IE861974L - Liquid detergent composition containing enzymes - Google Patents

Abstract

A stabilized enzyme-containing liquid detergent comprises (a) 5 to 20%, a non-cationic surface active detergent compound (b) 5 to 30%, of a builder salt; (c) 5 to 20%, of a swelling bentonite clay; (d) an effective amount of an enzyme of; (e) an enzyme-stabilizing system containing, based on the weight of the detergent composition, (i) 1% to 10% glycerine; (ii) 1 to 8% of boric acid, boric oxide or an alkali metal borate; and (iii) 0.5 to 8% of a of mono, di and/or polycarboxylic acid having 1 to 8 carbon atoms or a water-soluble salt thereof; and (f) water. e [GB2178055A]

Description

*'6 in PJL2S15 - la - "STABILIZED BUILT LIQUID DETERGENT COMPOSITION containING enzymes" J b The present invention relates to stable, built, enayaie-containing liquid detergent compositions suitable for laundry or pre-soa)c formulations. More particularly, the present invention relates to 5„ aqueous enzyme-containing liquid detergent compositions vjhich contain one or more detergent builders and which are characterised by being physically stable, homogeneous liquid compositions.

The formulation of stabilised e n. sv me - c o n. t a i n, i ng 10. 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 ansymes in decomposing proteiuaceous and 15. 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, ensymatic materials suitable for laundry compositions, particularly 20. proteolytic enzymes, are relatively expensive.

Indeed, they generally are among the most expensive ingredients in a typical commercial liquid detergent composition,, even though they are present in relatively minor amounts. Moreover, enzymes are known to 25. be unstable in aqueous compositions. It is for this reason that an excess of enzymes is generally required in liquid detergent formulations to t compensate for the expected loss of ensvme activity during prolonged periods of storage» Accordingly, the t „ prior art is replete with suggestions for stabilising P12915 2. ensyme-containing liquid detergent compositions, and in particular unbuilt liquid compositions by the use of various materials which are incorporated into the composition to function as enzyme stabilisers.

In the case of liquid detergent compositions containing a builder, the problem of ensyiae instability is particularly acute. Primarily this is because detergent builders have a destabilising effect on enzymes, even in compositions containing ensyme stabilisers 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 composition; the solubility of sodium tripolvphosphate, for example,, being relatively limited in aqueous compositions, and especially in the presence of anionic and nonionic detergents.

In o.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» As noted in the examples of the u.k. application, relatively large amounts of glycerol are required to stabilise the ensymes in the composition. Yet, as demonstrated hereinafter in the present specification, the ensyme stabilising effect provided by a mixture of glycerine and borax in a built aqueous liquid detergent composition is relatively modest.

In European Patent Application Publication Ho„ P12915 3. 0125505, there is disclosed an aqueous ensyme-containing liquid detergent composition containing an enzyme stabilising mixture consisting of certain dicarboxylic acids and borax. The dicarboxylic acids 5„ are recommended as a substitute for a polyol such as glycerol in known enzyme stabilizing mixtures consisting of glycerol and a boron compound.

However, the dicarboxylic acid-borax mixtures of this publication in common with the aforementioned prior 10,. art.mixture of glycerine and borax are incapable of providing anything other than a modest stabilizing effect in the present built liquid detergent compositions .

The present invention provides a stabilized 15. fabric softening„ ensyme-containing built liquid detergent composition comprising: (a) from about 5 to 20%, by weight, of one or more surface active detergent compounds selected from the group consisting of anionic, nonionic and ampho- , teric detergent compounds; (b) from about 5 to 30%, by weight, of one or more builder salts selected from the group consisting of alkali metal tripolyphosphates, alkali metal carbonates, alkali metal nitrilotriacetates, and poly- . acetal carboxvlates; (c) from about 5 to 20%, by weight, of a swelling bentonite clay, .

P12 815 4. (d) an effective amount of an enzyme or an enzyme mixture selected from the group consisting of alkaline protease enzymes and alpha-amylase enzymes; (e) an enzyme-stabilising system containing, . based on the weight of the detergent composition, (i) from about 1 to 10% glycerine; (ii) from about 1 to 8% of a boron compound selected from the group consisting of boric acid, boric oxide and alkali metal borates and; (iii) from about 0.5 to 8% of a 10. carboxylic acid compound selected from the group consisting of mono, di and/or polycarboxvlic acids having 1 to 8 carbon atoms and water-soluble salts thereof; and (f) the balance comprising water and optionally 15. perfume and other adjuvants.

In a preferred embodiment of the present invention, the liquid detergent composition comprises (a) from about 5 to 15% of an alkali metal alkyl-benzene sulphonate wherein the alkyl group contains . 12 to 15 carbon atoms; (b) from about 2 to 5% of an alkali metal alkyl polysthoxy sulphate wherein the alkyl group contains to 18 carbon atoms and the polyethoxv is of 3 to 11 ethylene oxide groups,, the weight ratio of (a) to 25. (b) being from about 2:1 to about 8:1; (c) from about 5 to 20% of sodium tripolyphos-phate; (d) from about 1 to 10% of sodium carbonate, the weight ratio of (c) to (d) being from about 2s1 to . about 6si; P12S15 (a) from about 10 to 15% of a sodium bentonite; (£) an effective amount of the aforesaid enzyme or enzyme mixture; (g) an ensyme stabilising system containing, . basad on the weight of the detergent composition, (i) from about 3 to 7% glycerine, (ii) from about 1 to 5% of an alkali metal borate and (iii) from about 0.5 to 4% of the said carboxylic acid compound; and (h) the balance comprising Mater and optionally 10. perfume and other adjuvants.

In accordance with the process of the present invention, laundering of stained and/or soiled materials is affected by contacting such materials with an aqueous solution of the above-defined liquid 15. detargent compositions.

The described liquid detergent is a commercially acceptable heavy duty laundry detergent f capable of satisfactorily cleaning laundry itesns containing both oily and particulate soils- Additionally, the 20. described compositions may be employed for the pre-treatment of badly soiled areas, such as collars and cuffs, of items to be laundered.

The present invention is predicated upon the discovery of & three component enzyme stabilising 25. system as herein defined which provides an enzyme stabilising effect to the liquid detergent compositions of the present invention far in excess of that which can be achieved with conventional enzyme stabilisers. The enzyme stabilising effect thus 30. achieved reflects a synergy among the three components. In accordance with the present invention, the ensyme stability provided by a mixture of glycerine and borax or a mixture of borax and a P12915 dicarboxylic acid as disclosed in the prior art can be synergistically improved by the use of the three component stabilising system herein defined in the present liquid compositions so as to raise the level 5. of enzyme stability significantly above that provided by either the mixture of glycerine and borax or the mixture of borax and dicarboxylic acid when used independently of each other as snsvme stabilisers. For commercial purposes, a desirable ensvme stability 10. generally corresponds to about a half-life of one week at a temperature of 110°F (43°C).

The ensyme stabilising system of the present invention is a mixture of glycerine, a boron compound selected from among boric acid f boric oxide and an 15. alkali metal borate and a carboxylic acid compound as herein defined. The weight of the stabilising system in the present built liquid detergent compositions is generally from about 3 to 25%, preferably about 6 to 15%, by weight„ The weight ratio of glycerine to 20. borax in the stabilising mixtures is generally from about 1 to 3. The preferred amount of glycerine in the composition is from about 1 to 5%, and the preferred amount of carboxylic compound is from about 0„5 to 4% based on the weight of the composition-25. The carboxylic acid compounds which are useful in the ensyme stabilising system of the present invention encompass saturated as well as unsaturated mono, di and polycarboxylic acids having 1 to 8 carbon atoms among which are included oxalic acid 30. (HOOCCOOH), malonic acid (hoocch2cooh), maleic acid P12915 (HOOCCH:CHCOOH) and succinic acid (HOOCCH2CH2COOH)» The carboxylic acids may contain hydroxy or amino substituents as exemplified by malic acid (hqocchohch2cooh), tartaric acid (dihydroxysuccinic 5. acid) aspartic acid (amino succinic acid) and citric acid. Preferred carboxylic acids of the present invention are aspartic acid, tartaric acid, maIonic acid and malic acid. From a commercial standpoint, a particularly preferred carboxylic acid compound is 10. citric acid and/or its salts because of their relatively low cost.

The alkaline proteolytic snsymes suitable for the compositions of the present invention include the various commercial liquid enzyjae preparations which 15. have beer, adapted for use in detergent compositions. Ensyme preparations in powdered form are also useful although, as a general rule, less convenient for incorporation into the built liquid detergent compositions. Thus, suitable liquid enssysae preparations 20. include "Alcalase" and "Esperase" sold by Novo Industries, Copenhagen,, Denmark, and "Maxatase" and "Ag-Protease" sold by Gist-Brocades, Delft, The Netherlands.

Among the suitableK-amylase liquid enzyme 25. preparations are those sold by Sovo Industries and Gist-Brocades under the tradenames "Termaiayl'0 and Maxamyl", respectively.

"Esperase" is particularly preferred for the present compositions because of its optimized 30. activity at the higher pH values corresponding to the built detergent compositions.

P12915 8.

The preferred detergents for use in the present liquid compositions are the synthetic anionic detergent compounds, and particularly a mixture of higher alkylbensene sulphonate and alkyl polyethoxy 5„ sulphate. While other water soluble higher alkyl-benzene sulphonates may also be present in the formulas of the present invention, such as potassium salts and in some instances the ammonium or alkanol-ammonium salts, where appropriate, it has been found 10. that the sodium salt is highly preferrede which is also the case with respect to the alkyl polyethoxy sulphate detergent component- The alkylbensene sulphonate is one wherein the higher alkyl group is of 12 to 15 carbon atoms, preferably 13 carbon 15. atoms- The alkyl polyethoxy sulphate, which also may be referred to as a sulphated polyethoxylated higher linear alcohol or the sulphated condensation product of a higher fatty alcohol and ethylene oxide or poly-ethoxylene glycolf is one wherein the alkyl group is 20. of 10 to 18 carbon atoms, preferably 12 to 15 carbon atoms, e.g. about 13 carbon atoms, and which includes 3 to 11 ethylene oxide groups, preferably 3 to 7, more preferably 3 to 5 and most preferably 3 or about 3 ethylene oxide groups. The ratio of alkylbensene 25. sulphonate to polyethoxy sulphate in the detergent mixture is preferably from about 2;1 to 6:1 and most preferably from about 2;1 to 4s1, by weight. At ratios above 5 s1f the physical stability of the product may be adversely affected. 30. In suitable circumstances other anionic deter- P12915 gents, such as fatty alcohol sulphates, paraffin sulphonates, olefin sulphonates, monoglyceride sulphates, sarcosinates and similarly functioning detergents, preferably as the alkali metal, e.g. 5. sodium salts, can be present, sometimes in partial replacement of the previously mentioned synthetic organic detergents but usually, if present, in addition to such detergents, formally, the supplementing detergents will be sulphated or 10„ sulphonated products (usually as the sodium salts) and will contain long chain (8 to 20 carbon atoms) linear or fatty alkyl groups. In addition to any supplementing anionic synthetic organic detergents, there also may be present nonionic and amphoteric 15. materials, like the Meodols (Registered Trade Mark)e sold by Shell Chemical Company,, which are condensation products of ethylene oxide and higher fatty alcohols, e.g. Maodol (Registered Trade Mark) 23-6.5, which is a condensation product of a higher fatty alcohol of 20. about 12 to 13 carbon atoms with about 6«5 moles of ethylene oxide„ Illustrations of the various detergents and classes of detergents mentioned may be found in the text Surface Active Agents, Vol. II, by Scwartz, Perry and Berch (Interscience Publishers, 25. 1958), the descriptions of which are incorporated herein by reference„ The builder salt combination of the present invention* which has bean found to satisfactorily improve the detergency of the mixture of synthetic 30„ anionic organic detergents and produce the desired pB P12915 . in the liquid detergent and in the wash water, is a mixture of sodium tripolyphosphate and sodium carbonate. The builder salts are employed in the compositions of the present invention in amounts 5„ generally of from about 5 to 25%, by weight. For the preferred builder salt combination, sodium tripolyphosphate is present in amounts of from about 5 to 20%, preferably 10 to 16%, and sodium carbonate is present from about 1 to 10%, by weight, preferably 3 10. to 7 %, the weight ratio of tripolyphosphate to carbonate in the preferred builder mixtures being from about 2;1 to 6:1, and most preferably from about 2si to 4:1. As used herein, the term alkali metal "carbonates" or "carbonate" is meant to include the 15, carbonates, bicarbonates and sesquicarbonates of such alkali metals.

For best processing, easier mixing and good end-use properties it is preferred that the sodium tripolyphosphate be low in content of Phase I type tri-20. polyphosphate. Thus, normally the content of Phase X type tripolyphosphate will be less than 30% of the tripolyphosphate employed.. Although in some instances incompletely neutralised tripolyphosphate may be used, normally the phosphate employed may be 25. considered as being pentasodium tripolyphosphate, Na5P30io- Of course, in some instances, as when potassium salts of other materials are presention interchange in an aqueous medium may result in other salts than the sodium tripolyphosphate being present 30„ but for the purpose of this specification it will be P12S15 11. considered that sodium tripolyphosphate» as the pentasodium salt, the material which is normally charged to the mixer to make the present liquid detergent, is the tripolyphosphate employed. 5. Other preferred builder salts which may be used in place of sodium tripolyphosphate and sodium carbonate or in addition thereto include a polyacetal carboxylase as herein described and sodium nitrilotriacetate (NTA)„ Of course, various mixtures 10, of the mentioned water soluble builder salts can be utilized- Yet, the tripolyphosphate-carbonate mixture described has been found to be most preferred, although the other builders and mixtures thereof are also operative. Other builders which may 15. be employed as supplements, in addition to the proportions of the above-mentioned builders, include other phosphates, such as tetrasodium pyrophosphate or tetrapotassium pyrophosphate, sodium bicarbonate, sodium citrate, sodium gluconate, sodium silicate, 20. and sodium sesquicarbonat®. Among the water insoluble builders •chat may be used are the zeolites, such as Zeolite h, usually in the for™, of its crystalline hydrate, although amorphous zeolites may also be useful.

. Polyacetal carboxylates are generally described in U.S. Patents 4„144,226 and 4,315,092. U.S. Patent 4,146,495 describes detergent compositions containing polyacetal carboxylates as builders.

The polyacetal carboxylates which are useful 30. herein as builders may be considered to be those P12915 12. described in U.S. Patent 4,144,226 and may be made by the method mentioned therein. A typical such product will be of the formula . a1 - (CHO)n - R2 COOM . . wherein M represents an alkali metal, or ammonium, or an alkyl group of 1 to 4 carbon atoms, or a tetra-alkylammonium group or an alkanolamine group, both of 1 to 4 carbon atoms in the alkyls thereof, n averages at least 4, and R^ and R- represent any chemically stable group which stabilises the polymer against rapid depolvmerization in alkaline solution. Preferably the polyacetal carboxylate will be one wherein M is alkali metals e.g. sodium, n is from 50 to 200, R1 is ch3ch2o hco- or , h3c or a mixture thereof, is ogh2ch3 mooc I h3c-co- I mooc -ch . ch3 and n averages from 20 to 100, more preferably 30 to P12915 13. 80. The calculated weight average molecular weights of the polymers will normally be within the range of 2,000 to 20,000, preferably 3,500 to 10,000 and more preferably 5,000 to 9,000, e.g. about 8,000. 5. A particularly preferred sodium polyacetal carboxylate is supplied by Monsanto Company and is known as Builder U» It has a calculated weight average molecular weight of about 8,000 and an active polymer content of about 80%.

. Although the preferred polyacetal carboxylates have been described above, it is to be understood that they may be wholly or partially replaced by other such polyacetal carboxylates or related organic builder salts described in the previously cited 15. patents on such compounds, processes tor the manufacture thereof and compositions in which they are employed. Also, the chain terminating groups described in the various patents, especially U.S., 4,144, 22S f may be utilised, providing that they have 20„ the desired stabilising properties, which allow the mentioned builders to be depolymerised in acidic media, facilitating bi©degradation thereof in waste streams, but maintain their stability in alkaline media, such as washing solutions. 25. The bentonite employed in the present invention is a colloidal clay (aluminium silicate) containing montmorillonite. Swelling bentonites are generally characterised as sodium bentonites, i.e. bentonite wherein the predominant cation is sodium. Among the 30. sodium bentonite clays, those from Wyoming (generally P12915 14. referred to as Western or Wyoming bentonite) are especially preferred.

The swelling capacity of bentonite is generally associated with its fabric softening properties. In 5» water the swelling capacity of sodium bentonite is in the range of 3 to 20 millilitres/gram, preferably 7 to 15 ml/gram, and its viscosity, at 6% concentration in water, is usually in the range of 3 to 30 centipoises, preferably 8 to 30 centipoisas. 10. Preferred swelling bentonites are sold under the trademark HI-JEL by Georgia Kaolin Co. These materials are the same as bentonites which were formerly sold under the trademarks MINERAL COLLOID and TB.IX0-JE.L,„ They are selectively mined and bene-15„ ficiated bentonites, and those considered to be most useful are available as HI-JEL Mos» 1, 2, 3 etc., corresponding to THIXO-JJSLs No's 1, 2, 3 and 4. Such materials have a maximum free moisture content (before addition to the liquid medium) of 4% to 8% 20. and specific gravities of about 2.6. The bentonite is preferably one which will pass through a 200 mesh U.S. Sieve Series sieve, and most preferably at least 90% of the particles will pass through a Mo. 325 sieve, so that the equivalent diameter of the 25. bentonite may be considered to be less than 74 microns, and more preferably less than about 44 microns.

Typical chemical analyses of some bentonites that are useful for making the liquid detergents of 30. the present invention show that they contain from P12SI5 . 64.8 to 7 3.0% of Si(>2, 14 to 18% of A1203, 1.6 to 2„7% of MgO, 1.3 to 3.1% of CaO, 2.3 to 3-4% of Fe2C>3, 0.8 to 2,8% of Ne^O and 0.4 to 7.0% of ^O.

Although the western bentonites are preferred it 5o is also possible to utilise other bentonites, such as those which may be made by treating Italian or similar bentonites containing relatively small proportions of exchangeable monovalent metals (sodium and potassium) with alkaline materials, such as 10. sodium carbonate, to increase the cation exchange capacities of such products. It is considered that the Ma20 content of the bentonite should be at least about 0.5%, preferably at least 1% and more preferably at least 2% so that the clay will be 15o satisfactorily swelling, with good softening and dispersing properties in aqueous suspension.

Preferred swelling bentonites of the types described above are sold under the trade names Laviosa and Winkelmann, e.g. Laviosa AGs and Winkelmann G-13„ 20 Other bentonites which are particulars useful for the present liquid detergent compositions because of their white or very light colour include American Colloid Company's Polarite KB 325t. a California bentonite^ and Georgia Kaolin1s GK 129, a Mexican 25. bentonite™ The only other required component of the liquid detergents of the present invention is water.

Normally the hardness content of such water will be less than about 300 ppmP as CaCOg, and preferably it 30 will be less than 150 ppm. Often it may be desirable P12915 16. to utilise deionised water although city water with less than 50 or 100 p.p.m. hardness content will frequently be equally satisfactory.

Various adjuvants may be present in the liquid 5. detergents of the present invention, such as fluorescent brighteners, perfumes and colourants . The fluorescent brightaners include the well known stilbene derivatives, including the cotton and nylon brighteners, such as those sold under the trademark 10. Tinopal (5BM Cone.). The perfumes that are employed usually include essential oils, esters, aldehydes and/or alcohols, all of which are known in the perfumery art. The colourants may include dyes and water dispersible pigments of various types, 15. including ultramarine blue. Inorganic filler salts, such as sodium sulphate and sodium chloride may be present , as may be antiredeposition agents, such as sodium carboxymethylcellulose; dispersing agents, such as sodium polyacrylate; bleaches; bactericides; 20. fungicides; anti-foam agents, such as silicones; anti-soiling agents, such as copolyesters; preservatives such as formalin; foam stabilizers, such as lauric myristic diethanolamide; and auxiliary solvents, such as ethanol. Normally the individual proportions of 25. such adjuvants will be less than 3%, often less than 1% and sometimes even less than 0.5%, except for any fillers and solvents, and additional detergents and builders for which the proportions may sometimes be as high as 10%. The total proportion of adjuvants, 30. including non-designated synthetic detergents and builders, will normally be no more than 20% of the P12915 17. product and desirably will be less than 10% thereof, more desirably less than 5% thereof. Of course, the adjuvants employed will be selected so as not to interfere with the washing action of the liquid 5„ detergent and to avoid instability of the product on standing. Also, adjuvants which cause the production of objectionable deposits on the laundry are to be avoided.

The liquid compositions of the present invention 10„ are efficient and easy to use. Compared to heavy duty laundry detergent powders, much smaller volumes of the liquids of the present invention are employed to obtain comparable cleaning of soiled laundry. For example, using a typical preferred formulation of the 15. present invention, only about 132 grams or 1/2 cup of liquid is needed for a full tub of wash in a top-loading washing machine in which the aatar volume is 15 to 18 gallons (57 to 68 litres); and even less is needed for front-loading machines. Thus, the 20. concentration of the liquid detergent composition in the wash water is of the order of about 0„2%„ Usually, the amount 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 25. the various constituents of the liquid composition may vary accordingly. Equivalent results can be obtained by using greater amounts of a more dilute formulation but the greater quantity needed will require additional packaging and will generally be 30less convenient for consumer use and may also result in product separation.

P12915 18.

The viscosity of the liquid detergent composition of the present invention, is normally in the range of about 1000 to 10,000 centipoises, preferably 2000-5000 centipoises, but products of other suitable viscosi-5- ties may also be useful. At the viscosities mentioned, the liquid detergent is pourable, stable, non-separating and uniform. The pH of the liquid detergent suspension usually in the range of 7 to 11.5, preferably 8 to 10.5, appears to help to 10. maintain product stability and pourability.

The invention may be put into practice in various ways and a number of specific embodiments will be described to illustrate the invention with reference to the accompanying examples. Unless 15. otherwise indicated all parts are by weight and temperatures are in °C„ EXAMPLE 1 A liquid detergent composition is made up with the ingredients and proportions shown in Table 1 . below.

TABLE 1 Component Percent Pentasodium tripolyphosphate 11.0 Bentonite (Georgia-Kaolin 129) 12.0 . Sodium carbonate 2.0 Sodium sesquicarbonate 2.0 Sodium linear tridecvlbensene sulphonate 8.0 AEOS(1) 3.0 Carboxymethyl cellulose (CMC) 0.2 . Optical brightener 0.3 Perfume 0.4 Ensyme (Esperase 8.0L)(^) P12S15 19.

Component TABLE 1 (continued) Glycerine Borax Citric Acid Water and adjuvants Percent 3.0 2.5 2.0 Balance Notes on Table 1; Sodium alkyl polyethoxy sulphate aha rein the 10. alkyl group is of 12 to 15 carbon atoms and the polyethoxy is of 3 ethoxv groups. (2) "Esperase" sold by Movo Industries having an activity of 8.0 KMPU/gram (Kilo Movo Protease 15. units/gm).

The composition set out in Table 1 Mas prepared by the following procedures 30.0 parts of deionised Mater at 40°F (4°C) are added to a suitable mixing 20. apparatus such as a vertical cylindrical tank equipped with a stirrer. With the stirrer adjusted for medium agitation, a mixture consisting of 2 0 parts anhydrous soda ash« 2,0 parts sodium sesquicarbonate , and 0.2 parts sodium carboxymethyl 25. cellulose is incorporated into the water. The stirrer speed is then increased to maximum agitation and a mixture comprised of 11.0 parts pentasodiusn tripolyphosphate and 12.0 parts bentonite is slowly added to the mixing apparatus over a period of 10-15 30. minutes to form an off-«hite suspension. The P12915 . agitation speed is then decreased to a slow/medium setting while 8.64 parts of a high AI (about 55%) LTBS (linear tridecylbensene sulphonate) slurry is added. Thereafter the optical brightener/ colour solution is added consisting of 0.3 parts Tinopal LMS-X (CIBA-GEXGY), 0.9S parts colourant, and 4.02 parts deionised water. Once a uniform blueish-green coloured solution is obtained, 0.4 parts of perfume are added to the mixture under agitation. This is followed by the slow addition of 3.0 parts glycerine and 2.5 parts borax as a two component slurry,, Stirring is continued until the mixture is uniform in appearance and then 2.0 parts of sodium citrate and 9.0 parts water are slowly added. Agitation of the mixture is then reduced while 10.95 parts of a mixed AI detergent base consisting of an LTBS slurry (about 30% AI) and AEOS (about 27.5% AI) is added to the mixture. This is followed by the slow addition of 1.0 part proteolytic ensyme with continuous agitation until all materials are completely dispersed or dissolved.

EXAMPLES 2A to 2G Enzyme-containing built liquid detergent compositions, Examples 2A to 2G, were formulated as set forth below in Table 2. The percentages shown indicate weight percent. It will be appreciated that the compositions are identical in respect of the first ten components listed in Table 2.

Examples 2A to 2F are comparison examples.

P12915 . , . , 21. 1 TABLE 2 Component 2A 2B 2C 2D 2E 2F 2G Pentasodium tri 11.0 11.0 11.0 11.0 11.0 11.0 11 J polyphosphate Bentonite 12.0 12 .0 12.0 12.0 12.0 12.0 12.

(Georgia-Kaolin 129) Sodium Carbonate 2.0 2.0 2.0 2.0 2.0 2.0 2.0 Sodium sesquicar- 2 . 0 2 „0 2.0 2.0 2.0 2.0 2.0 bonate Sodium linear tri- 8,0 8.0 8.0 8.0 8.0 8.0 8.0 decylbenzene sulphonate AEOsU) 3 -0 3.0 3.0 3.0 3.0 3.0 3.0 Optical brightener 0.3 0.3 0.3 0.3 0.3 0.3 0.3 (Tinopal LMS-X) Perfume 0.4 0 „4 0.4 0.4 0.4 0.4 0.4 CMC 0.2 0 „ 2 0.2 0.2 0.2 0.2 0.2 Ensyme(2) 1.0 1.0 1.0 1.0 1.0 1.0 1.0 Glycerine - 3.0 - 3.0 - - 3.0 Borax - - 2.5 2.5 - 2.5 2.5 Carboxylic acid - - - - 2.0 2.0 2.0 , compound Water and adjuvants Balance , Motes on Table 2; (1) Sodium alkyl polyethoxy sulphate wherein the alkyl group is of 12 to 15 carbon atoms and the polyethoxy is 3 of ethoxy groups™ (2) "Esperase" sold by Novo Industries having an activity of 8„0 KMPU/gsa (Kilo Movo Protease units/gm).

P12915 22.

The ensyme activities of the compositions of Examples 2A to 2G were tested after 7 days storage at 110°F (43°C) . The measured ensyme activity for each composition after this period of storage is indicated 5» in Tables 3A to 3C and Table 4 as a percent of the initial value. The various carboxylic acids and salts used in the formulas of the compositions of Examples 2A to 2D are shown in Table 3A as well as the enzyme activities corresponding to each composi-10. tion; for Example 2E in Table 3B (these all being comparison examples) and for Example 3G in Table 3C (this being in accordance with the invention).

TABLE 3A ENZYME STABILITY . Percent Active Ensyme After 7 Days at 110°F Example Composition (43°C) 2A (control) ND* 2B (with glycerine) MD 2C (with borax) HD 2D (with glycerine and borax) 45 .

P12915 23.

TABLE 3B Composition E (with carboxylic acid compound) wherein the carboxylic acid compound is; Percent Active Ensyme After 7 Days at 110°F Example Composition (43°C) 2E (1) Succinic acid MD* 2E (2) Malonic acid MD 2E (3) Malic acid MD 2E (4) Tartaric acid LMD 2E (5) Aspartic acid MD 2E (6) Citric acid MD 2S (7) Sodium tartrate MD 2E (3) Sodium citrate MD Mote on Tables 3A and 3B * MD ~ Mot detectable (below % residual activity)- TABLE 3C Composition G (with glvcerir?,e/borax/carboxylic 20. acid compound) wherein the carboxylic acid compound is; Percent Active Ensyme Aftar 7 Days at 110°F Example Composition (43 °C) « 2G (1) Succinic acid 70 2G (2) Malonic acid 70 2G (3) Malic acid 78 2G (4) Tartaric acid 73 2G (5) Aspartic acid 90 - 2G (6) Citric acid 74 2G (7) Sodium tartrate 66 2G (8) Sodium citrate 52 P12915 24.

As is evident from Table 3A, the control composi tion of Example 2A, as well as the comparison composi tions of Examples 23 and 2C which contained glycerine and borax, respectively, as individual stabilizers* 5. manifested almost no enzyme activity after the 7 day storage period of 110°F (43°C). Since enzyme activities below 10% could not be precisely measured they are designated "MD". The comparison composition of Example 2D containing glycerine and borax in the 10. absence of a carboxylic acid compound provided an improvement in enzyme stability relative to the compositions of Examples 2A to 2C but about 50% of the enzyme was deactivated™ The various comparison compositions of Examples 2E(1) to 2E(8) containing a 15. variety of carboxylic acid compounds but no borax or glycerine, as indicated, manifested absolutely no improvement in enzyme stability relative to the compositions of Examples 2A to 2C. However, the compositions of Examples 2G(1) to 2G(8) formulated in 20. accordance with the invention (using the same carboxylic acids) demonstrate the unexpected and synergistic improvement in enzyme stability which is achieved with the use of glycerine and borax in combination with a carboxylic acid compound in liquid 25. detergent compositions as required by the present invention™ It is noted that almost every one of the compositions corresponding to Examples 2G(1) to 2G(8) demonstrated a significant improvement in enzyme activity relative to the composition of Example 2D 30. (containing only glycerine and borax)™ P12915 .

A comparison of the enzyme activities achieved with the composition of Example 2D (glycerine and borax) and various compositions of Example 2F (borax and carboxylic acid compound) and of Example 2G 5. (formulated in accordance with the invention) is set forth below in Table 4„ TABLE 4 ENZYME STABILITY . Percent Active Enzyme After 7 Days at 110°F Example Composition (43 °C) 2D (Glycerine/borax) 59 2F (1) (Sorax/malonic acid) 45 2G (2) (Glycerine/borax/malonic acid) 70 2F (2) (Borax/aspartic acid) 72 2G (5) (Glycerine/bore^/aspartic acid) 90 2F (3) (Borax/citric acid) 42 2G (6) (Glycerine/borax/citric acid) 74 , .

. Motes on Table 4 2F(1) corresponds to 2G(2); 2F(2) corresponds to 2G(5) and 2F(3) corresponds to 2G(6)„ As shown in Table 4, the various compositions of Example 2G(2), 2G(5) and 2G(6) containing a three component stabilizer system in accordance with the present invention provided a synergistic improvement in ensyme stability relative to the compositions of 30„ Examples 2D and 2F(1), 2F(2) and 2F(3) formulated in accordance with the prior art.

Claims (14)

claims

1. „ A stabilized fabric sofhening enzyme-containing built liquid detergent composition comprising; (a) from 5 to 20%, by weighh, of one or more surface active detergent compounds selected from the group consisting of anionic,, nonionic and amphoteric detergent compounds; (b) from 5 to 30%t by weight,, of one or more builder salts selected from the group consisting of alkali metal tripolyphosphates,, alkali metal carbonates, alkali metal nitrilotriacetates and polyacetal carbossylates; (c) from 5 to 20%, by weight,, of a swelling bentonite clay; (d) an effective amount of an ensyme or an enzyme mixture selected from the group consisting of alkaline protease enzymes and alpha-amylase enzymes; (e) an enzyme-stabilizing system containing,, based on the weight of the detergent composition, (i) from 1% to 10% glycerine; (ii) from 1 to 8% of a boron compound selected from the group consisting of boric acid, boric oxide and alkali metal borates,- and (iii) from 0.5 to 8% of a carboxylic acid compound selected from the group consisting of mono, di and polycarboxylie acids having 1 to 8 carbon atoms and water-soluble salts thereof; and (f) the balance comprising water and optionally perfume and other adjuvants. 27.

2. A liquid detergent composition as claimed in Claim 1 comprising: (a) from 5 bo 15% of an alkali metal alkyl-benzene sulphonate in which the alkyl group contains 12 bo 15 carbon atoms; (b) from 2 bo 5% of an alkali mebal alkyl polyethoxy sulphate in which the alkyl group contains 10 bo 18 carbon atoms and the polyethoxy is of 3 to 11 ethylene oxide groups, bhe weight ratio of (a) bo (b) being from about 2:1 to about 8:1; (c) from 5 to 20% of sodium tripolyphosphate ; (d) from 1 to 10% of sodium carbonate, the weight ratio of (c) to (d) being from 2:1 bo 6:1; (e) from 10 to 15% of a sodium bentonite; (f) an effective amounb of bhe said ensyme or ensyme mixture? (g) the ensyme stabilizing system containingt. based on the weight of bhe detergent composition? (i) from 3 bo 7% glycerinef (ii) from 1 bo 5% of an alkali metal borabe and (iii) from 0.5 to 4% of bhe said carboxylic acid compound; and (h) the balance comprising water and optionally perfume and other adjuvants.

3. A liquid detergent composition as claimed in Claim 2 in which bhe said alkali metal alkylbenzene sulphonate is sodium linear tridecyl-benzene sulphonabe and the said alkali metal alkyl 28. polyethoxy sulphate is one in which the alkali metal is sodiunip the alkyl group contains 12 to 15 carbon atoms and the polyethoxy is of about 3 ethylene oiside' groups.

4. A liquid detergent composition as claimed in Claim 2 or Claim 3 in which the ratio of alkylbensene sulphonate to polyethoxy sulphate is from 2:1 to 4:1.

5. A liquid detergent composition as claimed in any one of Claims 1 to 4 in which the said boron compound is an alkali metal borate.

6. S„ A liquid detergent composition as claimed in Claim 5 in which the said borate is borax.

7. , A liquid detergent composition as claimed in any one of Claims 2 to 5 which contains from 8 to 16% sodium tripolyphosphate and from 2 to 6% sodium carbonate or sodium bicarbonate or mixtures thereof.

8. , A liquid detergent composition as claimed in any one of Claims 1 to 7 in which the said carboxylic acid compound is aspartic acid or a water-soluble salt thereof.

9. , A liquid detergent composition as claimed in any one of Claims 1 to 7 in which the said carboxylic acid compound is tartaric acid or a water-soluble salt thereof. 29.

10. A liquid detergent composition as claimed in any one of Claims 1 to 7 in which the said carboxylic acid compound is citric acid or a water-soluble salt thereof,

11. A liquid detergent composition as claimed in any one of Claims 1 to 7 in which the said carboxylic acid compound is malonic acid or a water-soluble salt thereof.

12. A liquid detergent composition as claimed in any one of Claims 1 to 7 in which the said carboxylic acid compound is malic acid or a water-soluble salt thereof,

13. A liquid detergent composition as claimed in Claim 1 substantially as specifically described herein with reference to any one of Example 1 or Examples 2G(1) to 2G(8).

14. A method of laundering comprising contacting the stained and/or soiled fabrics to be laundered with a stabilized enzyme-containing built liquid detergent composition as claimed in any one Claims 1 to 13. TOMKINS & CO.