GB2140819A - Built single-phase liquid anionic detergent composition containing stabilized enzymes - Google Patents
Built single-phase liquid anionic detergent composition containing stabilized enzymes Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38663—Stabilised liquid enzyme compositions
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Abstract
A stabilized built single-phase enzyme-containing liquid detergent composition is provided comprising: (a) 8 to 20%, by weight, of a surface active anionic detergent compound; (b) 5 to 25% of a water-soluble non-phosphate detergent builder salt; (c) an effective amount of an enzyme or enzyme mixture selected from alkaline protease enzymes and alpha-amylase enzymes; (d) an enzyme stabilizing system containing, based on the weight of the detergent composition, (i) 12 to 25% of propylene glycol and (ii) 1 to 5% of a boron compound which is boric acid, boric oxide or an alkali metal borate, or a mixture thereof; and (e) 25 to 75% by weight of water. z
Description
SPECIFICATION
Built single-phase liquid anionic detergent composition containing stabilized enzymes
The present invention relates to stable, built, enzyme-containing liquid detergent compositions suitable for laundry or pre-soak formulations. More particularly, the invention relates to aqueous enzyme-containing liquid detergent compositions which contain a non-phosphate detergent builder and which are characterised by being physically stable, clear, single-phase homogeneous liquid compositions.
The formulation of stabilized enzyme-containing liquid detergent compositions has been the focus of much attention in the prior art. The desirability of incorporating enzymes into detergent compositions is primarily due to the effectiveness of proteolytic and amylolytic enzymes in decomposing proteinaceous and starchy materials found on soiled fabrics, thereby facilitating the removal of stains, such as, gravy stains, blood stains, chocolate stains and the like during laundering. However, enzymatic materials suitable for laundry compositions, particularly proteolytic enzymes, are relatively expensive. Indeed, they generally are the most expensive ingredient in a typical commercial liquid detergent composition, even when present in relatively minor amounts. Moreover, enzymes are known to be unstable in aqueous compositions.It is for this reason that an excess of enzymes' is generally required in liquid detergent formulations to compensate for the expected loss of enzyme activity during prolonged periods of storage.
Accordingly, the prior art is replete with suggestions for stabilizing enzyme-containing liquid detergent compositions, and in particular unbuilt liquid compositions by the use of various materials which are incorporated into the composition and serve as enzyme stabilizers.
In the case of liquid detergent compositions containing a builder, the problem of enzyme instability is particularly acute. Primarily this is because detergent builders have a destabilizing effect on enzymes, even in compositions containing enzyme stabilizers which are otherwise effective in unbuilt formulations. Moreover, the incorporation of a builder into a liquid detergent composition poses an additional problem, namely, the ability to form a stable single-phase solution, the solubility of sodium tripolyphosphate, for example, being relatively limited in aqueous compositions, and especially in the presence of anionic and non ionic detergents. Thus, for example, in U.K. Patent Application G.B. 2,079,305, published 20th January, 1982, there is disclosed an aqueous built enzyme-containing liquid detergent composition which is stabilized by a mixture of a polyol and boric acid.The compositions described in the examples, however, rather than being stable, clear, single-phase solutions, are instead turbid suspensions which are susceptible to product separation over prolonged periods of storage. Consequently, the problems of enzyme stability and physical product stability remain as problems yet to be overcome in formulating a commercially acceptable built enzyme-containing liquid detergent composition.
The present invention provides a stabilized aqueous, built, clear, single-phase, enzymecontaining liquid detergent composition comprising:
(a) from about 8 to 20%, by weight, of one or more surface active anionic detergent compounds;
(b) from about 5 to 25%, by weight, of a water-soluble non-phosphate detergent builder salt;
(c) an effective amount of an enzyme or enzyme mixture comprising alkaline protease enzymes and alpha-amylase enzymes;
(d) an enzyme stabilizing system containing, based on the weight of the detergent composition (i) from about 1 2 to 25% of propylene glycol and (ii) from about 1 to 5% of a boron compound consisting of boric acid, boric oxide or an alkali metal borate or mixtures thereof; and
(e) from about 25 to 75% by weight of water.
In accordance with the process of the present invention, laundering of stained and/or soiled materials is effected by contacting such materials with an aqueous solution of the above-defined liquid detergent composition. Unlike the built, enzyme-containing detergent compositions known in the art, the compositions of the present invention are characteristically clear, single-phase homogeneous solutions which are physically stable over prolonged periods of storage and over a wide range of temperature. To avoid product separation, the present compositions are preferably substantially free of phosphate builder salt.
Unlike the enzyme-containing built liquid anionic detergent compositions disclosed in the art, the anionic surfactant in the compositions of the present invention is solubilized in the presence of a builder salt. Moreover, the present enzyme-containing compositions are characterised by the presence of an enzyme-stabilizing system which in addition to providing long-term stability to the enzyme over a wide range of temperatures, serves to enhance the solubility of the anionic surfactant and the non-phosphate builder in the aqueous composition allowing a physically stable single-phase solution to be formed for the particular range of compositions indicated.
The enzyme stabilizing system of the present invention is a mixture of propylene glycol and a boron compound selected from among boric acid, boric oxide and alkali metal borate capable of reacting with propylene glycol. The amount of propylene glycol is from about 1 2 to 25%, preferably from about 1 5 to 20%, by weight, and the amount of the boron compound is from about 1 to 5%, preferably from about 1 to 3%, by weight of the composition.
The alkaline proteolytic enzymes suitable for the compositions of the present invention include the various commercial liquid enzyme preparations which have been adapted for use in detergent compositions, enzyme preparations in powdered form being also useful although, as a general rule, less convenient for incorporation into the built liquid detergent compositions. Thus, suitable liquid enzyme preparations include "Alcalase" and " Esperase" sold by Novo Industries,
Copenhagen, Denmark, and "Maxatase" and "AZ-Protease" sold by Gist-Brocades, Delft, The
Netherlands. Esperase is particularly preferred for the present composition because of its optimized activity at the higher pH values corresponding to built detergent compositions.
Among the suitable a-amylase liquid enzyme preparations are those sold by Novo Industries and Gist-Brocades under the tradenames "Termamyl" and "Maxamyl", respectively.
The synthetic anionic detergent employed in the practice of the present invention may be any of wide variety of such compounds which are well known and are described at length in the text
Surface Active Agents, Vol. II, by Schwartz, Perry and Berch, published in 1 958 by Interscience Publishers, the disclosures pertaining to such detergent being hereby incorporated by reference.
The most preferred anionic detergent compounds are the higher (10 to 1 8 or 20 carbon atoms) alkyl benzene sulphonate salts wherein the alkyl group preferably contains 10 to 1 5 carbon atoms, most preferably being a straight chain alkyl radical of 1 2 to 1 3 carbon atoms.
Preferably, such an alkyl benzene sulphonate has a high content of 3- (or higher) phenyl isomers and a correspondingly low content (usually well below 50%) of 2- (or lower) phenyl isomers; in other words, the benzene ring is preferably attached in large part at the 3, 4, 5, 6 or 7 position of the alkyl group and the content of isomers in which the benzene ring is attached at the 1 or 2 position is correspondingly low. Typical alkyl benzene sulphonate surface active agents are described in U.S. Patent 3,320,174. Of course, more highly branched alkyl benzene sulphonates may also be employed but usually are not preferred, due to their lack of biodegradability.
Other anionic detergents which are useful are the olefin sulphonate salts. Generally, these contain long chain alkenyl sulphonates or long chain hydroxyalkane sulphonates (with the OH being on the carbon atom which is not directly attached to the carbon atom bearing the -SO3H group). The olefin sulphonate detergent usually comprises a mixture of such types of compounds in varying amounts, often together with long chain disulphonates or sulphate-sulphonates. Such olefin sulphonates are described in patents, such as U.S. Patent Nos. 2,061 ,6 1 8; 3,409,637; 3,332,880; 3,420,875; 3,428,654; 3,506,580; and British Patent No.
1 , 1 29,1 58. The number of carbon atoms in the olefin sulphonate is usually within the range of 10 to 25, more commonly 10 to 1 8 or 20, e.g. a mixture principally of C,2, C,4 and C16, having an average of about 14 carbon atoms, or a mixture principally of C,4, C16 and C16, having an average of about 1 6 carbon atoms.
Another class of useful anionic detergents is that of the higher paraffin sulphonates. These may be primary paraffin sulphonates made by reacting long chain alpha-olefins and bisulphites, e.g. sodium bisulphite, or paraffin sulphonates having the sulphonate groups distributed along the paraffin chain, such as the products made by reacting a long chain paraffin with sulphur dioxide and oxygen under ultraviolet light, followed by neutralization with sodium hydroxide or other suitable base (as in U.S. Patents 2,503,280; 2,507,088; 3,260,741; 3,372,188; and
German Patent 735,096). The paraffin sulphonates preferably contain from 1 3 to 1 7 carbon atoms and will normally be the monosulphonate but if desired, may be di-, tri- or higher sulphonates.Typically, the di- and polysulphonates will be employed in admixture with a corresponding monosulphonate, for example, as a mixture of mono- and disulphonates containing up to about 30% of the disulphonate. The hydrocarbon substituent thereof is preferably linear but if desired, branched chain paraffin sulphonates can be employed, although they are inferior with respect to biodegradability.
Other suitable anionic detergents are sulphated ethoxylated higher fatty alcohols of the formula RO(C2H4O)rnSO3M, wherein R represents a fatty alkyl group of from 10 to 1 8 or 20 carbon atoms, m is from 2 to 6 or 8 (preferably having a value from about 1/5 to 1/2 the number of carbon atoms in R) and M is a solubilizing salt-forming cation, such as an alkali metal, ammonium, lower alkylamino or lower alkanol-amino, or a higher alkyl benzene sulphonate wherein the higher alkyl group is of 10 to 1 5 carbon atoms.
Ethylene oxide is the preferred lower alkylene oxide of the anionic alkoxylate detergent, and the proportion thereof in the polyethoxylated higher alkanol sulphate is preferably 2 to 5 moles of ethylene oxide groups present per mole of anionic detergent, with three moles being most preferred, especially when the higher alkanol is of 11 or 1 2 to 1 5 carbon atoms. To maintain the desired hydrophilelipophile balance, when the carbon atom content of the alkyl chain is in the lower portion of the 10 to 1 8 carbon atom range, the ethylene oxide content of the detergent may be reduced to about two moles per mole whereas when the higher alkanol is of 1 6 to 1 8 carbon atoms in the higher part of the range, the number of ethylene oxide groups may be increased to 4 or 5 and in some cases to as high as 8 or 9. Similarly, the salt-forming cation may be varied to obtain the best solubility. It may be any suitably solubilizing metal or
radical but will most frequently be alkali metal, e.g. sodium, or ammonium.If lower alkylamine or alkanolamine groups are utilized the alkyl groups and alkanols will usually contain from 1 to 4 carbon atoms and the amines and alkanolamines may be mono-, di- and tri-substituted, as in
monoethanolamine, diisopropanolamine and trimethylamine.
The poly-lower alkoxy higher alkanol sulphates may be employed in combination with other
preferred anionic detergents such as the higher alkyl benzene sulphonates to provide optimum detergency in the present built liquid detergent compositions. A preferred polyethoxylated alcohol sulphate detergent is available from Shell Chemical Company and is marketed as Neodol (Registered Trade Mark) 25-3S.
Examples of the higher alcohol polyethenoxy sulphates which may be employed in the liquid detergent compositions of the invention include: mixed C,2,5 normal or primary alkyl triethenoxy sulphate, sodium salt; myristyl triethenoxy sulphate, potassium salt; n-decyl diethenoxy sul phase, diethanolamine salt; lauryl diethenoxy sulphate, ammonium salt; palmityl tetraethenoxy sulphate, sodium salt; mixed C1415 normal primary alkyl mixed tri- and tetra-ethenoxy sulphate, sodium salt; stearyl pentaethenoxy sulphate, trimethylamine salt; and mixed C1018 normal primary alkyl triethenoxy sulphate, potassium salt.
Other useful anionic detergents include the higher acyl sarcosinates, e.g. sodium N-lauroyl sarcosinate; higher fatty alcohol sulphates, such as sodium lauryl sulphate and sodium tallow alcohol sulphate; sulphated oils; sulphates of mono- or di-glycerides of higher fatty acids, e.g.
stearic mono-glyceride monosulphate; although, of these, the sodium higher alcohol sulphates have been found to be inferior to the polyethoxylated sulphates in detergency; aromatic poly(lower alkenoxy) ether sulphates, such as the sulphates of the condensation products of ethylene oxide and nonyl phenol (usually having 1 to 20 oxyethylene groups per molecule, preferably 2 to 12); polyethoxy higher alcohol sulphates and alkyl phenol polyethoxy sulphates having a lower alkoxy (of 1 to 4 carbon atoms, e.g. methoxy) substituent on a carbon close to that carrying the sulphate group, such as monomethyl ether monosulphate of a long chain vicinal glycol, e.g. mixture of vicinal alkane diols of 1 6 to 20 carbon atoms in a straight chain; acyl esters of isethionic acid, e.g. oleyl taurides; higher alkyl phenyl polyethoxy sulphonates; higher alkyl phenyl polyethoxy sulphonates; higher alkyl phenyl di-sulphonates, e.g. pentadecyl phenyl disulphonate; and higher fatty acid soaps, e.g. mixed coconut oil and tallow soaps in a
1:4 ratio.
Among the aforementioned types of anionic detergents, the sulphates and sulphonates are generally preferred but the corresponding organic phosphates and phosphonates may also be employed when their contents of phosphates are not objectionable. Generally, the water soluble anionic synthetic organic detergents, (including soaps), are salts of alkali metal cations, such as potassium, lithium, and especially sodium, although salts of ammonium and substituted ammonium cations, such as those previously described , e.g. triethanolamine, triisopropylamine, may also be used.
A nonionic detergent may optionally be employed in minor amounts to supplement the aniionic detergent compound in the built liquid detergent compositions of the present invention.
When used in such combination with an anionic detergent, the amount of nonionic detergent will generally be below about 10%, and preferably below about 5%, by weight, of the total composition.
The nonionic detergents are usually poly-lower alkoxyiated lipophiles wherein the desired hydrophile-lipophile balance is obtained from addition of a hydrophilic poly-lower alkoxy group to a lipophilic moiety. For the compositions of the present invention the nonionic detergent employed is preferably a poly-lower alkoxylated higher alkanol wherein the alkanol is of 10 to 1 8 carbon atoms and wherein the number of moles of lower alkylene oxide (of 2 or 3 carbon atoms) is from 3 to 1 2. Of such materials it is preferred to employ those wherein the higher alkanol is a higher fatty alcohol of 11 or 1 2 to 1 5 carbon atoms and which contain from 5 to 8 or 9 lower alkoxy groups per mole.Preferably, the lower alkoxy group is an ethoxy group but in some instances it may be desirably mixed with propoxy groups, the latter, if present, usually being a minor (less than 50%) constituent. Exemplary of such compounds are those wherein the alkanol is of 1 2 to 1 5 carbon atoms and which contain about 7 ethylene oxide groups per mole, e.g. Neodol (Registered Trade Mark) 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 about 1 2 to 1 5 carbon atoms, with about 7 moles of ethylene oxide and the latter is a corresponding mixture wherein the carbon atoms content of the higher fatty alcohol is 12 to 1 3 and the number of ethylene oxide groups per mole averages about 6.5. The higher alcohols are primary alkanols. Other examples of such detergents include Tergitol (Registered
Trade Mark) 15-S-7 and Tergitol 15-S-9, both of which are linear secondary alcohol ethoxylates made by Union Carbide Corporation.The former is a mixed ethoxylation product of an 11 to 1 5 carbon atom 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.
Also useful in the present compositions 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 1 5 carbon atoms and the number of ethylene oxide groups per mole being about 11. Such products are also made by Shell Chemical Company.
Other useful nonionics are represented by Plurafac B-26 (BASF Chemical Company), the reaction product of a higher linear alcohol and a mixture of ethylene and propylene oxides.
In the preferred poly-lower alkoxylated higher alkanols, the best balance of hydrophilic and lipophilic moieties are obtained when the number of lower alkoxy groups are from about 40% to 100% of the number of carbon atoms in the higher alcohol, preferably 40 to 60% thereof. The nonionic detergent is preferably comprised of at least 50% of the preferred ethoxylated alkanols.
Higher molecular weight alkanols and various other normally solid nonionic detergent compounds and surfactants may contribute to gelation of the liquid detergent composition and consequently, are normally omitted or limited in quantity in the compositions of the present invention, although minor proportions thereof may be employed for their cleaning properties, etc. With respect to both preferred and less preferred nonionic detergents, the alkyl groups present therein are preferably linear although minor degrees of slight branching may be tolerated, such as at a carbon next to or two carbons removed from the terminal carbon of the straight chain and away from the ethoxy chain with the proviso that such branched alkyl group is no more than three carbon atoms in length.Normally the proportion of carbon atoms in such a branched configuration will be minor, rarely exceeding 20% of the total carbon atom content of the alkyl group. Similarly, although linear alkyl groups which are terminally joined to the ethylene oxide chains are highly preferred and are considered to result in the optimum combination of detergency, biodegradability and non-gelling characteristics, medial or secondary joiner to the ethylene oxide in the chain may occur. In such instance, it is usually in only a minor proportion of such alkyl groups, generally less than 20% but as is in the case of the aforementioned Tergitols, may be greater. Also, when propylene oxide is present in the lower alkylene oxide chain, it will usually be less than 20% thereof and preferably less than 10% thereof.
The non-phosphate detergent builder salts are employed in the present compositions in amounts of from about 5 to 25%, and preferably from about 1 to 20%, by weight. Specific examples of non-phosphorous water-soluble inorganic builders include water-soluble inorganic carbonate, bicarbonate and silicate salts. The alkali metal, for example, sodium and potassium, carbonates, bicarbonates and silicates are particularly useful herein.
Water-soluble organic builders are also useful and include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxysulphonates. Specific examples of polyacetate and polycarboxylate builders include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylene diaminetetracetic acid, nitrilotriacetic acid, benzene polycarboxylic (i.e. penta- and tetra-) acids, carboxymethoxysuccinic acid and citric acid.
The percentage of water, the main solvent in the present compositions, will usually be from about 25 to 75%, preferably 40 to 60%, by weight, of the liquid composition.
The optical fluorescent brighteners or whiteners usually employed in liquid detergent compositions are important constituents of modern detergent compositions which give washed laundry and materials a bright appearance so that the laundry is not only clean but also appears clean. Although it is possible to utilize a single brightener for a,specific intended purpose in the liquid detergent compositions of the present invention it is generally desirable to employ mixtures of brighteners which will have good brightening effects on cotton, nylons, polyesters and blends of such materials and which are also bleach stable. A good description of such types of optical brighteners is given in the article "The Requirements of Present Day Detergent
Fluorescent Whitening Agents" by A.E. Siegrist, J. Am. Oil Chemists Soc., January 1978 (Vol.
55). That article and U.S. Patent 3,812,041, issued 21st May, 1974, both of which are hereby incorporated by reference contain detailed descriptions of a wide variety of suitable optical brighteners.
Among the brighteners that are useful in the present liquid detergent compositions are:
Calcofluor 5BM (American Cyanamid); Calcofluor White ALF (American Cyanamid); SOF
A-2001 (Ciba); CDW (Hilton-Davis); Phorwite RKH, Phorwite BBH and Phorwite BHC (Verona);
CSL, powder, acid (American Cyanamid); FB 766 (Verona); Blancophor PD (GAF); UNPA (Geigy); Tinopal RBS 200 (Geigy).
Adjuvants may be present in the liquid detergent compositions to provide additional properties, either functional or aesthetic. Included among the useful adjuvants are soil suspending or antiredeposition agents, such as polyvinyl alcohol, sodium carboxymethyl cellulose, hydroxypropylmethyl cellulose; thickeners, e.g. gums, alginates, agar agar; foam improvers, e.g. lauric myristic diethanolamide; foam destroymers, e.g. silicones; bactericides, e.g. tribromosalicylanilide and hexachlorophene; dyes; pigments (water dispersible); preservatives; ultra-violet absorbers; fabric softeners; opacifying agents, e.g. polystyrene suspensions;
and perfumes. Of course, such materials will be selected based on the properties desired in the finished product, their compatibility with the other constituents, and their solubility in the liquid composition.
The present liquid compositions are efficient and easy to use. Compared to heavy duty
laundry detergent powders, much smaller volumes of the present liquids may be employed to obtain comparable cleaning of soiled laundry. For example, using a typical preferred formulation of the present invention, only about 1 32 grams or 1/2 cup of liquid is needed for a full tub of wash in a top-loading automatic washing machine in which the water volume is 1 5 to 1 8 gallons (55 to 75 litres); and even less is needed for front-loading machines. Thus, the concentration of the liquid detergent composition in the wash water is on the order of about 0.2%. Usually, the proportion of the liquid composition in the wash solution will range from about 0.05 to 0.3%, preferably from 0.15 to 0.25%.The proportions of the various
constituents of the liquid composition may vary accordingly. Equivalent results can be obtained
by using greater proportions of a more dilute formulation but the greater quantity needed will
require additional packaging and will generally be less convenient for consumer use.
The invention may be put into practice in varous ways and a number of specific embodiments will be described to illustrate the invention with reference to the accompanying examples.
EXAMPLES 1A to 1E Enzyme-containing built liquid detergent compositions were formulated as set forth in Table 1.
The values shown indicate weight percent. Examples 1 A and 1 B are comparison examples.
TABLE 1
Example 1A 1B 1 1D 1E Ingredient
Sodium dodecylbenzene
sulphonate 7 7 7 7 7
Ethoxylated C,2-C,s alcohol
sulphate (3 mole EO/mole
alcohol) ( 7 7 7 7 7
Brightener 0.2 0.2 0.2 0.2 0.2
Sodium Nitrilotriacetate 15 15 15 15 15
PBB2 1 1 1 1 1
Perfume 0.3 0.3 0.3 0.3 0.3
Protease enzyme (3) 1 1 1 1 1 Propylene glycol - 20 20 20 20
Borax - - 1 2 3
Water balance
Percent active enzyme after (a)4 days at 110"F(43"C) - - - - 98% (b) 6 days at 110"F(43"C) 0 15 61 86 88
Notes on Table 1:
(1) Neodol 25-3S sold by Shell Oil Company.
(2) Polar Brilliant Blue - a 1% active dye solution.
(3) "Esperase" sold by Novo Industries containing 5% enzyme, 75% propylene glycol, and balance water having an activity of 8.0 KNPU/gm. (Kilo Novo Protease units/gm).
The enzyme activities of the compositions of Examples 1 A to 1 E were tested after 6 days storage at 110 F (43 C), the percent activity relative to the initial value being indicated in Table 1. The activity after 4 days was measured only for the composition of Example 1C. The compositions of Examples 1 A and 1 B were the only compositions which did not contain an enzyme stabilizing system in accordance with the present invention, and manifested a total (Example 1A) or near total (Example 1 B) loss of enzyme activity after 6 days. The compositions of Examples 1C, 1 D and 1 E reflect the marked improvement of enzyme stability attendant on the inclusion of propylene glycol and borax in the detergent composition.
The compositions of Exampes 1 B to 1 E were all clear, single-phase, homogeneous solutions which maintained their physical stability and clarity after 6 months of storage at both room temperature and at 110 F (43 C). The composition of Example 1A which was not in accordance with the invention was physically unstable due to the absence of propylene glycol which in addition to serving as an enzyme stabilizer (in conjunction with the aforementioned boron compound) promotes the solubility of the anionic detergents and the NTA builder in the aqueous composition.
EXAMPLES 2A and 2B
Example 2A is a comparison example. Enzyme-containing built liquid detergent compositions (Examples 2A and 2B) were formulated essentially similarly to the compositions of Examples 1A to 1 E except that sodium citrate was used as the builder salt instead of sodium NTA. The ingredients are shown below in Table 2, and the amounts are weight percentages.
TABLE 2
Example 2A 2B
Ingredient
Sodium dodecyl benzene sulphonate 7 7
Ethoxylated C,2-C,5 alcohol sulphate
( 3 moles EO/mole alcohol) 7 7
Brightener 0.2 0.2
Sodium citrate 12 12 PBB1 1 1 Perfume 0.3 0.3
Protease enzyme(2) 1 1 Propylene glycol 20 20
Borax - 2
Water balance
Percent active enzyme after 4 days at 110"F(43"C) 20 95
Notes of Table 2:
(1) Polar Brilliant Blue a 1% active dye solution.
(2) "Esperase" sold by Novo Industries contaning 5% enzyme, 75% propylene glycol, and balance water having an activity of 8.0 KNPU/gm. (Kilo
Novo Protease units/gm).
The composition of Example 2B in accordance with the present invention manifested an enzyme activity after four days of 95% as compared to the composition of Example 2A which contained no boron compound and consequently lost more than 75% of its initial enzyme activity.
Both compositions were clear single-phase solutions which remained physically stable after six months of storage at both room temperature and 110 F (43 C).
EXAMPLES 3A to 3C
Example 3A is a comparison Example. Enzymecontaining built liquid detergent compositions (Examples 3A to 3C) were formulated essentially similarly to the compositions of Example 2 except that they contained a mixture of protease and alphaamylase enzymes instead of a single protease enzyme. The ingredients are shown in Table 3 and the amounts are in weight percent.
TABLE 3
Example 3A 3B 3C
Ingredient
Sodium dodecyl benzene sulphonate 7 7 7
Ethoxylated C,2-C15 alcohol sul
phate (3 moles EO/mle alcohol) 7 7 7
Brightener 0.2 0.2 0.2
Sodium citrate 12 12 12 PBB(1 1 1 1 Perfume 0.3 0.3 0.3
Protease enzyme(2) 1 1 1 amylase enzyme3) 0.4 0.4 0.4
Propylene glycol 20 20 20
Borax - 1 3
Water balance
Percent active enzyme after 4 days
at 100"F (43"C) a-amylase enzyme 50% 67% 87%
Protease enzyme 30 73 94
Notes on Table 3:
(1) Polar Brilliant Blue a 1% active dye solution.
(2) "Esperase" sold by Novo Industries containing 5% enzyme, 75% propylene glycol, and balance water having an activity of 8.0 KNPU/gm. (Kilo Novo Protease units/gm).
(3) "Termamyl" sold by Novo Industries containing 5% enzyme, 18% sodium chloride and balance water having an activity of 120,000 Novo amylase units per gram.
The compositions of Examples 3B and 3C in accordance with the present invention demonstrated a markedly more stable enzyme activity after four days for both the protease and amylase enzymes relative to the composition of Example 3A which contained no boron compound and consequently lost about 50% of its initial amylolytic activity and about 33% of its initial proteolytic activity during the period of four days.
All three compositions were clear single-phase solutions which remained physically stable after six months of storage.
Claims (10)
1. A stabilized aqueous, built, clear, single-phase, enzyme-containing liquid detergent composition comprising:
(a) from about 8 to 20%, by weight, of one or more surface active anionic detergent compounds;
(b) from about 5 to 25%, by weight, of a water-soluble non-phosphate detergent builder salt;
(c) an effective amount of an enzyme of enzyme mixture selected from the group consisting of alkaline protease enzymes and alpha-amylase enzymes;
(d) an enzyme stabilizing system containing, based on the weight of the detergent composition, (i) from about 1 2 to 25% of propylene glycol and (ii) from about 1 to 5% of a boron compound consisting of boric acid, boric oxide or an alkali metal borate or mixtures thereof; and
(e) from about 25 to 75% by weight of water.
2. A detergent composition as claimed in Claim 1 in which the said builder salt comprises sodium citrate.
3. A detergent composition as claimed in Claim 1 or Claim 2 in which the said builder salt comprises sodium nitrilotriacetate.
4. A detergent composition as claimed in Claim 1, 2 or 3 which is substantially free of a phosphate detergent builder salt.
5. A detergent composition as claimed in any one of Claims 1 to 4 which contains from about 1 5 to 20%, by weight, of propylene glycol and from about 1 to 3%, by weight, of the said boron compound.
6. A detergent composition as claimed in any one of Claims 1 to 5 in which the said boron compound comprises borax.
7. A detergent composition as claimed in any one of Claims 1 to 6 in which the said builder salt is present in an amount of from about 10 to 20%, by weight.
8. A detergent composition as claimed in any one of Claims 1 to 7 in which the anionic detergent is a mixture of a C10-C,8 alkyl benzene sulphonate salt and a polyethoxylated C10-C,8 alcohol sulphate salt.
9. A detergent composition as claimed in Claim 1 substantially as specifically described herein with reference to Example 1 C, 1 D or 1 E, 2B or 2C or 38 or 3C.
10. A method of laundering comprising contacting the stained and/or soiled fabrics to be laundered with an enzyme-containing, built, clear single-phase liquid detergent composition as claimed in any one of Claims 1 to 9.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
MYPI87002251A MY102605A (en) | 1983-05-31 | 1987-09-29 | Built single-phase liquid anionic detergent composition containing stabilized enzymes. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49964583A | 1983-05-31 | 1983-05-31 |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8413673D0 GB8413673D0 (en) | 1984-07-04 |
GB2140819A true GB2140819A (en) | 1984-12-05 |
GB2140819B GB2140819B (en) | 1987-06-24 |
Family
ID=23986099
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08413673A Expired GB2140819B (en) | 1983-05-31 | 1984-05-29 | Built single-phase liquid anionic detergent composition containing stabilized enzymes |
Country Status (25)
Country | Link |
---|---|
AT (1) | AT394385B (en) |
AU (1) | AU558722B2 (en) |
BE (1) | BE899778A (en) |
BR (1) | BR8402593A (en) |
CA (1) | CA1220741A (en) |
CH (1) | CH660374A5 (en) |
DE (1) | DE3418294A1 (en) |
DK (1) | DK159881C (en) |
FR (1) | FR2546902B1 (en) |
GB (1) | GB2140819B (en) |
GR (1) | GR82007B (en) |
HK (1) | HK67490A (en) |
IE (1) | IE58061B1 (en) |
IT (1) | IT1177762B (en) |
LU (1) | LU85392A1 (en) |
MX (1) | MX162796A (en) |
MY (1) | MY102605A (en) |
NL (1) | NL8401740A (en) |
NO (1) | NO160451C (en) |
NZ (1) | NZ208156A (en) |
PH (1) | PH19081A (en) |
PT (1) | PT78653B (en) |
SE (1) | SE8402869L (en) |
SG (1) | SG44890G (en) |
ZA (1) | ZA843665B (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4537706A (en) * | 1984-05-14 | 1985-08-27 | The Procter & Gamble Company | Liquid detergents containing boric acid to stabilize enzymes |
US4537707A (en) * | 1984-05-14 | 1985-08-27 | The Procter & Gamble Company | Liquid detergents containing boric acid and formate to stabilize enzymes |
EP0181041A2 (en) * | 1984-11-09 | 1986-05-14 | The Procter & Gamble Company | Ethanol-free liquid laundry detergent compositions |
US4842758A (en) * | 1986-10-31 | 1989-06-27 | Colgate-Palmolive Company | Stabilized enzyme system for use in aqueous liquid built detergent compositions |
US4842769A (en) * | 1985-07-26 | 1989-06-27 | Colgate-Palmolive Co. | Stabilized fabric softening built detergent composition containing enzymes |
EP0344828A2 (en) * | 1988-05-06 | 1989-12-06 | Unilever N.V. | Liquid detergent compositions |
EP0348183A2 (en) * | 1988-06-23 | 1989-12-27 | Unilever Plc | Enzyme-containing liquid detergents |
US4900475A (en) * | 1985-07-26 | 1990-02-13 | Colgate-Palmolive Co. | Stabilized built liquid detergent composition containing enzyme |
EP0381262A2 (en) * | 1989-01-30 | 1990-08-08 | Unilever N.V. | Enzymatic liquid detergent composition |
EP0401661A1 (en) * | 1989-06-08 | 1990-12-12 | Henkel Kommanditgesellschaft auf Aktien | Liquid enzyme concentrate |
WO1991000333A1 (en) * | 1989-07-03 | 1991-01-10 | Henkel Kommanditgesellschaft Auf Aktien | Enzymatic cleaner |
WO1991009929A1 (en) * | 1989-12-22 | 1991-07-11 | Henkel Kommanditgesellschaft Auf Aktien | Stabilizers for aqueous cleaning fluids |
US5089163A (en) * | 1989-01-30 | 1992-02-18 | Lever Brothers Company, Division Of Conopco, Inc. | Enzymatic liquid detergent composition |
WO1992005238A1 (en) * | 1990-09-17 | 1992-04-02 | The Procter & Gamble Company | Liquid detergent compositions |
EP0481663A1 (en) * | 1990-10-15 | 1992-04-22 | E.R. Squibb & Sons, Inc. | Combined two stage method for cleaning and decontaminating surgical instruments |
FR2680372A1 (en) * | 1991-08-16 | 1993-02-19 | Sandoz Sa | STABLE AQUEOUS PREPARATIONS OF ENZYMES AND THEIR USE. |
WO1993011215A1 (en) * | 1991-12-04 | 1993-06-10 | The Procter & Gamble Company | Liquid laundry detergents with citric acid, cellulase, and boric-diol complex to inhibit proteolytic enzyme |
US5318715A (en) * | 1991-05-31 | 1994-06-07 | Colgate-Palmolive Company | Liquid automatic dishwashing composition containing two enzymes |
US5468414A (en) * | 1991-04-30 | 1995-11-21 | Panandiker; Rajan K. | Built liquid detergents with boric-polyol complex to inhibit proteolytic enzyme |
US5618465A (en) * | 1991-05-31 | 1997-04-08 | Colgate Palmolive Co. | Nonaqueous liquid automatic dishwashing composition containing enzymes |
EP1067176A1 (en) * | 1999-07-06 | 2001-01-10 | Mifa Ag Frenkendorf | Liquid portionable water-free detergent concentrate |
WO2002024851A1 (en) * | 2000-09-20 | 2002-03-28 | Reckitt Benckiser Inc. | Aqueous compositions comprising protease and/or amylase |
WO2004003123A3 (en) * | 2002-06-28 | 2004-04-22 | Reckitt Benckiser Nv | Detergent composition |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ216792A (en) * | 1985-07-26 | 1989-04-26 | Colgate Palmolive Co | Stabilised,fabric-softening built detergent compositions containing enzymes and swelling bentonite clay |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2079305A (en) * | 1980-07-02 | 1982-01-20 | Unilever Plc | Liquid enzyme detergent |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI61715C (en) * | 1976-11-01 | 1982-09-10 | Unilever Nv | ENZYMER INNEHAOLLANDE STABILIZERAD FLYTANDE DETERGENTKOMPOSITION |
US4261868A (en) * | 1979-08-08 | 1981-04-14 | Lever Brothers Company | Stabilized enzymatic liquid detergent composition containing a polyalkanolamine and a boron compound |
DE3264685D1 (en) * | 1981-11-13 | 1985-08-14 | Unilever Nv | Enzymatic liquid cleaning composition |
US4462922A (en) * | 1981-11-19 | 1984-07-31 | Lever Brothers Company | Enzymatic liquid detergent composition |
NL8202294A (en) * | 1982-06-07 | 1984-01-02 | Chem Y | LIQUID PHOSPHATE-FREE DETERGENT. |
-
1984
- 1984-05-14 NZ NZ208156A patent/NZ208156A/en unknown
- 1984-05-15 ZA ZA843665A patent/ZA843665B/en unknown
- 1984-05-17 AU AU28318/84A patent/AU558722B2/en not_active Ceased
- 1984-05-17 DE DE3418294A patent/DE3418294A1/en not_active Ceased
- 1984-05-23 CH CH2564/84A patent/CH660374A5/en not_active IP Right Cessation
- 1984-05-24 FR FR8408170A patent/FR2546902B1/en not_active Expired
- 1984-05-28 SE SE8402869A patent/SE8402869L/en not_active Application Discontinuation
- 1984-05-28 PT PT78653A patent/PT78653B/en not_active IP Right Cessation
- 1984-05-29 IT IT48275/84A patent/IT1177762B/en active
- 1984-05-29 BE BE0/213025A patent/BE899778A/en not_active IP Right Cessation
- 1984-05-29 GB GB08413673A patent/GB2140819B/en not_active Expired
- 1984-05-30 LU LU85392A patent/LU85392A1/en unknown
- 1984-05-30 DK DK269084A patent/DK159881C/en not_active IP Right Cessation
- 1984-05-30 BR BR8402593A patent/BR8402593A/en not_active IP Right Cessation
- 1984-05-30 NO NO842163A patent/NO160451C/en unknown
- 1984-05-30 GR GR74869A patent/GR82007B/el unknown
- 1984-05-30 PH PH30741A patent/PH19081A/en unknown
- 1984-05-30 AT AT0178384A patent/AT394385B/en not_active IP Right Cessation
- 1984-05-30 IE IE134784A patent/IE58061B1/en not_active IP Right Cessation
- 1984-05-30 NL NL8401740A patent/NL8401740A/en not_active Application Discontinuation
- 1984-05-30 CA CA000455401A patent/CA1220741A/en not_active Expired
- 1984-05-31 MX MX201516A patent/MX162796A/en unknown
-
1987
- 1987-09-29 MY MYPI87002251A patent/MY102605A/en unknown
-
1990
- 1990-06-22 SG SG44890A patent/SG44890G/en unknown
- 1990-08-30 HK HK674/90A patent/HK67490A/en unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2079305A (en) * | 1980-07-02 | 1982-01-20 | Unilever Plc | Liquid enzyme detergent |
Cited By (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4537707A (en) * | 1984-05-14 | 1985-08-27 | The Procter & Gamble Company | Liquid detergents containing boric acid and formate to stabilize enzymes |
US4537706A (en) * | 1984-05-14 | 1985-08-27 | The Procter & Gamble Company | Liquid detergents containing boric acid to stabilize enzymes |
EP0181041A2 (en) * | 1984-11-09 | 1986-05-14 | The Procter & Gamble Company | Ethanol-free liquid laundry detergent compositions |
EP0181041A3 (en) * | 1984-11-09 | 1988-01-27 | The Procter & Gamble Company | Ethanol-free liquid laundry detergent compositions |
US4842769A (en) * | 1985-07-26 | 1989-06-27 | Colgate-Palmolive Co. | Stabilized fabric softening built detergent composition containing enzymes |
US4900475A (en) * | 1985-07-26 | 1990-02-13 | Colgate-Palmolive Co. | Stabilized built liquid detergent composition containing enzyme |
US4842758A (en) * | 1986-10-31 | 1989-06-27 | Colgate-Palmolive Company | Stabilized enzyme system for use in aqueous liquid built detergent compositions |
EP0344828A3 (en) * | 1988-05-06 | 1990-07-18 | Unilever N.V. | Liquid detergent compositions |
EP0344828A2 (en) * | 1988-05-06 | 1989-12-06 | Unilever N.V. | Liquid detergent compositions |
EP0348183A3 (en) * | 1988-06-23 | 1991-05-29 | Unilever Plc | Enzyme-containing liquid detergents |
EP0348183A2 (en) * | 1988-06-23 | 1989-12-27 | Unilever Plc | Enzyme-containing liquid detergents |
EP0381262A3 (en) * | 1989-01-30 | 1991-07-31 | Unilever N.V. | Enzymatic liquid detergent composition |
EP0381262A2 (en) * | 1989-01-30 | 1990-08-08 | Unilever N.V. | Enzymatic liquid detergent composition |
US5089163A (en) * | 1989-01-30 | 1992-02-18 | Lever Brothers Company, Division Of Conopco, Inc. | Enzymatic liquid detergent composition |
EP0401661A1 (en) * | 1989-06-08 | 1990-12-12 | Henkel Kommanditgesellschaft auf Aktien | Liquid enzyme concentrate |
WO1990015129A1 (en) * | 1989-06-08 | 1990-12-13 | Henkel Kommanditgesellschaft Auf Aktien | Fluid enzyme concentrate |
WO1991000333A1 (en) * | 1989-07-03 | 1991-01-10 | Henkel Kommanditgesellschaft Auf Aktien | Enzymatic cleaner |
WO1991009929A1 (en) * | 1989-12-22 | 1991-07-11 | Henkel Kommanditgesellschaft Auf Aktien | Stabilizers for aqueous cleaning fluids |
WO1992005238A1 (en) * | 1990-09-17 | 1992-04-02 | The Procter & Gamble Company | Liquid detergent compositions |
EP0481663A1 (en) * | 1990-10-15 | 1992-04-22 | E.R. Squibb & Sons, Inc. | Combined two stage method for cleaning and decontaminating surgical instruments |
US5468414A (en) * | 1991-04-30 | 1995-11-21 | Panandiker; Rajan K. | Built liquid detergents with boric-polyol complex to inhibit proteolytic enzyme |
US5618465A (en) * | 1991-05-31 | 1997-04-08 | Colgate Palmolive Co. | Nonaqueous liquid automatic dishwashing composition containing enzymes |
US5318715A (en) * | 1991-05-31 | 1994-06-07 | Colgate-Palmolive Company | Liquid automatic dishwashing composition containing two enzymes |
FR2680372A1 (en) * | 1991-08-16 | 1993-02-19 | Sandoz Sa | STABLE AQUEOUS PREPARATIONS OF ENZYMES AND THEIR USE. |
WO1993011215A1 (en) * | 1991-12-04 | 1993-06-10 | The Procter & Gamble Company | Liquid laundry detergents with citric acid, cellulase, and boric-diol complex to inhibit proteolytic enzyme |
CN1040019C (en) * | 1991-12-04 | 1998-09-30 | 普罗格特-甘布尔公司 | Liquid detergent for washing clothes containing cellulosic enzyme by inhibiting albumen hydrolytic enzyme |
EP1067176A1 (en) * | 1999-07-06 | 2001-01-10 | Mifa Ag Frenkendorf | Liquid portionable water-free detergent concentrate |
CH695688A5 (en) * | 1999-07-06 | 2006-07-31 | Mifa Ag Frenkendorf | Liquid Portionable anhydrous detergent concentrate. |
WO2002024851A1 (en) * | 2000-09-20 | 2002-03-28 | Reckitt Benckiser Inc. | Aqueous compositions comprising protease and/or amylase |
US7119054B2 (en) | 2000-09-20 | 2006-10-10 | Reckitt Benckiser Inc | Aqueous compositions comprising protease and/or amylase |
WO2004003123A3 (en) * | 2002-06-28 | 2004-04-22 | Reckitt Benckiser Nv | Detergent composition |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19940529 |