AU650247B2 - Suspending liquid detergent compositions - Google Patents

Suspending liquid detergent compositions Download PDF

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Publication number
AU650247B2
AU650247B2 AU66956/90A AU6695690A AU650247B2 AU 650247 B2 AU650247 B2 AU 650247B2 AU 66956/90 A AU66956/90 A AU 66956/90A AU 6695690 A AU6695690 A AU 6695690A AU 650247 B2 AU650247 B2 AU 650247B2
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AU
Australia
Prior art keywords
composition according
liquid detergent
detergent composition
weight
compound
Prior art date
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Ceased
Application number
AU66956/90A
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AU6695690A (en
Inventor
Francesco De Buzzaccarini
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Procter and Gamble Co
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Procter and Gamble Co
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Filing date
Publication date
Priority claimed from GB898926620A external-priority patent/GB8926620D0/en
Priority claimed from GB909009823A external-priority patent/GB9009823D0/en
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of AU6695690A publication Critical patent/AU6695690A/en
Application granted granted Critical
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Classifications

    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/08Polycarboxylic acids containing no nitrogen or sulfur
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0026Structured liquid compositions, e.g. liquid crystalline phases or network containing non-Newtonian phase
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Description

AUSTRALIA
Patents Act COMPLETE SPECIFICATION
(ORIGINAL)
Class Application Number: Lodged: Complete Specification Lodged: Accepted: Published: Priority Related Art: Int. Class247 Int. Class Applicant(s): The Procter Gamble Company One Procter Gamble Plaza, Cincinnati, Ohio 45202, UNITED STATES OF
AMERICA
Address for Service is: PHILLIPS ORMONDE FITZPATRICK Patent and Trade Mark Attorneys 367 Collins Street Melbourne 3000 AUSTRALIA Complete Specification for the invention entitled: SUSPENDING LIQUID DETERGENT COMPOSITIONS Our Ref 196680 POF Code: 44135/44135 The following statement is a full description of this invention, including the best method of performing it known to applicant(s): 16006 6006 C~-a3m A: SUSPENDING LIQUID DETERGENT COMPOSITIONS F. de BUZZACCARINI Technical Field The invention relates to aqueous built detergent compositions which are pourable, and have suspending properties.
Background Aqueous pourable detergent compositions are well known in the Art, but it is only recently that C10-C16 alk(en)yl substituted succinic acids have been used as builders in -these compositions, which have been disclosed in EP-A-0 293 040 and EP-A- 0 294 904.
These compositions are very satisfactory in terms of their cleaning performance, but ingredients in the form of solid particles could not be stably suspended in these compositions, and therefore it is recommended to use only liquid ingredients during their manufacture. Indeed, the 2 use of ingredients in the form of solid particles inevitably leads to sedimentation.
Pourable compositions having such suspending properties have been disclosed for instance in EP-A -0 151 884, EP-A-0 120 638, EP-A-0 092 363, GB-A-2 023 637, US-A-4 692 271; all the compositions disclosed in these documents do not contain C 10
-C
16 alk(en)yl substituted succinic acids, and it has been found that said compositions would lose their suspending properties upon incorporation of said substituted succinic acids.
It is an object of the present invention to provide aqueous, pourable detergent compositions, which contain C1 0
-C
16 alk(en)yl substituted succinic acids and which further have suspending properties.
Further, the compositions of the prior art tend to collapse also if hydrophilic solvents are incorporated in important amounts; it is another object of the present invention to provide aqueous, pourable detergent compositions, which contain C 10
-C
16 alk(en)yl substituted succinic acids and have suspending properties, and which may further contain hydrophilic solvents, such as ethanol.
Summary It has now been found that aqueous, pourable detergent composition containing an anionic surfactant and
C
10
-C
16 alk(en)yl substituted succinic acid could acquire suspending properties by formulating them as neat phases, by incorporating at least about 7.5% by weight of the total composition of a compound of the formula
RO(CH
2
CH
2 0)yH wherein: R is a Cn alkyl, alkenyl, alkynyl, aryl or alkyl aryl group and n is an integer of from 4 to 22 and y 0 to 4 and n/y 2 if y 4 0 Applicants have surprisingly found that if they select a compound of the above formula and incorporate it into the total composition in the above amount, a neat phase is formed.
Detailed Description of the Invention Accordingly, in a first aspect of the present invention there is provided a liquid detergent composition including from 5% to 60% by weight of surfactant wherein said surfactant includes anionic surfactant and optionally one or more zwitterionic or cationic surfactants; from 5% to 20% by weight of a C 10
-C
16 alk(en)yl substituted succinic acid; and from 20% to 60% by weight water; said compositions being formulated as a heat phase by further including at least 7.5% by weight of the total composition of a compound of the formula
RO(CH
2
CH
2 0)yH wherein: R is a Cn alkyl, alkenyl, alkynyl, aryl or alkyl aryl group and n is an integer of from 4 to 22 and y 0 to 4 and n/y 2 if y t 0 and mixtures thereof.
The present invention addresses the problem of formulating an aqueous detergent composition which contains C 1 0 -Cle alk(en)yl substituted succinic acids, and which has suspended properties.
It has been found that such composition can be formulated as a neat phase as fo follows. In the following, the expression neat phase (or G-phase) refers to an S essentially lamella-structured or spherulitic composition in which aqueous layers are separated by double layers of hydrophobic materials. Such a lamellar structure can be I-a 3A identified by observing the product through an optical microscope, between crossed Nichol prisms.
The neat phases are characterized by specific textures which are described for instance by F.B. Rosevear, journal of the American Oil Chemists Society, vol. 3, page 628, 1954.
aL3^ L ill 4 The compositions of the invention always contains an anionic surfactant.
Suitable anionic surfactants can be represented by the general formula R 1
SO
3 M wherein R 1 represents a hydrocarbon group selected from the group consisting of straight or branched alkyl radicals containing from about 8 to about 24 carbon atoms and alkyl phenyl radicals containing from about 9 to about 15 carbon atoms in the alkyl group. M is a salt forming cation which typically is selected from the group consisting of sodium, potassium, ammonium, and mixtures thereof.
A preferred synthetic anionic surfactant is a water-soluble salt of an alkylbenzene sulfonic acid containing from 9 to 15 carbon atoms in the alkyl group.
Another preferred synthetic anionic surfactant is a water-soluble salt of an alkyi sulfate or an alkyl polyethoxylate ether sulfate wherein the alkyl group contains from about 8 to 24, preferably from about 10 to about 18 carbon atoms and there are from about 1 to about preferably from about 1 to about 12 ethoxy groups.
Other suitable anionic surfactants are disclosed in US Patent 4,170,565, Flesher et al., issued October 9, 1979.
Suitable anionic synthetic surface-active salts are selected from the group of sulfonates and sulfates.
Preferred anionic synthetic water-soluble sulfonate or sulfate salts have in their molecular structure an alkyl radical containing from about 8 to about 22 carbon atoms.
Exemples of such preferred anionic surfactant salts are the reaction products obtained by sulfating C 8
-C
18 fatty alcohols derived from tallow and coconut oil; 5 alkylbenzene sulfonates wherein the alkyl group contains from about 9 to 15 carbon atoms; sodium alkylglyceryl ether sulfonates; ether sulfates of fatty alcohols derived from tallow and coconut oils; coconut fatty acid monoglyceride sulfates and sulfonates; and water-soluble salts of paraffin sulfonates having from about 8 to about 22 carbon atoms in the alkyl chain. Sulfonated olefin surfactants as more fully described in e.g. US Patent Specification 3,332,880 can also be used. The neutralizing cation for the anionic synthetic sulfonates and/or sulfates is represented by conventional cations which are widely used in detergent technology such as sodium and potassium.
A particularly preferred anionic synthetic surfactant component herein is represented by the water-soluble salts of an alkylbenzene sulfonic acid, preferably sodium alkylbenzene sulfonates having from about 10 to 13 carbon atoms in the alkyl group.
The compositions of the invention may additionally contain zwitterionic surfactants which include derivatives of aliphatic quaternary ammonium, phosphonium, and sulphonium compounds in which the aliphatic moiety can be straight or branched chain and wherein one of the aliphatic substituents contains from about 8 to about 24 carbon atoms and another substituent contains, at least, an anionic water-solubilizing group. Particularly preferred zwitterionic materials are the ethoxylated ammonium sulfonates and sulfates disclosed in US Patents 3,925,262, Laughlin et al., issued December 9, 1975 and 3,929,678, Laughlin et al., issued December 30, 1975.
The compositions may also contain small amounts, i.e.
below about 1% by weight of the total composition, of cationic -1 i 6 surfactants. Examples of suitable cationic surfactants include quaternary ammonium compounds of the formula
R
1
R
2
R
3
R
4 N+X wherein R1 is C 1 2
-C
2 0 alkyl or hydroxyalkyl;
R
2 is C 1
-C
4 alkyl or C12-C 2 0 alkyl or hydroxyalkyl or C 1
-C
4 hydroxyalkyl; R 3 and R4 are each C 1
-C
4 alkyl or hydroxyalkyl, or C6-Cg aryl or alkylaryl; and X- is halogen. Preferred are mono-long chain quaternary ammonium compounds compounds of the above formula wherein R2 is C1-C4 alkyl or hydroxyalkyl).
The total amount of surfactant in the compositions is of from about 5% to about 60%, preferably about 15% to about 40% by weight of the total composition.
The compositions of the invention additionally contain at least about 7,5% of a compound of the formula RO (CH2CH) yH wherein R is a C n alkyl, alkenyl, alkynyl, aryl or alkyl aryl group n is an integer of from 4 to 22 y 0 to 4 and n/y 2 2 if y 0 or mixtures thereof.
Preferred compounds according to this definition are condensation products of ethylene oxide with a fatty alcohol in the presence of an acidic or basic catalyst.
Preferably, fatty alcohols having from 13 to 15 carbon atoms are used to make such condensation product.
Also preferred are such solvents as butanol, butoxyethanol, benzylalcohol, hexyl diglycol ether, butyl diglycolether, and mixtures thereof.
r~ II 7 The compounds are present in the compositions of the invention in an amount of at l-ast about 7,5% by weight of the total composition, preferably from about 8% to about by weight.
The compositions of the invention also contain as a builder system, from about 5% to about 20% by weight of the total composition of a C 1 0
-C
1 6 alk(en)yl substituted succinic acid, preferably from about 8% to about 15% by weight of the total composition. The preferred builder for use herein is dodecenyl substituted succinic acid.
Importantly, the compositions of the invention contain water, in an amount of from about 20% to about 60% by weight of the composition.
All the hereinbefore mentioned ingredients are mixed together so as to obtain a compositon which is structured as a neat phase.
Optionally, the compositions of the invention may contain an electrolyte such as sodium bromide, chloride, iodide, nitrate or acetate, preferably sodium chloride.
Other optionals include detergent enzymes. Suitable enzymes include the detergent proteases, amylases, lipases and cellulases. Enzymatic stabilizing agents for use in aqueous liquid detergents which are well known, can also be used herein; preferred is a salt of formic acid, e.g., sodium formate. The amount of this stabilizing agent typically ranges from about 0.5% to about 2%.
Examples of organic builders are represented by polyacids such as citric acid, nitrilotriacetic acid, and mixtures of tartrate monosuccinate with tartrate ui-7- slr~-- I 8 disuccinate. Preferred builders for use herein are citric acid. Polymeric carboxylate builders inclusive of polyacrylates, polydydroxy acrylates and polyacrylates/ polymaleates copolymers can also be used.
The compositions of the invention may also contain chelants, such as ethylenediaminotetracetic acid, diethylenetriaminopentacetic acid, ethylenediamino disuccinic acid or the water-soluble alkali metals thereof. Other additives include organo-phosphonic acids; particularly preferred are ethylenediamino tetramethylenephosphonic acid, hexamethylenediamino tetrametylenephosphonic acid, diethylenetriamino pentamethylenephosphonic acid, aminotrimethylenephosphonic acid and hydroxyethylidene 1,1 diphosphonic acid.
The compositions herein can contain further optional ingredients which are mostly used in additive levels, usually below about Examples of the like additives include Suds regulants, opacifiers, agents to improve the machine compatibility in relation to enamel-coated surfaces, bactericides, dyes, perfumes, brighteners and the like.
The beneficial utilization of the claimed compositions under various usage conditions can require the utilization of a suds regulant like polysiloxanes such as dimethylpolysiloxane, also frequently termed silicones.
These silicones ate frequently used in a level not exceeding about most preferably between about 0.1% and about It can also be desirable to utilize opacifiers inasmuch as they contribute to create a uniform appearance of the 9 concentrated liquid detergent compositions. Examples of suitable opacifiers include polystyrene commercially known as LYTRON 621 manufactured by MONSANTO CHEMICAL CORPORATION. The opacifiers are frequently used in an amount from about 0.3% to about It can further be desirable to add from about 0.1% to about 5% of known antiredeposition and/or compatibilizing agents.
Examples of the like additives include sodium carboxymethylcellulose; hydroxy-Cl-6-alkylcellulose; polycarboxylic homo- or copolymeric ingredients, such as polymaleic acid; a copolymer of maleic anhydride and methylvinylether in a molar ratio of 2:1 to 1:2; and a copolymer of an ethylenically unsaturated monocarboxylic acid 'onomer, having not more than 5, preferably 3 or 4 carboin atoms, for example (meth)acrylic acid, and an ethylenically unsaturated dicarboxylic acid monomer having not more than 6, preferably 4 carbon atoms, whereby the molar ratio of the monomers is in the range from 1:4 to 4:1, said copolymer being described in more detail in EUROPEAN Patent Application 0 066 915, filed May 17, 1982.
Since the compositions of the invention have acquired suspending properties, due to the formulation as a neat phase, it is possible to use ingredients which are in the form of solid particles. There is no r striction as to tle nature of the ingredient, but these ingredients are preferably in the form of solid particles having an average diameter size in the range of from about 1 micrometer to about 350 micrometers.
Such ingredients can be zeolites, clays, suds suppressors such as silica waxes, any encapsulated material, and a highly preferred ingredient to be suspended 10 in the compositions are solid, water-soluble peroxygen bleaching compounds, preferably perborates, persulfates, peroxydisulfates, perphosphates and the crystalline peroxyhydrates formed by reacting hydrogen peroxide with sodium carbonate or urea. Preferred are sodium perborate, monohydrate and tetrahydrate, and sodium percarbonate.
If a peroxygen bleaching compound is used, the compositions preferably contain water miscible organic solvents including ethanol, n-propanol, isopropanol polyethylene glycol, dipropylene glycol, hexylene glycol, methoxyethanol, ethoxyethanol, ethyldiglycolether, and mixtures thereof. Preferably, the compositions will contain fromL to l-9A of the total composition of ethanol, as a stabilizing system for the peroxygen compounds.
Also, in such a case, the pH as is of the compositions -should-be.jin the range of from about 8 to about 12, preferably about 9 to about 11.
The following examples will illustrate and facilitate the understanding of the invention, but are not meant to restrict its scope.
Examples The following composition are obtained by mixing together the listed ingredients in the listed proportions.
(LAS stands for linear alkyl benzene suphonate, CnAS stands for coconut alkyl sulfate, TAS stands for tallow alkyl sulfate and DTMPA stands for diethylene triamine _pentamethylene phosphonic acid.) v,\ J" 11 The order in which the ingredients are mixed plays no role in the achievement of the neat phase structure; it is however particularly convenient to proceed as follows, referring to example IV.
A premix which is made with water, DTMPA and citric acid is neutralized to pH 7 with sodium hydroxide. The solvents (ethanol and hexyl diglycolether) are then added.The linear alkyl benzene sulfonate and the dodecenyl substituted succinic acid are added while cooling the mixture; the pH is then trimmed to 10 with sodium hydroxide. The composition at this point is not yet a neat phase, but an isotropic solution characterized by its low viscosity and transparency. The neat phase which is formed on adding the C 14 alcohol 3 times ethoxylated can be identified by a higher viscosity and a translucent appearance; to confirm the formation of the neat phase structure, the composition can be examined with an optical microscope, between crossed Nichol prisms.
The sodiura chloride and all minor ingredients are finally incorporated in the composition.
If an ingredient in the form of solid particles is to be incorporated, it is preferable to do so before the formation of the neat phase, in order to facilitate the mixing.
Compositions (Comp.). (Comp) (Comp.) I II III IV V by weight (Comp.) Cm Co'.Y VI VII VIII IX Ingredients Linear alkyl benzene sulphonate Coconut alkyl sulfate Tallow alkyl sulfate Dodecyl succinic acid C13 alcohol 5 ethoxylated Diethylene triamine pentamethylene phosphonic acid Hexyl diglycol ether Butyl diglycol ether C14 alcohol 3 ethoxylated Oleyl alcohol Sodium chloride Ethanol Citric acid Sodium perborate tetrahydrate Sodium percarbonate Sodium hydroxide (to pH) Water, perfume, minors 10.0 0.0 0.0 5.6 0.5 0.0 35.0 0.0 0.0 0.0 0.0 0.0 0.5 0.0 0.0 9.0 9.0 0.0 0.0 11.0 7.0 0.0 15.0 0.0 0.0 0.0 3.0 1.0 2.5 0.0 0.0 9.0 9.0 0.0 0.0 11.0 7.0 0.0 4.0 0.0 0.0 11.0 0.0 3.0 2.5 0.0 0.0 9.0 9.0 0.0 0.0 11.0 0.0 0.5 4.0 0.0 11.0 0.0 2.0 3.0 2.5 0.0 0.0 9.0 9.0 0,0 0.0 11.0 0.0 0.5 0.0 0.0 22.0 0.0 0.0 3.0 2.5 0.0 0.0 9.0 9.0 0.0 0.0 11.0 7.0 0.5 0.0 0.0 19.0 0.0 7.5 2.0 2.5 0.0 0.0 9.0 0.0 0.0 0.0 11.0 7.0 0.5 0.0 7.5 0.0 0.0 0.0 7.0 2.5 15.0 0.0 10.0 9.0 0.0 0.0 11.0 0.0 0.5 0.0 5.0 7.0 0.0 4.0 7.0 2.5 22.0 0.0 10.0 0.0 0.0 11.0 0.0 0.0 0.0 0.0 20.0 10.0 to 100 to 100 to 100 to 100 to 100 to 100 to 100 to 100 to 100 Comp. Compatative Copsitions Ingfredients %by weight Linear alkyl benzene suiphonate 14.0 10.4 0.0 0.0 Coconut alkyl sulfate 0.0 0.0 10.0 0.0 Tallow alkyl. suiphonate 6 0 0.0 0.0 Dodecyl succinic a,.-id 9.5 10.0 8.0 C13 alcohol 5 ethoxylated 5.0 5.0 0.0 0.0 Diethylene triamine pentainethylene pVsphonic acid 0.0 0.0 0.0 0.0 Hexyl. diglycol ether 0.0 0.0 0.0 0.0 Butyl diglycol. ether 7.0 6.5 6.0 C14 alcohol 3 ethoxylated 2.5 2.5 10.0 15.0 Oleyl alcohol 0.0 9.5 0.0 0.0 Sodium chloride 5.0 0.0 5.0 Ethanol 4.0 2.5 2.0 Citric acid 2.5 2.5 2.0 Sodium perborate tetrahydrate 21.0 0.0 21.0 0.0 Sodium percarbonate 0.0 0.0 0.0 0.0 Sodium hydroxide (to pH) 9.5 9.5 9.5 Water, perfume, minors to 100 to 100 *to 100 to 100

Claims (14)

1. A liquid detergent composition including from to 60% by weight of surfactant wherein said surfactant includes anionic surfactant and optionally one or more zwitterionic or cationic surfactants; from 5% to 20% by weight of a C10-C16 alk(en)yl substituted succinic acid; and from 20% to 60% by weight water; said compositions being formulated as a neat phase by further including at least 7.5% by weight of the total composition of a compound of the formula RO(CH 2 CH 2 0) yH wherein: R is a C alkyl, alkenyl, alkynyl, aryl or alkyl aryl group and n is an integer of from 4 to 22 and y 0 to 4 and n/y 2 if y 1 0 and mixtures thereof.
2. A liquid detergent composition according to claim 1, including from 8% to 15% by weight of the total composition of a C 10 -C 1 6 alk(en)yl substituted succinic acid.
3. A liquid detergent composition according to claim 1 or 2, wherein the compound is selected from butyl diglycol ether, hexyl diglycol ether and the condensation products of C13-C15 fatty alcohols with 3 moles of ethylene oxide per mole of fatty alcohol, or mixtures thereo..
4. A liquid detergent composition according to any one of claims 1 to 3, wherein said compound is present in an amount of from 8% to 15% by weight of the total composition.
A liquid composition according to any one of 3' claims 1 to 4, further including up to about 10% by weight of the total composition of an electrolyte.
6. A liquid composition according to claim 5, wherein the electrolyte is sodium chloride. S- 14
7. A liquid detergent composition according to any one of claims 1 to 6, further including at least one ingredient which is in the form of solid particles.
8. A liquid composition according to claim 7, wherein said ingredient is a peroxygen compound.
9. A liquid detergent composition according to claim 8, wherein the peroxygen compound is in the form of particles having a diameter size in the range of from 1 micrometer to 350 micrometer.
10. A liquid detergent composition according to any one of claims 8 or 9, wherein said peroxygen compound is a perborate.
11. A liquid detergent composition according to any one of claims 8 or 9, wherein said peroxygen compound is a 13 percarbonate.
12. A liquid detergent composition according to any one of claims 1 to 11, further including from 3% to 12% by weight of the total composition of ethanol.
13. A light detergent composition according to any one of claims 1 to 12 which has a pH of at least about 9.
14. A liquid detergent composition according to claim 1 substantially as hereinbefore described with reference to the examples. DATED: 18 March, 1994 PHILLIPS ORMONDE FITZPATRICK U5 dLi Attorneys for: THE PROCTER GAMBLE COMPANY 6016V 15
AU66956/90A 1989-11-24 1990-11-23 Suspending liquid detergent compositions Ceased AU650247B2 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB8926620 1989-11-24
GB898926620A GB8926620D0 (en) 1989-11-24 1989-11-24 Suspending liquid detergent compositions
GB909009823A GB9009823D0 (en) 1990-04-27 1990-04-27 Suspending liquid detergent compositions
GB9009823 1990-04-27

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AU6695690A AU6695690A (en) 1991-05-30
AU650247B2 true AU650247B2 (en) 1994-06-16

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AR (1) AR245207A1 (en)
AU (1) AU650247B2 (en)
BR (1) BR9005930A (en)
CA (1) CA2030205C (en)
IE (1) IE904243A1 (en)
MX (1) MX172443B (en)
NZ (1) NZ236205A (en)
PE (1) PE31191A1 (en)
TR (1) TR25074A (en)

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IN185580B (en) * 1991-08-30 2001-03-03 Albright & Wilson Uk Ltd
GB2259519B (en) * 1991-08-30 1996-03-06 Albright & Wilson Concentrated aqueous surfactant compositions
EP0619368A1 (en) * 1993-04-06 1994-10-12 The Procter & Gamble Company Concentrated liquid detergent compositions
US6194364B1 (en) 1996-09-23 2001-02-27 The Procter & Gamble Company Liquid personal cleansing compositions which contain soluble oils and soluble synthetic surfactants
DE19851662A1 (en) * 1998-11-10 2000-05-18 Menno Chemie Vertriebsges M B Means for removing the adhesiveness of helminth eggs
US6897188B2 (en) 2001-07-17 2005-05-24 Ecolab, Inc. Liquid conditioner and method for washing textiles
US8110537B2 (en) 2003-01-14 2012-02-07 Ecolab Usa Inc. Liquid detergent composition and methods for using
US7682403B2 (en) 2004-01-09 2010-03-23 Ecolab Inc. Method for treating laundry
JP4864598B2 (en) * 2006-08-11 2012-02-01 花王株式会社 Cleaning composition for hard surface
EP4296345A3 (en) 2017-06-22 2024-03-13 Ecolab USA Inc. Bleaching using peroxyformic acid and an oxygen catalyst

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EP0430330A3 (en) 1991-12-18
BR9005930A (en) 1991-09-24
NZ236205A (en) 1993-10-26
AR245207A1 (en) 1993-12-30
PE31191A1 (en) 1991-11-09
MX172443B (en) 1993-12-16
CA2030205A1 (en) 1991-05-25
IE904243A1 (en) 1991-06-05
JPH03210400A (en) 1991-09-13
TR25074A (en) 1992-11-01
CA2030205C (en) 1995-11-21
AU6695690A (en) 1991-05-30
EP0430330A2 (en) 1991-06-05

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