IE904243A1 - Suspending liquid detergent compositions - Google Patents

Suspending liquid detergent compositions

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Publication number
IE904243A1
IE904243A1 IE424390A IE424390A IE904243A1 IE 904243 A1 IE904243 A1 IE 904243A1 IE 424390 A IE424390 A IE 424390A IE 424390 A IE424390 A IE 424390A IE 904243 A1 IE904243 A1 IE 904243A1
Authority
IE
Ireland
Prior art keywords
detergent composition
composition according
weight
detergent
compound
Prior art date
Application number
IE424390A
Original Assignee
Procter & Gamble
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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 & Gamble filed Critical Procter & Gamble
Publication of IE904243A1 publication Critical patent/IE904243A1/en

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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

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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)
  • Crystallography & Structural Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

Pourable aqueous detergent compositions containing C₁₀-C₁₆ alk(en)yk substituted succinic acid as a builder, are formulated as neat phases.

Description

The invention relates to aqueous built detergent compositions which are pourable, and have suspending properties.
Aqueous pourable detergent compositions are well known in the Art, but it is only recently that C10-C16 alk(en)yl substituted succinic acids huve 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 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 C10-C16 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 c10-c16 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 ciq-ci6 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 c10-c16 alk(en)yl substituted succinic acid could acquire suspending properties by formulating them as neat phases, by incorporating at least 7.5% by weight of the total composition of a compound of the formula RO(CH2CH2O)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 =f= 0 Detailed Description of the Invention The present invention addresses the problem of formulating an aqueous detergent composition which contains c10-c16 alk(en)yl substituted succinic acids, and which has suspending properties.
It has been found that such composition can be formulated as a neat phase as follows. In the following, the expression neat phase (or G-phase) refers to an essentially lamella-structured or spherulitic composition in which aqueous layers are separated by double layers of hydrophobic materials.
Such a lamellar structure can be 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.
The compositions of the invention always contains an anionic surfactant.
Suitable anionic surfactants can be represented by the general formula R^SO^M wherein R1 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 alkyl 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 20, 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 Cg-C18 fatty alcohols derived from tallow and coconut oil; 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 1% by weight of the total composition, of cationic surfactants. Examples of suitable cationic surfactants include quaternary ammonium compounds of the formula R1R2R3R4N+X~' wherein is ci2-C20 alKyl or hydroxyalkyl; R2 is Cj-C^ alkyl or C12-C20 alkyl or hydroxyalkyl or Cj-C^ hydroxyalkyl; R3 and R4 are each C1-C4 alkyl or hydroxyalkyl, or C6-C8 aryl or alkylaryl; and X“ is halogen. Preferred are mono-long chain quaternary ammonium compounds (i.e., compounds of the above formula wherein R2 is C^-C^ alkyl or hydroxyalkyl).
The total amount of surfactant in the compositions is of from 5% to 60%, preferably 15% to 40% by weight of the total composition.
The compositions of the invention additionally contain at least 7,5% of a compound of the formula RO(CH2CH2O)yH wherein - R is a Cn 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 if y =f= θ 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.
The compounds are present in the compositions of the invention in an amount of at least 7,5% by weight of the total composition, preferably from 8% to 15% by weight.
The compositions of the invention also contain as a builder system, from 5% to 20% by weight of the total composition of a Cj^o^ie alk(en)yl substituted succinic acid, preferably from 8% to 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 20% tp 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 0.5% to 2%.
Examples of organic builders are represented by polyacids such as citric acid, nitrilotriacetic acid, and mixtures of tartrate monosuccinate with tartrate 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 tetramethylenephosphonic 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 5%. 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 are frequently used in a level not exceeding 1.5%, most preferably between 0.1% and 1.0%.
It can also be desirable to utilize opacifiers inasmuch as they contribute to create a uniform appearance of the 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 0.3% to 1.5%.
It can further be desirable to add from 0.1% to 5% of known antiredeposition and/or compatibilizing agents. Examples of the like additives include : sodium carboxymethylcellulose; hydroxy-C^_g-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 monomer, having not more than 5, preferably 3 or 4 carbon 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 restriction as to the 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 1 micrometer to 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 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 from 4% to 10% 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 in the range of from 8 to 12, preferably 9 to 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.
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 TV.
A premix which is made with water, diethylene triamine pentamethylene phosphonic acid 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 C14alcohol 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 sodium 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.
Water, perfume, minors cn cn fT cn o w cn o a S’ CC g σ ο σ H n cn r o o ft 0 H- rt Q 1—* c Φ φ H- I-* Cu 0 0 H- £X & rt Q. ft cr & Φ ft X ft Φ CJ Oi I—* Ω I—1 3 H- H- η H· b( 0) H- ·< cr ft Φ I—1 o Ό Φ Q) H- 3 I—1 CU t-1 »< 3 O Ό o 3 cr § S' n 0 1—* I—1 4? £ c 0 3 *< t—' 0 Ω Ol Ol Φ 1—' Ω l·-1 rt 3 CT Ό CL Ό o> n I-· O H· H· 3 Φ O 0 O 0> ►< φ hf Φ n cr Ω cr 03 vQ Φ 3 cr cn H 0 rt b-1 Q. b( PJ b( H- I—1 0 0 t—' Φ 0 0 X* I-1 Φ X t~! Ω rt σ £X 0 O' H ·< *< tl H Ω K ·< O 0> 0 b( o n o cr rt Ω I-* b-1 X 3 1-( H- H· CJ 0 o o b( Ul H· I—1 H- σ o> Oi ι-· b-> cn H- 3 cn σ Ol 0 rt Φ Φ 'S. Qj Φ H· 0 cn 2 (D 3 Φ ft φ Φ cr 3 rt Ω t-> C 3 £J 3* rt ft o H- cr bh I—1 N ,___. rt O cr cr 3 3 o 0) (» Ml Φ rt Φ X Φ φ H- Φ X Ω ft 0 3 0 b( b( O ·< H· Φ rt Φ I—1 'S I—* Ol Φ Ό o CD Φ 0) SC rt n 3 rt ‘-1 Φ H- ft Φ Ol Ol 0» Ol ft VO o o o o o o o o u o o Ul o o o o H* o o o (jl o o o o o o o cn cn o o o o o ft KO o o NJ I-* CJ o o o H o xj t—· o o VO o • • • • • • • • • ui • • H • • • O o o in o o o o o • o o o o o H* O O o o Ct VO Ο O · o o o tsJCJOb-’OO^O . . . |_l . moo· ο ο ο o o -J I—1 O O <0 . |_1 . . . o · o o o o rt o kd o o NJ CJ NJ o H o o o Ι-» o o ω o o o Ul o o o o o o in o o o o o rt KO o o NJ CJ o o NJ o o o o Η» o o VO 0 Η» o o o Ul o o o o o o cn o o o o o o o KO o o ru NJ -J o o o o b-> o o VO o o o Ul o Ul o o o o Ul o • o o o o ft o H* NJ -J o o o o o Η» o o KD 0 O • in • • • • • • • • • • • • • o • in o o o o in o ui o • o o O Η» O o O o o ft f—1 o NJ NJ -J o xj in o o o Ι-» o o KD o o • NJ • 1 • • • • • • • 1-» • • • • σ • in o O o o o o Ul o • o o O K o o o o o I II III IV V VI VII VIII Ingredients % by weight rf I-* NJ o NJ Xj o xj Ul o o o H* o o KD 0 O O • • • • • • • • • • Η» • • • • • o in o o o O o o ui o • o o o Η* o o O cl l-l X s 3 r+ M O CL cn 0 CL rt Φ rt cn a Ci 3· rt w rt 3· cn 0 CL O 3 Φ o 3 $ rt a φ X 3 Φ ft σ 3- Φ n 3* CJ 5 CL Η 3 3 n 0 Ω cn c 3 f 3- 3 Φ 3· 3- 3 3· 3 3 3· 3J 3 rt Φ 3-« 0 tl Φ ι-! p 3 g 3· 3 c I—1 0) 3 3 3J 3 0) Ω O 3 3· 3 g Er g Ω 0 § 3 3 3ζ 3 3J £ c 0 3 3- 3 0) Ω CL CL Φ 31 Ω 3 rt 3 Ό 3* tl CL tl 0) Ω 3 0 3- 3- 3 Φ 0 3 3 3 Φ Φ 3 Φ Ω 3 Ω 3 iQ iQ Φ 3 CT cn 3* 3 r+ 3 h{ CL 3 0) 3 3- 3 O O 3 I—* Φ O c TT 3 Φ X* 3 Ω rt O' CL 0 3* 3 3; 3; tl 3 Ω 3J X 3; o 3 Φ 0 3 0 Ω Ω 3 rt Ω 3 3i 3 X 3 3 3- I-1 ω O O O 3 Ul 3- 3 Φ 3- σ 0) Cb I—1 3 Cfl 3- 3 cn σ cl 0 rt Φ Φ tl 3 Φ 3- C cn φ φ 3 Φ rt Φ Φ 3* 3 rt Ω 3 C 3 3 iu 3· rt rt 0 3- 3* T3 3 N 3· rt 0 3* fcr 3 3 0 3 3* ttl ω 3 rt Φ X Φ Φ 3· Φ X Ω O 3 3 0 0 3 3 Ω 3; 3- 3 rt Φ 3 3 *5 3 CL 3 Φ (fl tl 0» 0) ro 0» rt s rt Ω 3 rt Φ Φ 3· rt Φ CL CL Ο) CL rt <0 0 to tO ui 0 to 0 0 Ul 0 0 l·—* 0 • • l·-» 3 O O Ul 0 0 Ul 0 0 0 Ul 0 0 0 0 ui 0 0 0 ft 10 0 0 to to 0 K0 to σ» 0 0 σι Η» 0 0 3 0 « « • * • • ♦ • • ♦ • • o • • O H O O σι 0 0 σι ui 0 cn σι ui 0 0 o 0 0 0 £>· rt VD 0 tO to to σι 0 H σ» 0 0 0 a> 0 0 0 • • 0 0 • 3 0 0 Ul 0 • 0 0 0 o 0 0 o 0 0 0 0 0 0 0 ft 10 0 0 to H* ui 0 H GJ 0 0 0 10 03 0 0 0 H Ul 0 0 ui Ul 0 0 0 ui 0 0 0 0 0 0 0 ο

Claims (15)

1. A detergent composition comprising a anionic surfactant, from 5% to 20% by weight of the total composition of a C 10 -C 16 alk(en)yl substituted succinic acid, characterized in that it is formulated as a neat phase.
2. A detergent compositicis according to claim 1, characterized in that it comprises at least 7.5% by weight of the total composition of a compound of the formula RO(CH 2 CH 2 O)yH wherein : - R is a C n 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 | 0 and mixtures thereof.
3. A detergent composition according to claim 1 or 2, characterized in that it comprises from 6% to 15% by weight of the total composition of a CjQ-C^g alk(en)yl substituted succinic acid.
4. A detergent composition according to claims 2 or 3, wherein the compound is selected from butyl diglycol ether, hexyl diglycol ether and the condensation products of C 13 -Cis fatty alcohols with 3 moles of ethylene oxide per mole of fatty alcohol, or mixtures thereof.
5. A detergent composition according to claims 2, 3 or 4, wherein said compound is present in an amount of from 8% to 15% by weight of the total composition.
6. A detergent composition according to any of the preceding claims, characterized in that it contains up to 10% by weight of the total composition of an electrolyte.
7. A detergent composition according to claim 6 characterized in that the electrolyte is sodium chloride.
8. A detergent composition according to any of the preceding claims, characterized in that it contains at least one ingredient which is in the form of solid particles.
9. A detergent composition according to any of the preceding claims, characterized in that it contains a peroxygen compound.
10. A detergent composition according to claims 8 and 9 characterized in that the peroxygen compound is in the form of particles having a diameter size in the range of from 1 micrometer to 350 micrometer.
11. A detergent composition according to claim 9 or 10 characterized in that the peroxygen compound is a perborate.
12. A detergent composition according to claim 9 or 10 characterized in that the peroxygen compound is a percarbonate.
13.
14.
15. 13. 14. 15. A detergent composition according to claims 8, 9 or 10 characterized in that it further comprises from 3% to 12% by weight of the total composition of ethanol. A detergent composition according to claims 9 to 13, which has a pH of at least 9. A detergent composition according to claim 1, substantially as hereinbefore described and exemplified.
IE424390A 1989-11-24 1990-11-23 Suspending liquid detergent compositions IE904243A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
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

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IE904243A1 true IE904243A1 (en) 1991-06-05

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EP (1) EP0430330A3 (en)
JP (1) JPH03210400A (en)
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)

Families Citing this family (11)

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Publication number Priority date Publication date Assignee Title
EP0482275B1 (en) * 1990-10-22 1996-07-10 The Procter & Gamble Company Stable liquid detergent compositions containing bleach
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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Publication number Priority date Publication date Assignee Title
JPS60168797A (en) * 1984-02-13 1985-09-02 花王株式会社 Abrasive-containing liquid detergent composition
GB8511303D0 (en) * 1985-05-03 1985-06-12 Procter & Gamble Liquid detergent compositions
GB8528521D0 (en) * 1985-11-20 1985-12-24 Procter & Gamble Liquid detergent compositions
DE3774312D1 (en) * 1986-03-31 1991-12-12 Procter & Gamble LIQUID CLEANING AGENT THAT CONTAINS ANIONIC SURFACE-ACTIVE SUBSTANCE, A SALT OF AMERICAN ACID AS A BUILD-UP AND A FATTY ACID.
GB8712430D0 (en) * 1987-05-27 1987-07-01 Procter & Gamble Liquid detergent
GB8713574D0 (en) * 1987-06-10 1987-07-15 Albright & Wilson Liquid detergent compositions
GB8713756D0 (en) * 1987-06-12 1987-07-15 Procter & Gamble Liquid detergent
ES2162785T3 (en) * 1989-02-27 2002-01-16 Unilever Nv LIQUID DETERGENT COMPOSITION.

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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
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
AU650247B2 (en) 1994-06-16

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