GB1577120A - Liquid detergent compositions - Google Patents

Liquid detergent compositions Download PDF

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Publication number
GB1577120A
GB1577120A GB21428/76A GB2142876A GB1577120A GB 1577120 A GB1577120 A GB 1577120A GB 21428/76 A GB21428/76 A GB 21428/76A GB 2142876 A GB2142876 A GB 2142876A GB 1577120 A GB1577120 A GB 1577120A
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Prior art keywords
sodium
weight
compositions
sodium tripolyphosphate
copolymer
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GB21428/76A
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Unilever PLC
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Unilever PLC
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Application filed by Unilever PLC filed Critical Unilever PLC
Priority to GB21428/76A priority Critical patent/GB1577120A/en
Priority to GR53505A priority patent/GR63137B/en
Priority to FI771609A priority patent/FI771609A/fi
Priority to DE2722988A priority patent/DE2722988C2/en
Priority to AT0367377A priority patent/AT362851B/en
Priority to FR7715791A priority patent/FR2352878A1/en
Priority to BR7703301A priority patent/BR7703301A/en
Priority to SE7706014A priority patent/SE433087B/en
Priority to CH634277A priority patent/CH628370A5/en
Priority to JP5969777A priority patent/JPS52146407A/en
Priority to DK225777A priority patent/DK148100C/en
Priority to BE177798A priority patent/BE854906A/en
Priority to ZA00773065A priority patent/ZA773065B/en
Priority to NO771785A priority patent/NO771785L/en
Priority to IT7768176A priority patent/IT1083001B/en
Priority to NL7705673A priority patent/NL7705673A/en
Priority to LU77404A priority patent/LU77404A1/xx
Priority to CA278,973A priority patent/CA1100382A/en
Priority to PT66595A priority patent/PT66595B/en
Priority to ES459099A priority patent/ES459099A1/en
Publication of GB1577120A publication Critical patent/GB1577120A/en
Expired legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3765(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in liquid compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

The aqueous, heterogeneous, stable, liquid detergent contains a) 2 to 20 per cent by weight of a detergent material from the group of non-soap-like, anionic, non-ionic, amphoteric, zwitterionic, synthetic surfactants, soaps of C10-C22 fatty acids, soaps of dimerised C10-C22 fatty acids and their mixtures, b) at least 2 per cent by weight of sodium tripolyphosphate, c) at least 2 per cent by weight of sodium or potassium orthophosphate, where the total of ingredients b) and c) is 5 to 35 per cent by weight, and the b) : c) ratio is 10 : 1 to 1 : 10 by weight, and d) 0.1 to 2 per cent by weight of a copolymer of maleic anhydride with ethylene, styrene or vinyl methyl ether in an aqueous medium.)

Description

(54) LIQUID DETERGENT COMPOSITIONS (71) We, UNILEVER LIMITED, a company organised under the laws of Great Britain, of Unilever House, Blackfriars, London E/C 4, England, do hereby declare the invention for which we pray that a patent may be granted to us and the method by which it is to be performed, to be particularly described in and by the following statement:- The invention relates to liquid detergent compositions which are suitable for fabric washing, and in particular to such compositions containing phosphate detergency builders.
Aqueous built liquid detergent compositions are well known in the art. Although they offer several advantages over other forms of detergent compositions like powders, such as improved solubility and easier dosing, their formulation is very difficult, since they should be physically stable under a wide range of storage conditions, for example from about --4"C to +37"C.
Also they should have satisfactory pouring properties despite containing relatively high concentrations of detergent ingredients, especially builder salts so that ideally they have performances equivalent to the usual powdered detergent compositions.
The prior art mainly teaches the use of more water soluble ingredients, such as tetrapotassium pyrophosphate, usually with expensive stabilising agents, but even then the amount which can be used is lower than would be desired in comparison with powdered detergent compositions. Although such prior liquid formulations may provide acceptable compositions as far as their physical characteristics are concerned, their detergency and other washing properties tend to be unsatisfactory. For example, with the alkali metal pyrophosphates there are often deposits formed on the clothes, especially when the products are used at exceptionally low product concentrations or at high temperatures. When attempts have been made to improve the detergency, then the stability and pourability have become unsatisfactory.In particular, it has not been possible to incorporate into the liquid detergent compositions sufficiently high levels of the conventional detergency builders such as sodium tripolyphosphate without causing severe problems of separation or solidification of the liquid compositions.
According to the present invention we have found that satisfactory, relatively high, levels of certain mixtures of sodium tripolyphosphate and sodium of potassium orthophosphate may be incorporated into aqueous heterogeneous stable liquid compositions, that is compositions with a suspended solid phase, which have good physical properties, with the aid of particular stabilising agents as described hereinafter.
Instead of the sodium tripolyphosphate the potassium salt may be used, but this is more expensive and for convenience the use of the sodium salt is described and illustrated in the specification.
Insofar as these two detergency builder materials function normally in different ways i.e. by sodium tripolyphosphate acting as a sequestrant detergency builder and the alkali metal orthophosphate functioning as a precipitant builder, it is somewhat surprising that a mixture of the materials functions so effectively. In particular, when sodium orthophosphate is used alone as a detergency builder it tends to cause inorganic deposition on the washed fabrics, which is accompanied by soil redeposition, but in the presence of the sodium tripolyphosphate the soil redeposition is significantly decreased whilst the detergency is appalently boosted.Moreover, in comparison with the use of sodium tripolyphosphate alone as detergency builder, the same amount of the mixed sodium tripolyphosphate and alkali metal orthophosphate detergency builders shows improved detergency and soil redeposition properties, especially in hard water.
There have in the past been many suggestions for using mixed phosphate detergency builders, for example mixtures of sodium pyrophosphate and sodium tripolyphosphate, in liquid compositions, particularly those adapted for hard surface cleaning.
Moreover, it is well known that the condensed phosphates such as sodium tripolyphosphate tend to degrade in aqueous alkaline conditions at high temperatures.
which are often met during detergent processing conditions, so as to form other phosphates; for example sodium tripolyphosphate tends to break down to give a mixture of sodium pyrophosphate and sodium orthophosphate.
However, to the Applicants' knowledge it hts not been proposed hitherto to use the specific mixtures of sodium tripolyphosphate and alkali metal orthophosphate in the proportions as set out below in fabric washing liquid detergent compositions containing a suspended solid phase according to the present invention. The formation of the heterogeneous detergent compositions with much higher detergency builder levels than has hitherto been possible is particularly advantageous. They can be made with good physical properties without very expensive multiple stabilising agent systems or complicated processing conditions.
The ratio of the sodium tripolyphosphate to the alkali metal orthophosphate in the detergent composition is from 10:1 to 1:10, particularly 5:1 to 1:2 parts by weight.
preferably from 4:1 to 2:3, and especially from 3:1 to 1:1 parts by weight. These ratios of sodium tripolyphosphate to the alkali metal orthophosphate are chosen to give optimum detergency building and other washing properties in relation to the maximum amount of these ingredients which can be tolerated in the liquid compositions without loss of stability.
It will be appreciated that the actual amounts of sodium tripolyphosphate and alkali metal orthophosphate are chosen according to the overall phosphate detergency builder level which is desired or permitted in the liquid detergent compositions.
However, it is normal to use a total amount of sodium tripolyphosphate plus alkali metal orthophosphate within the range of from 5% to 35% by weight of the composition, preferably from 10% to 30%, especially 15% to 25% by weight. It is also preferred that the individual amount of each of the sodium tripolyphosphate and the alkali metal orthophosphate should be at least 2%, preferably at least 4% by weight of the composition.
When higher levels of sodium tripolyphosphate are used, i.e. above 12% by weight of the composition, it is particularly advantageous to use a type of sodium tripolyphosphate which hydrates rapidly, as this aids its solubility, particularly for use in compositions containing higher levels of sodium tripolyphosphate. Suitable materials are commercally available with a high, i.e.
greater than 50%, phase I content, and they may also be partially or fully prehydrated.
Apart from the mixed phosphate detergency builders, the liquid detergent compositions of the invention contain a detergent active compound which may be an anionic, nonionic, amphoteric or zwitterionic detergent active compound or mixture thereof. Many suitable detergent active compounds are commercially available and are fully described in the literature, for example in "Surface Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
The preferred detergent compounds which can be used are synthetic anionic compounds. These are usually water soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from 8 to 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.Examples of suitable synthetic anionic detergent compounds are sodium and potassium primary or secondary alkyl sulphates, especially those obtained by sulphating the higher (C8-CI8) alcohols produced by reducing the glycerides of tallow or coconut oil: sodium and potassium alkyl (C-G benzene sulphonates, particularly sodium linear secondary alkyl (C1-C15) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty acid monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C,-Cls) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acids amides of methyl taurine; primary or secondary alkane monosulphonates such as those derived by reacting alphaolefins (Cs-Gn) with sodium bisulphite and those derived by reacting paraffins with SO2 and Cl and then hydrolysing with a base to produce a random sulphonate; and olefin sulphonates, which term is used to describe the material made by reacting olefins, particularly alpha-olefins, with SO3 and then neutralising and hydrolysing the reaction product.
Although in general the sodium salts of the anionic detergent compounds are preferred for cheapness, the potassium salts can sometimes be used to advantage, particularly in compositions with high levels of other sodium salts such as sodium tripolyphosphate and sodium orthophosphate.
Of the anionic detergent compounds, alkali metal alkyl (C10-C15) benzene sulphates are particularly preferred, both for ready availability and cheapness and also for their advantageous solubility properties.
If desired, nonionic detergent active compounds may be used as the sole detergent compounds, or preferably in admixture with anionic detergent compounds, especially the alkyl benzene sulphonates. Examples include the reaction products of alkylene oxides, usually ethylene oxide, with alkyl (C6-C,) phenols, generally 5 to 25 EO; i.e.
5 to 25 units of ethylene oxide per molecule; the condensation products of aliphatic (C8-C18) primary or secondary alcohols with ethylene oxide, generally 2 to 30 EO, e.g.
6-20 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Another example of suitable nonionics are nonionics obtained by first ethoxylating and subsequently propoxylating an organic hydroxyl-group containing radical, e.g. an aliphatic primary or secondary Cs-Cis alcohol. Other so-called nonionic detergent active compounds include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
Mixtures of detergent active compounds, for example mixed anionic or mixed anionic and nonionic compounds may be used in the detergent compositions, particularly to impart thereto controlled low sudsing properties. This is particularly beneficial for compositions intended for use in suds-intolerant automatic washing machines. Mixtures of amine oxides and ethoxylated anionic compounds can also be beneficial.
Amounts of amphoteric or zwitterionic detergent active compounds can also be used in the liquid detergent compositions of the invention but this is not normally desired due to their relatively high cost. If any amphoteric or zwitterionic detergent active compounds are used it is generally in small amounts in compositions based on the much more commonly used anionic and/or nonionic detergent active compounds. Soaps, i.e. alkali metal salts such as sodium or potassium salts of Clo-C, fatty acids such as coconut fatty acids and oleic acid, including polymeric fatty acids such as dimerized oleic acid, may also be used in the compositions of the invention, particularly in ternary mixtures with synthetic anionic and nonionic detergent active compounds, which have low sudsing properties.
The amount of the detergent active compound or compounds used is generally in the range of from 2.0% to 20%, preferably 5% to 15%, by weight of the compositions, depending on the desired properties. Lower levels of nonionic detergent compounds should be used within this range as they tend to form a separate liquid phase if used at higher levels, that is over 5% by weight.
The ratio of the total detergent active compounds to the total of the amount of sodium tripolyphosphate and alkali metal orthophosphate should generally be in the range of from 2:1 to 1:5, preferably 1:1 to 1:3 parts by weight.
The alkali metal orthophosphate used may be sodium or potassium orthophosphate. The former is cheaper and more readily available but the latter may be advantageously used, particularly at high total phosphate levels in the products. The potassium orthophosphate can be added as such, or orthophosphoric acid may be neutralised by a potassium salt such as potassium hydroxide during production of the compositions. It should be noted that the term alkali metal orthophosphate includes the mono-, di- and tri-orthophosphates.
In the liquid detergent compositions of the invention it is essential to have present a stabilising agent, particularly in compositions containing higher phosphate levels, to maintain stable suspensions of the solid phase and/or to avoid separation of different liquid phases, particularly when nonionic detergent compounds are present.
Suitable stabilising agents for these compositions are polymeric stabilising agents which are copolymers of maleic anhydride with either ethylene, styrene or preferably vinyl methyl ether. Such materials are commercially available, for example under the trade name "Gantrez", for 1:1 copolymers of maleic anhydride with vinyl methyl ether, which have a specific viscosity of 0.1 to 4.5, preferably 0.1 to 0.6 (measured in solution (1 g in 100 ml) of methyl ether ketone at 25"C). Other copolymers of maleic anhydride with ethylene are available under the trade name "EMA". The copolymers are hydrolysed and neutralised in the compositions and they may also be partially esterified with any nonionic compound used.It should be noted that the presence of hydrotropes may be undesirable in the compositions, particularly at higher levels where they may detract from the stability of the products.
The amount of such copolymeric stabilising agents is preferably 0.1% to 2%, especially 0.3% to 1.5%, by weight of the composition.
It is desirable to include one or more anti-deposition agents in the liquid detergent compositions of the invention, to decrease any tendency to form inorganic deposits on washed fabrics, especially under conditions of use at low product concentration. Examples of preferred anti-deposition agents are homo- and copolyacrylates, e.g. sodium polyacrylate, the sodium salt of copolymethacrylamidelacrylic acid and sodium poly-alpha-hydroxyacrylate, and the sodium salts of polymaleic acid and polyitaconic acid. Such copolymers preferably have relatively low molecular weights, e.g.
in the range of 2,000 to 50,000. Other anti-deposition agents include phosphate esters of ethoxylated aliphatic alcohols, polyethylene glycol phosphate esters, and certain phosphonates such as sodium ethane- 1 -hydroxy- 1,1 -diphosphonate, ethylenediamine tetramethylene phosphonic acid and sodium 2-phosphonobutane tricarboxylate. The most preferred anti-deposition agent is sodium polyacrylate having a MW of 2,000 to 30,000, e.g. 15 to 25,000. The amount of such anti-deposition agents is generally 0.1% to 5.0%, preferably 0.2% to 2% by weight of the compositions.
It is also possible to include in the detergent compositions of the invention minor amounts, for example up to 10% by weight, of other detergency builders, which may be either so-called precipitant builders or sequestrant builders. This may be of particular benefit where it is desired to increase detergency whilst using particularly low levels of the essential sodium tripolyphosphate and alkali metal orthophosphate builders, so as to achieve particularly low phosphorus contents in the detergent compositions for environmental reasons.
Examples of such other detergency builders are amine carboxylates, such as sodium nitrilotriacetate. However, it is desirable to have no other phosphate detergency builders present other than the sodium tripolyphosphate and alkali metal orthophosphate, and in particular it is desirable to exclude pyrophosphates from the compositions as they tend to increase inorganic deposition and soil redeposition. Some pyrophosphate may be present for example as an impurity in the sodium tripolyphosphate, or it may be produced by hydrolysis of the sodium tripolyphosphate during detergent processing, particularly under alkaline conditions at elevated temperatures, so low levels of sodium pyrophosphate may be unavoidable, but it is preferred to have no more than 5%, especially less than 2% by weight of pyrophosphate present in the compositions.
The liquid detergent compositions of the invention can contain any of the conventional additives in the amounts in which such additivies are normally employed in liquid fabric washing detergent compositions. Examples of these additives include lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids, lather depressants such as alkyl phosphates, silicones and long chain soaps, anti-redeposition agents such as sodium carboxymethylcellulose, alkaline salts such as sodium silicate, alkali metal carbonate or alkali metal hydroxides, fabric softening agents, and, usually present in very minor amounts, fluorescent agents, perfumes, enzymes such as proteases and amylases, germicides and colourants.
The balance of the compositions is water, which is usually present to the extent of 40% to 75% by weight, preferably 45% to 65% by weight.
To ensure effective detergency the liquid detergent compositions should be alkaline, and it is preferred that they should provide a pH within the range of 9 to 12, preferably pH 9.5 to 11 when used in aqueous solution of the composition at the recommended concentration. To meet this requirement, the undiluted liquid composition should also be of high pH, for example pH 11 to 12.5. It should be noted that an excessively high pH, e.g. over pH 13 is less desirable for domestic safety. The ingredients in any such highly alkaline detergent composition should of course be chosen for alkaline stability, especially for pH-sensitive materials such as enzymes, and a particularly suitable proteolytic enzyme in this respect is available under the trade name "Esperase".
It is desirable to include in the composition an alkaline buffer, for example alkali metal carbonate, to maintain the pH of at least 9 during use, particularly under conditions of use, for example in hard water or at low product concentrations, when the alkali metal orthophosphate is precipitated in the form of its calcium salt and cannot itself then act as the alkaline buffer. Alternatively, alkali metal silicates, for example sodium ortho-, meta- or preferably neutral or alkaline silicates may be used. The presence of such alkali metal silicates at low levels of, for example 1% to 5% by weight, is also advantageous in decreasing the corrosion of metal parts in washing machines. An alkali metal hydroxide may alternatively or additionally be used to provide an initially high pH.
The liquid detergent compositions can be made relatively easily. It is preferable, particularly for products with lower sodium tripolyphosphate levels, to split the water required into two parts and one part is heated and then mixed with the inorganic builder salts and the other is mixed with the other organic ingredients. The two parts are then blended together to give a suspended liquid system. Alternatively, compositions of higher sodium tripolyphosphate content in particular may be made by firstly dissolving a preformed copolymeric stabilising agent in water and partly esterifying the copolymer with some nonionic detergent active compound, adding the anionic detergent active compounds, any soap and any further nonionic compound to the resultant mixture, and then adding the phosphate salts and any sodium silicate.The heat of reaction between acidic and alkaline ingredients may be used to raise the temperature and facilitate mixing of the ingredients. The resultant compositions have viscosities in the range from 50 to 2,000 centipoise, especially 100 to 1500 centipoise, as measured at room temperature in a Brookfield viscometer (Spindle No. 3, 30 rpm).
The invention is illustrated by the following Examples in which parts and percentages are by weight except where otherwise indicated.
Example I and 2 Two stable heterogeneous liquid compositions were made to the following formulations: Ingredient Percentages Ex I Ex 2 Sodium alkyl (C3-,) benzene sulphonate 6 6 Tallow alcohol - 18 EO 2 2 Alkyl phosphate 1 1 Dimerised oleic acid 2 2 Coconut ethanolamide - - Sodium tripolyphosphate 10 10 Sodium orthophosphate 8 8 Stabilising agent 3 1 1 Water . 72 71 1 Obtained as Hostaphat Obtained as Empol, neutralised to the sodium salt in processing 1 Copolymer of maleic anhydride with vinyl methyl ether 1::1, obtained as Gantrez AN 119, hydrolysed and neut rallised in processing The composition of Examples 1 and 2 had low sudsing properties due to the alkyl phosphate or the dimerised fatty acid, and were suitable for use in front loading automatic washing machines. In these examples, the combined amount of sodium tripolyphosphate and sodium orthophosphate were equivalent in hard water detergency building properties to a level of about 35% of sodium tripolyphosphate alone, which of course is more than could be included into a stable aqueous liquid detergent composition.
Examples 3 to 5 Three stable, heterogeneous built liquid detergent compositions were prepared to the following formulations: Ingredient Percentages Vex 3 Ex4 Ex5 Alkanol (C31 -C15) - 11 EO 2.5 2.5 2.5 Potassium alkylbenzene 1 sulphonate 6.5 6.5 6.5 Sodium tripolyphosphate 11.0 16.0 18.0 Potassium tripolyphosphate - - 3.0 Potassium orthophosphate 7.0 5.0 4.0 Copolymer of maleic anhydride and vinyl methyl ether (1::1) 0.5 0.5 0.5 Dimerised oleic acid (K salt) 1 5.0 5.0 5.0 Sodium carboxymethylcellulö 9;6 0.6 0.6 Sodium alkaline - silicate 5.0 5.0 5.0 Fluorescent agents 0.3 0.3 0.3 Blue dye 0.02 0.02 0.02 Perfume -0.3 0.3 0.3 Water to to to 100.0 100.0 100.0 1 Calculated in acid form These compositions were prepared by firstly reacting the maleic anhydride copolymer with an equal amount of the nonionic detergent compound in water at 80"C.
Then more water was added with potassium hydroxide, followed by the alkyl benzene sulphonate and dimerised oleic acid which were neutralised by the potassium hydroxide. The remaining nonionic detergent compound and minor ingredients were then added, followed by the two phosphate salts and lastly the silicate. The products of these Examples had acceptable viscosities of 450 cp, 700 and 950 cp at room temperature (Brookfield Spindle No. 3, 30 rpm), and they were all about pH 12.5 (undiluted).
The detergencies of the compositions were determined in a Terg-O-Tometer at 50"C and it was found that the compositions of Examples 4 and 5 were particularly good, being superior to a comparative product which contained 21% sodium tripolyphosphate, i.e. about the maximum level of that material which could be used in a stable aqueous liquid composition as the sole detergency builder.
WHAT WE CLAIM IS: 1. An aqueous, heterogeneous, stable liquid detergent composition comprising a) from 2-20% by weight of a detergent active material selected from anionic, nonionic, amphoteric, zwitterionic syn thetic detergents, soaps of C;,-C,, fatty acids, soaps of dimerized Cln-C22 fatty acids, and mixtures thereof; b) at least 2% by weight of sodium tripoly phosphate; c) at least 2% by weight of sodium or potassium orthophosphate, the sum of b) and c) being from 5-35% by weight; d) 0.1-2% by weight of a copolymer of
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (9)

**WARNING** start of CLMS field may overlap end of DESC **. parts are then blended together to give a suspended liquid system. Alternatively, compositions of higher sodium tripolyphosphate content in particular may be made by firstly dissolving a preformed copolymeric stabilising agent in water and partly esterifying the copolymer with some nonionic detergent active compound, adding the anionic detergent active compounds, any soap and any further nonionic compound to the resultant mixture, and then adding the phosphate salts and any sodium silicate.The heat of reaction between acidic and alkaline ingredients may be used to raise the temperature and facilitate mixing of the ingredients. The resultant compositions have viscosities in the range from 50 to 2,000 centipoise, especially 100 to 1500 centipoise, as measured at room temperature in a Brookfield viscometer (Spindle No. 3, 30 rpm). The invention is illustrated by the following Examples in which parts and percentages are by weight except where otherwise indicated. Example I and 2 Two stable heterogeneous liquid compositions were made to the following formulations: Ingredient Percentages Ex I Ex 2 Sodium alkyl (C3-,) benzene sulphonate 6 6 Tallow alcohol - 18 EO 2 2 Alkyl phosphate 1 1 Dimerised oleic acid 2 2 Coconut ethanolamide - - Sodium tripolyphosphate 10 10 Sodium orthophosphate 8 8 Stabilising agent 3 1 1 Water . 72 71 1 Obtained as Hostaphat Obtained as Empol, neutralised to the sodium salt in processing 1 Copolymer of maleic anhydride with vinyl methyl ether 1::1, obtained as Gantrez AN 119, hydrolysed and neut rallised in processing The composition of Examples 1 and 2 had low sudsing properties due to the alkyl phosphate or the dimerised fatty acid, and were suitable for use in front loading automatic washing machines. In these examples, the combined amount of sodium tripolyphosphate and sodium orthophosphate were equivalent in hard water detergency building properties to a level of about 35% of sodium tripolyphosphate alone, which of course is more than could be included into a stable aqueous liquid detergent composition. Examples 3 to 5 Three stable, heterogeneous built liquid detergent compositions were prepared to the following formulations: Ingredient Percentages Vex 3 Ex4 Ex5 Alkanol (C31 -C15) - 11 EO 2.5 2.5 2.5 Potassium alkylbenzene 1 sulphonate 6.5 6.5 6.5 Sodium tripolyphosphate 11.0 16.0 18.0 Potassium tripolyphosphate - - 3.0 Potassium orthophosphate 7.0 5.0 4.0 Copolymer of maleic anhydride and vinyl methyl ether (1::1) 0.5 0.5 0.5 Dimerised oleic acid (K salt) 1 5.0 5.0 5.0 Sodium carboxymethylcellulö 9;6 0.6 0.6 Sodium alkaline - silicate 5.0 5.0 5.0 Fluorescent agents 0.3 0.3 0.3 Blue dye 0.02 0.02 0.02 Perfume -0.3 0.3 0.3 Water to to to 100.0 100.0 100.0
1 Calculated in acid form These compositions were prepared by firstly reacting the maleic anhydride copolymer with an equal amount of the nonionic detergent compound in water at 80"C.
Then more water was added with potassium hydroxide, followed by the alkyl benzene sulphonate and dimerised oleic acid which were neutralised by the potassium hydroxide. The remaining nonionic detergent compound and minor ingredients were then added, followed by the two phosphate salts and lastly the silicate. The products of these Examples had acceptable viscosities of 450 cp, 700 and 950 cp at room temperature (Brookfield Spindle No. 3, 30 rpm), and they were all about pH 12.5 (undiluted).
The detergencies of the compositions were determined in a Terg-O-Tometer at 50"C and it was found that the compositions of Examples 4 and 5 were particularly good, being superior to a comparative product which contained 21% sodium tripolyphosphate, i.e. about the maximum level of that material which could be used in a stable aqueous liquid composition as the sole detergency builder.
WHAT WE CLAIM IS: 1. An aqueous, heterogeneous, stable liquid detergent composition comprising a) from 2-20% by weight of a detergent active material selected from anionic, nonionic, amphoteric, zwitterionic syn thetic detergents, soaps of C;,-C,, fatty acids, soaps of dimerized Cln-C22 fatty acids, and mixtures thereof; b) at least 2% by weight of sodium tripoly phosphate; c) at least 2% by weight of sodium or potassium orthophosphate, the sum of b) and c) being from 5-35% by weight; d) 0.1-2% by weight of a copolymer of
maleic anhydride with ethylene, styrene or vinylmethylether in an aqueous medium.
2. A composition according to claim 1, comprising 5-15% of a); at least 4% of b); at least 4% of c), the sum of b) and c) being from 10-30% by weight; and 0.3-1.5% of d).
3. A composition according to claim 1 or 2, wherein the weight ratio of b) to c) is from 10:1 to 1:10.
4. A composition according to claims 3, wherein the weight ratio of b) to e) is from 4:1 to 2:3.
5. A comDeJ;,ion according to claim 4, wilerem the weight ratio of b) to c) is from 3:1 to 1:1.
6. A composition according to claims 1-5, wherein the sodium tripolyphosphate contains more than 50% by weight of phase I sodium tripolyphosphate.
7. A composition according to claims 1-6, wherein the copolymer d) is a copolymer of maleic anhydride with vinylmethylether in a molar ratio of 1:1.
8. A composition according to claims 1-7, further comprising an alkaline buffer.
9. A composition as claimed in claims 1-8, substantially as described in the Examples.
GB21428/76A 1976-05-24 1976-05-24 Liquid detergent compositions Expired GB1577120A (en)

Priority Applications (20)

Application Number Priority Date Filing Date Title
GB21428/76A GB1577120A (en) 1976-05-24 1976-05-24 Liquid detergent compositions
GR53505A GR63137B (en) 1976-05-24 1977-05-19 Liquid detergent compositions
FI771609A FI771609A (en) 1976-05-24 1977-05-20
DE2722988A DE2722988C2 (en) 1976-05-24 1977-05-20 Liquid detergents
AT0367377A AT362851B (en) 1976-05-24 1977-05-23 LIQUID DETERGENT
FR7715791A FR2352878A1 (en) 1976-05-24 1977-05-23 NEW LIQUID DETERGENT COMPOSITIONS
BR7703301A BR7703301A (en) 1976-05-24 1977-05-23 LIQUID DETERGENT COMPOSITION
SE7706014A SE433087B (en) 1976-05-24 1977-05-23 Aqueous, aqueous, liquid detergent composition
CH634277A CH628370A5 (en) 1976-05-24 1977-05-23 Aqueous, heterogeneous, stable, liquid detergent
JP5969777A JPS52146407A (en) 1976-05-24 1977-05-23 Liquid detergent composition
DK225777A DK148100C (en) 1976-05-24 1977-05-23 Heterogeneous, watery, liquid detergent
BE177798A BE854906A (en) 1976-05-24 1977-05-23 NEW LIQUID DETERGENT COMPOSITIONS
ZA00773065A ZA773065B (en) 1976-05-24 1977-05-23 Liquid detergent compositions
NO771785A NO771785L (en) 1976-05-24 1977-05-23 WATER, HETEROGENE, LIQUID DETERGENT MIXTURE
IT7768176A IT1083001B (en) 1976-05-24 1977-05-23 LIQUID DETERGENT COMPOSITION PARTICULARLY FOR WASHING OF FABRICS
NL7705673A NL7705673A (en) 1976-05-24 1977-05-24 METHOD FOR THE PREPARATION OF LIQUID DETERGENTS.
LU77404A LU77404A1 (en) 1976-05-24 1977-05-24
CA278,973A CA1100382A (en) 1976-05-24 1977-05-24 Liquid detergent compositions
PT66595A PT66595B (en) 1976-05-24 1977-05-24 Liquid detergent compositions
ES459099A ES459099A1 (en) 1976-05-24 1977-05-24 Liquid detergent compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB21428/76A GB1577120A (en) 1976-05-24 1976-05-24 Liquid detergent compositions

Publications (1)

Publication Number Publication Date
GB1577120A true GB1577120A (en) 1980-10-22

Family

ID=10162794

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21428/76A Expired GB1577120A (en) 1976-05-24 1976-05-24 Liquid detergent compositions

Country Status (20)

Country Link
JP (1) JPS52146407A (en)
AT (1) AT362851B (en)
BE (1) BE854906A (en)
BR (1) BR7703301A (en)
CA (1) CA1100382A (en)
CH (1) CH628370A5 (en)
DE (1) DE2722988C2 (en)
DK (1) DK148100C (en)
ES (1) ES459099A1 (en)
FI (1) FI771609A (en)
FR (1) FR2352878A1 (en)
GB (1) GB1577120A (en)
GR (1) GR63137B (en)
IT (1) IT1083001B (en)
LU (1) LU77404A1 (en)
NL (1) NL7705673A (en)
NO (1) NO771785L (en)
PT (1) PT66595B (en)
SE (1) SE433087B (en)
ZA (1) ZA773065B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2158453A (en) * 1984-04-06 1985-11-13 Colgate Palmolive Co Liquid laundry detergent composition containing polyphosphate
LT3962B (en) 1993-12-21 1996-05-27 Albright & Wilson Funcional fluids

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3065073D1 (en) * 1979-11-09 1983-11-03 Unilever Nv Non-aqueous, built liquid detergent composition and method for preparing same
ZA83769B (en) * 1982-02-05 1984-09-26 Albright & Wilson Liquid detergent compositions

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3021284A (en) * 1958-10-30 1962-02-13 Atlantic Refining Co Liquid detergent compositions
BE606832A (en) * 1960-08-02
BE624160A (en) * 1961-10-30
GB1237874A (en) * 1967-07-19 1971-06-30 Unilever Australia Proprietary Detergent composition
GB1412401A (en) * 1971-09-02 1975-11-05 Unilever Ltd Detergent compositions
GB1530799A (en) * 1975-08-28 1978-11-01 Unilever Ltd Detergent compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2158453A (en) * 1984-04-06 1985-11-13 Colgate Palmolive Co Liquid laundry detergent composition containing polyphosphate
AU573324B2 (en) * 1984-04-06 1988-06-02 Colgate-Palmolive Pty. Ltd. Polyphosphate-containing liquid detergent compositions
LT3962B (en) 1993-12-21 1996-05-27 Albright & Wilson Funcional fluids

Also Published As

Publication number Publication date
FI771609A (en) 1977-11-25
NL7705673A (en) 1977-11-28
DK148100C (en) 1985-09-02
GR63137B (en) 1979-09-18
ATA367377A (en) 1980-11-15
JPS52146407A (en) 1977-12-06
IT1083001B (en) 1985-05-21
AT362851B (en) 1981-06-25
DE2722988A1 (en) 1977-12-08
DK225777A (en) 1977-11-25
FR2352878B1 (en) 1980-05-16
FR2352878A1 (en) 1977-12-23
CA1100382A (en) 1981-05-05
NO771785L (en) 1977-11-25
PT66595B (en) 1979-04-13
DE2722988C2 (en) 1985-11-21
ZA773065B (en) 1979-01-31
LU77404A1 (en) 1977-12-22
BR7703301A (en) 1978-03-14
PT66595A (en) 1977-06-01
DK148100B (en) 1985-03-04
ES459099A1 (en) 1978-10-01
BE854906A (en) 1977-11-23
CH628370A5 (en) 1982-02-26
SE433087B (en) 1984-05-07
SE7706014L (en) 1977-11-25

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PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee