patent No. 4,430,244. Polyacylated compounds are preferred activators. Suitable preferred activators are tetraacetyl ethylene diamine ("TAED"), pentaacetyl glucose, and ethyledine benzoate acetate.
  • [0063]
    The activator which is present at a concentration level of 0.5 to 5.0 wt.% usually interacts with the peroxygen compound to form a peroxyacid bleaching agent in the wash water. It is preferred to include a sequestering agent of high complexing power to inhibit any undesired reaction between such peroxyacid and hydrogen peroxide in the wash solution in the presence of metal ions. Suitable sequestering agents include the sodium salts of nitrilotriacetic acid (NTA), ethylene diamine tetraacetic acid (EDTA), diethylene triamine pentaacetic acid (DETPA), diethylene triamine pentamethylene phosphoric acid (DTPMP) sold under the tradename DEQUEST 2066 and ethylene diamine tetramethylene phosphoric acid (EDITEMPA). The sequestering agents can be used alone or in an admixture.
  • [0064]
    The detergent formulation also contains a ternany mixture of two protease enzymes and an amylase enzyme and, optionally, a lipase enzyme that serve to attack and remove organic residues on glasses, plates, pots, pans and eating utensils. Lipolytic enzymes can also be used in the liquid automatic dishwasher detergent composition. Proteolytic enzymes remove protein residues, lipolytic enzymes fat residues and amylolytic enzymes remove starches. Proteolytic enzymes include the protease enzymes subtilisn, bromelin, papain, trypsin and pepsin. Amylolytic enzymes include alpha-amylase enzymes. Lipolytic enzymes include the lipase enzymes. The preferred amylase enzyme is available under the name Maxamyl, derived from Bacillus liceniformis and is available from Gist-Brocades of the Netherlands in the form of nonaqueous slurry (18 wt.% of enzyme) having an activity of abut 40,000 TA u/g. The preferred protease enzymes are available under the name Maxatase, and is derived from a novel Bacillus strain designated "PB92" wherein a culture of the Bacillus is deposited with the Laboratory for Microbiology of the Technical University of Delft and has the number OR-60 and Maxapem 15 or 42 are derived from Bacillus alcalophylus which is high alkaline mutant proteolytic enzyme and both are available from Gist-brocades, of the Netherlands.
  • [0065]
    Maxtase protease enzyme is a low alkaline B. licheniformis protease 600,000 DU/g which is supplied in a nonaqueous slurry (18 weight percent) by International BioSynthetics (Gist-Brocades). Maxapem 15 or 42 protease enzyme is also supplied in a nonaqueous slurry (18 weight percent) and is available from Gist-Brocades, Maxapem 42 with activity 900,000 ADU/g and Maxapem 15 with activity 400,000 ADU/g. Maxamyl amylase enzyme is a thermostable B. licheniformis alpha-amylase (39,500 TAU/g) which is supplied in a nonaqueous slurry (18 weight percent) by International BioSynthetics (Gist-Brocades). Preferred enzyme activities per wash are Maxapem 42/Maxatase protease 250-1,000 KADU/KDU and Maxamyl 4,000-10,000 TAU per wash. At a concentration level of 1.75%, Maxatase, 1.75% Protein Engineered Maxacal 42 (Maxapem 42) and 1.0% Maxamyl in the instant automatic dishwashing compositions, a 25 gram dose of automatic dishwashing composition per wash delivered 9,875 TAU of Maxamyl amylase and 656,250 DU/ADU of protease enzymes.
  • [0066]
    At a concentration level of 8% of Maxatase and 1.0% of Maxamyl in the instant automatic dishwashing compositions, a 25 gram dose of automatic dishwashing composition per wash delivers 9,875 TAU of Maxamyl amylase and 780,000 DU of Maxatase protease.
  • [0067]
    The weight ratio of the one or two Protease enzymes to the amylolytic enzyme in the nonaqueous liquid automatic dishwasher detergent compositions is 9:1 to 1.1:1 more preferably 8 : 1 to 1.2:1. The weight ratio of Maxatase to Protein Engineered Maxacal enzyme 42 is 1.8:1 to 1:1.
  • [0068]
    The detergent composition can have a fairly wide ranging composition. The surfactant can comprise 0 to 15 percent by weight of the composition, more preferably 2 to 15 percent by weight, and most preferably 4 to 12 percent by weight. The soil suspending agent which is preferably a copolymerized polyacrylic acid will be present in an amount of 0 to 20 percent by weight, more preferably 1 to 10 percent by weight and most preferably 3 to 8 percent by weight. The anti-foaming agent will be present in an amount of 0 to 2.5 percent by weight, more preferably 0.1 to 2.0 percent by weight and moat preferably 0.2 to 1.5 percent by weight. The builder, which is preferably sodium tripolyphosphate, is present in an amount of 10 to 40 percent by weight, more preferably 20 to 38 percent by weight and most preferably 20 to 35 percent by weight.
  • [0069]
    The thickener, which is preferably a bentonite clay gel, is a mixture of propylene carbonate and tri-propylene glycol methyl ether (TPM) and Bentone NL 27 is preferred, it is present in an amount of 0 to 15 percent by weight, more preferably 5 to 10 percent by weight.
  • [0070]
    Other useful thickeners are fatty acid and metal fatty acid salts as described in U.S. Patents 4,752,409 and 4,836,946 are also useful thickeners used at a concentrate level of 0.02 to 5 weight percent, more preferably 0.02 to 3 weight percent, and most preferably 0.05 to 3.0 weight percent. Other useful thickeners are polycarboxylate polymers such as Carbopol polymers manufactured by B.F. Goodrich at concentration levels of 0.1 to 5.0 weight percent and more preferably 0.1 to 3.0 weight percent. Low molecular weight polyacrylate polymers such as Sokolantm CP45, Acusoltm 460ND, and Acrysoltm 45ND are useful as thickeners at concentration levels of 0.1 to 10.0 weight percent, and more preferably at 0.1 to 5.0 weight percent.
  • [0071]
    The alkali silicate, of which sodium silicate is preferred, will be present in an amount of 0 to 15 percent by weight, more preferably 6 to 12 percent by weight and most preferably 3 to 9 percent by weight. The opacifier pigment will be present in an amount of 0.0 to 1.0 percent by weight, more preferably 0.1 to 1.0 percent by weight and most preferably 0.5 percent by weight.
  • [0072]
    The enzymes will be present in slurry form (18% enzyme in polyethylene glycol 400) in an amount of 0.8 to 16.0 percent by weight, more preferably 0.9 to 14.0 percent by weight, and most preferably 1.0 to 12.0 percent by weight. The Maxatase and Protein Engineered Maxacal 42 proteases in the automatic dishwashing composition enzyme will comprise 0.5 to 12.0 percent by weight, more preferably 0.7 to 10.0 weight percent and most preferably 0.8 to 9.0 percent by weight. The amylase enzyme will comprise 0.3 to 6.0 percent by weight, more preferably 0.4 to 3.0 weight percent and most preferably 0.5 to 2.0 weight percent. The lipase enzyme will comprise 0.00 to 8.0 percent by weight of the detergent composition. Other components such as color and perfumes will be comprised of 0.1 to 1.0 percent by weight of the detergent composition. Another suitable lipase is Lipolas 30T from Novo Corporation. Another useful lipase enzyme is Amano PS lipase provided by Amunco International Enzyme Co, Inc. The lipase enzymes are especially beneficial in reducing grease residues and related filming problems on glasses and dishware. The remainder of the detergent composition will be comprised of the nonaqueous carrier. This will range from 15 to 65 weight percent, more preferably 25 to 57 weight percent, and most preferably 40 to 55 weight percent.
  • [0073]
    The detergent formulation is produced by combining the liquid components consisting of the carrier, surfactant and anti-foam agent and then adding the builder salt (TPP), the anti-redeposition agent (copolymerized polyacrylic acid) and alkali metal silicate. This mixture is then ground in a ball mill (Attritor or Netzsch) to a particle size of less than 40 microns, and preferably to a size of 4 to 5 microns. The enzyme mixture is then added. The enzymes preferably will be in a polyethylene glycol slurry. This enzyme mixture is mixed into the ground slurry. Then the thickener, thickener swelling agents, opacifiers, brighteners, stabilizing agents and perfumes are added. After a thorough mixing, the detergent composition is packaged.
  • [0074]
    The concentrated nonaqueous liquid nonionic automatic dishwashing detergent compositions of the present invention disperses readily in the water in the dishwashing machine. The presently used home dishwashing machines have a measured capacity for 80cc or 90 grams of detergent. In normal use, for example, for a full load of dirty dishes 60 grams of powdered detergent are normally used.
  • [0075]
    In accordance with the present invention only 20cc to 35 cc or 40 grams or less of the concentrated liquid nonionic detergent composition is needed, and more preferably 20cc or 25 grams of concentrated liquid is used per dispenser cup. The normal operation of an automatic dishwashing machine can involve the following steps or cycles: washing, rinse cycles with hot water. The entire wash and rinse cycles require 120 minutes. The temperature of the wash water is 100°F to 140°F and the temperature of the rinse water is 100°F to 140°F. The wash and rinse cycles use 8 to 12 liters of water for the wash cycle and 8 to 12 liters of water of the rinse cycle.
  • [0076]
    The highly concentrated nonaqueous liquid automatic dishwashing detergent compositions exhibit excellent cleaning properties of proteinaceous soils such as egg and starchy carbohydrates such as catmeal and minimizes the formation of spots and films on the dishware and glasses. In an embodiment of the invention the stability of the builder salts in the composition during storage and the dispersibility of the composition in water is improved by grinding and reducing the particle size of the solid builders to less than 100 microns, preferably less than 40 microns and more preferably to less than 10 microns. The solid builders are generally supplied in particle sizes of 100, 200 or 400 microns. The nonionic liquid surfactant phase can be possibly mixed with the solid builders prior to carrying out the grinding operation.
  • [0077]
    In the grinding operation it is preferred that the proportion of solid ingredients be high enough (e.g. at least 40%, such as 50%) that the solid particles are in contact with each other and are not substantially shielded from one another by the nonionic surfactant liquid. After the grinding step any remaining liquid nonionic surfactant can be added to the ground formulation. Mills which employ grinding balls (ball mills) or similar mobile grinding elements give very good results. For larger scale work a continuously operating mill in which there are 1 mm. or 1.5 mm diameter grinding balls working in a very small gap between a stator and a rotor operating at a relatively high speed e.g. a CoBall mill or a Netzsch ball mill may be employed; when using such a mill, it is desirable to pass the blend of nonionic surfactant and solids first through a mill which does not effect such fine grinding (e.g. to 40 microns) prior to the step of grinding to an average particle diameter below 10 microns in the continuous ball mill.
  • [0078]
    It is also contemplated within the scope of this invention to form compositions without grinding, wherein he particle size has a distribution of 60-120 microns. In a preferred embodiment the detergent builder particles have a particle size distribution such that no more than 10% by weight of said particles have a particle size of more than 10 microns.
  • DESCRIPTION OF THE PREFERRED EMBODIMENTS Example 1
  • [0079]
    The concentrated nonaqueous liquid dishwasher detergent compositions are formulated from the following ingredients in the amounts specified.
  • Laboratory Cleaning Performance
  • [0080]
    Laboratory performance of the compositions of Example were carried out using multi-soils at various temperatures and water hardness conditions. This is done to show differences between the prototype formulations. Egg soil was prepared by mixing egg yolk with an equal amount of 2.5 N calcium chloride solution. 0.4 grams of this mixture was applied as thin cross-wise film to the usable surface of 7.5 inch china plates. The plates were aged in 50% relative humidity overnight. Oatmeal soil was prepared by boiling 24 grams of Quaker Oats in 400 ml of tap water for ten minutes. 3 grams of this mixture was spread as thin film onto a 7.5 inch china plate. The plates were aged for 2 hours at 80°C (176°F). They were then stored overnight at room temperature. Two plates of each egg and oatmeal were used per wash. The plates were placed in the same positions in the dishwasher. 25 grams of the detergent was used as a single dose per wash. All plates were scored by measuring the percent area cleaned. The multi-soil cleaning test results are reported below. The results tabulated were average of at least 2 runs. Average results reflect the average performance results obtained in three different water conditions in given temperatures and the overall average showed the average results obtained in five temperature in three different water conditions and these results were also shown graphically in Figures 1-4. The performance rating shows a normalized result with Maxacal Protease Enzyme and oatmeal cleaning was not considered in calculations. Maxacal (Composition d) is the worst performer and is not suitable for such high 135-140°F temperature wash conditions. The optimum water temperature recommended by Autodish manufacturers for US is 140°F. Composition a which uses a binary mixture of Maxatase and Maxapem 42 in combination with Maxamyl exhibits the highest performance in a temperature range of 100° to 140°F whereas the Maxatase (Composition c) or Maxapem 42 (Composition b) did not provide as good performance as Composition a.
  • Example 2
  • [0081]
    The concentrated nonaqueous liquid dishwasher detergent compositions were formulated from the following ingredients in the amounts specified.
  • Laboratory Cleaning Performance
  • [0082]
    Laboratory performance of the compositions of Example were carried out using multi-soils at various temperatures and water hardness conditions. This is done to show differences between the prototype formulations. Egg soil was prepared by mixing egg yolk with an equal amount of 2.5 N calcium chloride solution. 0.4 grams of this mixture was applied as thin cross-wise film to the usable surface of 7.5 inch china plates. The plates were aged in 506 relative humidity overnight. Oatmeal soil was prepared by boiling 24 grams of Quaker Oats in 400 ml of tap water for ten minutes. 3 grams of this mixture was spread as thin film onto a 7.5 inch china plate. The plates were aged for 2 hours at 80°C (176°F). They were then stored overnight at room temperature. Two plates of each egg and oatmeal were used per wash. The plates were placed in the same positions in the dishwasher. 25 grams of the detergent was used as a single dose per wash. All plates were scored by measuring the percent area cleaned. The multi-soil cleaning teat results are reported below. The results tabulated were average of at least 2 runs. Average results reflect the average performance results obtained in three different water conditions in given temperatures and the overall average showed the average results obtained in five temperature in three different water conditions and these results were also shown graphically in Figures 3, 4 and 5. The performance rating shows a normalized results with Maxacal Protease Enzyme and oatmeal cleaning was not considered in calculations. Maxacal (Composition C) is the worst performer and is not suitable for such high 135-140°F temperature wash conditions. The optimum water temperature recommended by Autodish manufacturers for US is 140°F. By reducing alkalinity of the formulation, the performance of Maxatase was further improved (composition b). Maxatase (compositions a and b) outperformed Maxacal protease.

Claims (14)

  1. A nonaqueous liquid dishwashing composition comprising in percent by weight :
  2. The nonaqueous liquid dishwashing composition according to claim 1 wherein said dishwashing composition has a pH of less than 10.5.
  3. The nonaqueous liquid dishwashing composition according to claim 1 wherein said dishwashing composition futher contains a lipase enzyme.
  4. The nonaqueous liquid dishwashing composition according to claim 1 wherein said dishwashing composition has a free water content of less than 8 percent by weight.
  5. The nonaqueous liquid dishwashing compositon according to Claim 4 wherein said dishwashing composition has a free water content of less than 4 percent by weight.
  6. The nonaqueous liquid dshwashing according to claim 1 which comprises an effective amount of one or more adjuvants selected from the group consisitng of anti-encrustation agents, oxygen bleaching agents, bleaching agent activators, sequestering agents, anti-corosion agents, anti-foam agents, opacifiers and perfumes.
  7. The nonaqueous liquid dishwashing composition according to claim 1 wich includes 0 to 20 percent by weight a copolymerized polyacrylic acid.
  8. The nonaqueous liquid dishwashing composition according to Claim 1 which includes 0 to 8.0 weight percent of a lipase enzyme.
  9. The nonaqueous liquid dishwashing composition according to Claim 1 which contains an alkali metal perborate.
  10. The nonaqueous liquid dishwashing composition according to Claim 9 which contains an alkali metal perborate activator.
  11. The nonaqueous liquid dishwashing composition according to Claim 1, wherein said two protease enzymes are Maxatase, and Maxapem 15 or Maxapem 42 and said amylase enzyme is Maxamyl amylase enzyme, a weight ratio of said protease enzyme to said amylase enzyme being 6:1 to 1.1:1
  12. The nonaqueous liquid dishwashing composition according to Claim 1 wherein said stabilizer is a finely divided silica.
  13. The nonaqueous liquid dishwashing composition according to Claim 1, wherein said protease enzyme is Maxatase protease enzyme and said amylase enzyme is Maxamyl amylase enzyme, a weight ratio of said protease enzyme to said amylase enzyme being 10:1 to 1.1:1.
  14. A process for washing dishware in an a automatic dishwasher comprising washing said dishware at operating temperatures of 100°F to 140°F with a composition as defined in anyone of the preceding claims.
EP19920401478 1991-05-31 1992-05-29 Nonaqueous liquid automatic dishwashing composition containing enzymes Expired - Lifetime EP0518720B1 (en)

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Cited By (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0611206A2 (en) * 1993-02-08 1994-08-17 Colgate-Palmolive Company Nonaqueous gelled automatic diswashing composition containing enzymes
WO1998000511A2 (en) * 1996-06-28 1998-01-08 The Procter & Gamble Company Nonaqueous detergent compositions containing enzymes
EP1036840A2 (en) * 1999-03-17 2000-09-20 Kao Corporation Detergent composition
WO2001036290A1 (en) 1999-11-17 2001-05-25 Reckitt Benckiser (Uk) Limited Injection-moulded water-soluble container
WO2002016207A1 (en) 2000-08-25 2002-02-28 Reckitt Benckiser (Uk) Limited Process and mould for thermoforming containers
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WO2003062085A1 (en) * 2002-01-26 2003-07-31 Aquasol Limited Cutting or perforating water-soluble film
WO2003089329A1 (en) 2002-04-20 2003-10-30 Reckitt Benckiser N.V. Water-soluble containers
WO2005121302A1 (en) 2004-06-11 2005-12-22 Reckitt Benckiser N.V. Process for preparing water-soluble articles
WO2006095190A2 (en) 2005-03-10 2006-09-14 Reckitt Benckiser N.V. Process for the preparation of a package containing compacted composition and the package obtained with this process
US7407923B2 (en) 2002-02-26 2008-08-05 Reckitt Bencklser N.V. Packaged detergent composition
WO2009016370A2 (en) 2007-07-31 2009-02-05 Reckitt Benckiser N.V. Improvements in or relating to compositions
US7507698B2 (en) 2002-02-27 2009-03-24 Reckitt Benckiser N.V. Textile articles for washing and cleaning applications
US7543707B2 (en) 2003-05-20 2009-06-09 Reckitt Benckiser (Uk) Limited Water soluble container
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WO2011049945A2 (en) 2009-10-23 2011-04-28 Danisco Us Inc. Methods for reducing blue saccharide
US8105531B1 (en) 2010-12-21 2012-01-31 Ecolab Usa Inc. Corrosion inhibition of hypochlorite solutions using polyacrylate and Ca
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US8323945B2 (en) 2008-06-06 2012-12-04 Danisco Us Inc. Variant alpha-amylases from Bacillus subtilis and methods of uses, thereof
US8496853B2 (en) 2010-12-21 2013-07-30 Ecolab Usa Inc. Corrosion inhibition of hypochlorite solutions
US8507243B2 (en) 2008-09-25 2013-08-13 Danisco Us Inc. Alpha-amylase blends and methods for using said blends
US8557178B2 (en) 2010-12-21 2013-10-15 Ecolab Usa Inc. Corrosion inhibition of hypochlorite solutions in saturated wipes
US8603392B2 (en) 2010-12-21 2013-12-10 Ecolab Usa Inc. Electrolyzed water system
US9040278B2 (en) 2008-06-06 2015-05-26 Danisco Us Inc. Production of glucose from starch using alpha-amylases from Bacillus subtilis
US9040279B2 (en) 2008-06-06 2015-05-26 Danisco Us Inc. Saccharification enzyme composition and method of saccharification thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2355908A1 (en) * 1976-06-24 1978-01-20 Procter & Gamble A detergent composition containing enzymes for automatic dishwashing
US4511490A (en) * 1983-06-27 1985-04-16 The Clorox Company Cooperative enzymes comprising alkaline or mixtures of alkaline and neutral proteases without stabilizers
EP0171007A2 (en) * 1984-08-04 1986-02-12 Henkel Kommanditgesellschaft auf Aktien Dish cleaning agent
GB2194546A (en) * 1986-08-28 1988-03-09 Colgate Palmolive Co Nonaqueous liquid detergent composition
EP0407225A1 (en) * 1989-07-07 1991-01-09 Unilever Plc Enzymes and enzymatic detergent compositions
EP0425214A2 (en) * 1989-10-23 1991-05-02 Unilever Plc Enzyme-containing detergent compositions and their use

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2355908A1 (en) * 1976-06-24 1978-01-20 Procter & Gamble A detergent composition containing enzymes for automatic dishwashing
US4511490A (en) * 1983-06-27 1985-04-16 The Clorox Company Cooperative enzymes comprising alkaline or mixtures of alkaline and neutral proteases without stabilizers
EP0171007A2 (en) * 1984-08-04 1986-02-12 Henkel Kommanditgesellschaft auf Aktien Dish cleaning agent
GB2194546A (en) * 1986-08-28 1988-03-09 Colgate Palmolive Co Nonaqueous liquid detergent composition
EP0407225A1 (en) * 1989-07-07 1991-01-09 Unilever Plc Enzymes and enzymatic detergent compositions
EP0425214A2 (en) * 1989-10-23 1991-05-02 Unilever Plc Enzyme-containing detergent compositions and their use

Cited By (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0611206A3 (en) * 1993-02-08 1995-06-14 Colgate Palmolive Co Nonaqueous gelled automatic diswashing composition containing enzymes.
EP0611206A2 (en) * 1993-02-08 1994-08-17 Colgate-Palmolive Company Nonaqueous gelled automatic diswashing composition containing enzymes
WO1998000511A2 (en) * 1996-06-28 1998-01-08 The Procter & Gamble Company Nonaqueous detergent compositions containing enzymes
WO1998000511A3 (en) * 1996-06-28 1998-06-25 Boutique Jean Pol Nonaqueous detergent compositions containing enzymes
US6376447B1 (en) 1996-06-28 2002-04-23 Procter & Gamble Company Nonaqueous detergent compositions containing enzymes
EP1036840A3 (en) * 1999-03-17 2003-01-08 Kao Corporation Detergent composition
EP1036840A2 (en) * 1999-03-17 2000-09-20 Kao Corporation Detergent composition
WO2001036290A1 (en) 1999-11-17 2001-05-25 Reckitt Benckiser (Uk) Limited Injection-moulded water-soluble container
EP1647494A2 (en) 1999-11-17 2006-04-19 Reckitt Benckiser (UK) Limited Injection moulded water-soluble container
EP1447343A2 (en) 1999-11-17 2004-08-18 Reckitt Benckiser (UK) Limited Injection moulded water-soluble container
EP2266889A2 (en) 1999-11-17 2010-12-29 Reckitt Benckiser (UK) Limited Injection-moulded water-soluble container
WO2002016207A1 (en) 2000-08-25 2002-02-28 Reckitt Benckiser (Uk) Limited Process and mould for thermoforming containers
WO2002074628A1 (en) 2001-03-16 2002-09-26 Reckitt Benckiser (Uk) Limited Process for producing a water soluble package
WO2002085707A1 (en) 2001-04-20 2002-10-31 Reckitt Benckiser (Uk) Limited Process for preparing a water-soluble thermeformed container
WO2003062085A1 (en) * 2002-01-26 2003-07-31 Aquasol Limited Cutting or perforating water-soluble film
US7407923B2 (en) 2002-02-26 2008-08-05 Reckitt Bencklser N.V. Packaged detergent composition
US7507698B2 (en) 2002-02-27 2009-03-24 Reckitt Benckiser N.V. Textile articles for washing and cleaning applications
WO2003089329A1 (en) 2002-04-20 2003-10-30 Reckitt Benckiser N.V. Water-soluble containers
US7891515B2 (en) 2002-08-07 2011-02-22 Reckitt Benckiser (Uk) Limited Water soluble container with rigid spacer
US7543707B2 (en) 2003-05-20 2009-06-09 Reckitt Benckiser (Uk) Limited Water soluble container
EP2103679A2 (en) 2003-08-01 2009-09-23 Reckitt-Benckiser (UK) Limited Cleaning tablets or water-softening tablets and their manufacture
EP2208605A1 (en) 2003-08-01 2010-07-21 Reckitt-Benckiser (UK) Limited Method of Lubricating a Particulate Material
EP2208777A1 (en) 2003-08-01 2010-07-21 Beckitt Benckiser (UK) Limited Cleaning tablets or water-softening tablets and their manufacture
WO2005121302A1 (en) 2004-06-11 2005-12-22 Reckitt Benckiser N.V. Process for preparing water-soluble articles
EP2752481A1 (en) 2004-06-11 2014-07-09 Reckitt Benckiser N.V. Process for preparing water-soluble articles
WO2006095190A2 (en) 2005-03-10 2006-09-14 Reckitt Benckiser N.V. Process for the preparation of a package containing compacted composition and the package obtained with this process
EP2944578A1 (en) 2005-03-10 2015-11-18 Reckitt Benckiser N.V. Process for the preparation of a package containing compacted composition and the package obtained with this process
EP2208602A1 (en) 2005-11-16 2010-07-21 Beckitt Benckiser (UK) Limited Container from water-soluble polymer and method of ware washing
EP2428572A2 (en) 2007-03-09 2012-03-14 Danisco US, Inc., Genencor Division Alkaliphilic Bacillus species alpha-amylase variants, compositions comprising alpha-amylase variants, and methods of use
WO2009016370A2 (en) 2007-07-31 2009-02-05 Reckitt Benckiser N.V. Improvements in or relating to compositions
US8975056B2 (en) 2008-06-06 2015-03-10 Danisco Us Inc. Variant alpha-amylases from Bacillus subtilis and methods of uses, thereof
US9040278B2 (en) 2008-06-06 2015-05-26 Danisco Us Inc. Production of glucose from starch using alpha-amylases from Bacillus subtilis
US9040279B2 (en) 2008-06-06 2015-05-26 Danisco Us Inc. Saccharification enzyme composition and method of saccharification thereof
US9090887B2 (en) 2008-06-06 2015-07-28 Danisco Us Inc. Variant alpha-amylases from Bacillus subtilis and methods of use, thereof
US8323945B2 (en) 2008-06-06 2012-12-04 Danisco Us Inc. Variant alpha-amylases from Bacillus subtilis and methods of uses, thereof
US8507243B2 (en) 2008-09-25 2013-08-13 Danisco Us Inc. Alpha-amylase blends and methods for using said blends
WO2011049945A2 (en) 2009-10-23 2011-04-28 Danisco Us Inc. Methods for reducing blue saccharide
US8105531B1 (en) 2010-12-21 2012-01-31 Ecolab Usa Inc. Corrosion inhibition of hypochlorite solutions using polyacrylate and Ca
US8496853B2 (en) 2010-12-21 2013-07-30 Ecolab Usa Inc. Corrosion inhibition of hypochlorite solutions
US8557178B2 (en) 2010-12-21 2013-10-15 Ecolab Usa Inc. Corrosion inhibition of hypochlorite solutions in saturated wipes
US8603392B2 (en) 2010-12-21 2013-12-10 Ecolab Usa Inc. Electrolyzed water system

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