WO1993011216A1 - Rinse-active foam control particles - Google Patents

Rinse-active foam control particles Download PDF

Info

Publication number
WO1993011216A1
WO1993011216A1 PCT/US1992/010390 US9210390W WO9311216A1 WO 1993011216 A1 WO1993011216 A1 WO 1993011216A1 US 9210390 W US9210390 W US 9210390W WO 9311216 A1 WO9311216 A1 WO 9311216A1
Authority
WO
WIPO (PCT)
Prior art keywords
foam
soap
detergent composition
control particles
weight
Prior art date
Application number
PCT/US1992/010390
Other languages
French (fr)
Inventor
Alan David Brinson
David Xavante Cumming
David William York
Original Assignee
The Procter & Gamble Company
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
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to DE69230801T priority Critical patent/DE69230801T2/en
Priority to AT93900775T priority patent/ATE190644T1/en
Priority to JP51032493A priority patent/JP3357053B2/en
Priority to SK639-94A priority patent/SK63994A3/en
Priority to EP93900775A priority patent/EP0615540B1/en
Priority to BR9206856A priority patent/BR9206856A/en
Priority to US08/244,444 priority patent/US5591705A/en
Publication of WO1993011216A1 publication Critical patent/WO1993011216A1/en
Priority to FI942551A priority patent/FI942551A0/en
Priority to NO942053A priority patent/NO942053L/en

Links

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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0094High foaming 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
    • 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
    • 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
    • C11D13/00Making of soap or soap solutions in general; Apparatus therefor
    • C11D13/14Shaping
    • C11D13/20Shaping in the form of small particles, e.g. powder or flakes
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions

Definitions

  • the present invention is concerned with rinse-active foam control particles for inclusion in a detergent composition, i.e. foam control particles mainly active in the rinse-cycle of a laundry process, with a method for making such particles, and with detergent
  • compositions containing such particles are provided.
  • suds-control during the washing cycle of a laundry process is important, so as to avoid negative interference with the action of the wash liquor upon the fabrics, it is also known that suds-control during the rinse cycle of a laundry process is desirable; Indeed, excessive foaming during the rinse cycle in a washing machine can cause foam spillage and damage to the machine, while in a handwash context, there is an advantage in lowering the foam production during rinsing, so as to shorten this step.
  • Soaps of fatty acids have been used for such a rinse-active suds control function, and they have always been spray dried together with the rest of the detergent composition;
  • the present invention provides foam control fatty acid soap particles which are made separately from the rest of the spray-dried detergent composition, and a process to make them, not causing organic emissions.
  • the present invention provides rinse-active foam- control particles for inclusion in a detergent
  • composition in powder form consisting essentially of a soap of fatty acids of which at least 80% contain from 16 to 18 carbon atoms, the geometric mean
  • particle size of the particles being inferior to 1 mm, preferably inferior to 0.4 mm.
  • the present invention also encompasses a process for making said foam-control agents, as well as high suds and low sud executions of detergent compositions containing said foam-control particles.
  • the antifoam particles are the antifoam particles.
  • the foam-control particles of the invention are mainly constituted of a soap of fatty acids of which at least 80% by weight contain from 16 to 18 carbon atoms; preferred fatty acids are tallow or
  • tallow/coconut mixtures at a weight ratio of tallow to coconut not less than 70/30; particularly preferred is a 90/10 tallow/coconut mixture.
  • Suitable cations which render the soap water soluble and/or dispersible include sodium, potassium, ammonium,
  • the particles of the invention are further divided by the particles of the invention.
  • the geometric mean particle size which is the median of the cumulative weight distribution, should be less than 1 mm and preferably less than 0.4 mm.
  • the individual particle size of a particle is meant as being the sum of the longest and the shortest dimension of the particle divided by two.
  • the cumulative weight distribution of the particles can be conveniently measured by sieving with an airfluidized sieve.
  • the particles herein optionally include a free- flowing agent such as amorphous silica, at levels not exceeding 5% by weight of the particle.
  • the process herein contains essentially the steps of drying a fatty acid soap slurry to a low moisture level, i.e. a moisture level not exceeding 9%, preferably not exceeding 5% by weight of the slurry, then pressing the slurry into noodles, and
  • control of the moisture level is a particularly critical feature of the process herein, since
  • Drying of the soap slurry is preferably achieved under vacuum. Supplementary drying during the
  • grinding process may be appropriate, and achieved for example in an air classifier.
  • a typical method to measure the moisture level in the sopa slurry and/or the noodles is a solvent distillation method, using a Bidwell ® apparatus.
  • a detergent composition in powder form comprising a surface-active agent and foam control particles such as described above.
  • Addition of the particles herein in detergent compositions can be achieved by e.g. dry-mixing.
  • the amount of foam control particles is typically from 0.25 to 5% by weight of the composition, depending on the type of detergent composition involved.
  • a wide range of surfactants can be used in the detergent compositions.
  • anionic surfactants are particularly suitable herein, especially mixtures of sulphonate and sulphate surfactants in a weight ratio of from 5:1 to
  • Preferred sulphonates include alkyl benzene sulphonates having from 9 to 15, especially 11 to 13 carbon atoms in the alkyl radical, and alphasulphonated methyl fatty acid esters in which the fatty acid is derived from a C 12 -C 18 fatty source preferably from a C 16 -C 18 fatty source.
  • the cation is an alkali metal, preferably sodium.
  • Preferred sulphate surfactants are alkyl sulphates having from 12 to 18 carbon atoms in the alkyl radical , optionally in admixture with ethoxy sulphates having from 10 to 20, preferably 10 to 16 carbon atoms in the alkyl radical and an average degree of ethoxylation of 1 to 6.
  • alkyl sulphates herein are tallow alkyl sulphate, coconut alkyl sulphate, and C 14 -C 15 alkyl sulphates.
  • the cation in each instance is again an alkali metal cation, preferably sodium.
  • nonionic surfactants useful in the present invention are condensates of ethylene oxide with a hydrophobic moiety to provide a surfactant having an average hydrophilic-lipophilic balance (HLB) in the range from 8 to 17, preferably from 9.5 to 13.5, more preferably from 10 to 12.5.
  • HLB hydrophilic-lipophilic balance
  • (lipophilic) moiety may be aliphatic or aromatic in nature and the length of the polyoxyethylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
  • Especially preferred nonionic surfactants of this type are the C 9 -C 15 primary alcohol ethoxylates containing 3-8 moles of ethylene oxide per mole of alcohol, particularly the C 14 -C 15 primary alcohols containing 6-8 moles of ethylene oxide per mole of alcohol and the C 12 -C 14 primary alcohols containing 3-5 moles of ethylene oxide per mole o f alcohol.
  • Another class of nonionic surfactants comprises alkyl polyglucoside compounds of general formula
  • RO C n H 2n O
  • t Z x wherein Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; x is from 1.3 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides.
  • Compounds of this type and their use in detergent are disclosed in EP-B 0 070 077, 0 075 996 and 0 094 118.
  • nonionic surfactants are poly hydroxy fatty acid amide surfactants of the formula R 2
  • R 2 is C 5-31 hydrocarbyl
  • Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof.
  • R 1 is methyl
  • R 2 is a straight C 11 -C 15 alkyl or alkenyl chain such as coconut alkyl or mixtures thereof
  • Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction.
  • a further class of surfactants are the semi-polar surfactants such as amine oxides.
  • Suitable amine oxides are selected from mono C 8 -C 20 , preferably C 10 - C 14 N-alkyl or alkenyl amine oxides and propylene-1,3- diamine dioxides wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
  • Another class of surfactants are amphoteric and amphoteric
  • surfactants such as polyamine-based species.
  • Cationic surfactants can also be used in the
  • detergent compositions herein and suitable quaternary ammonium surfactants are selected from mono C 8 -C 16 , preferably C 10 -C 14 N-alkyl or alkenyl ammonium
  • the detergent compositions can comprise from 1%-70% by weight of surfactant, but usually the surfactant is present in the compositions herein an amount of from 1% to 30%, more preferably from 10-25% by weight.
  • the detergent compositions herein preferably also contain a builder, which can be selected from
  • phosphates aluminosilicate ion exchangers (zeolites), and water-soluble monomeric or oligomeric carboxylate chelating agents such as citrates, succinates,
  • Suitable builder materials include alkali metal carbonates, bicarbonates and silicates, organic phosphonates, amino polyalkylene phosphonates and amino polycarboxylates, ethylene diamine tetraacetic acid and nitrilotriacetic acid.
  • Other suitable water- soluble organic salts are the homo- or co-polymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms. Polymers of this type are disclosed in GB-A-1,596,756. Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70,000, especially about 40,000.
  • ingredients which typically form part of a detergent composition in powder form include filler salts such as sodium sulphates, bleaching agents, such as sodium perborate and percarbonate, bleach
  • carboxymethyl cellulase enzymes, such as proteases, amylases, lipases, and cellulases, brighteners, fabric softening clays, perfumes, dyes, pigments.
  • the detergent compositions herein can be of the "high-suds" type, and be designed for hand-wash or in upright washing machine utilization. In such
  • the level of foam control particles is typically from 2% to 5% by weight.
  • compositions of the invention can also be of the "low-suds” type and thus be adapted for use in washing machines of all types; in this latter category, detergent compositions encompass “compact” executions, where the density is typically above 550g/litre of composition, and the level of filler salt is typically below 5% by weight of the composition.
  • the level of foam-control particles is typically from 0.25% to 2%.
  • Such additional foam-control agents are preferably silicones.
  • TAS sodium salt of tallow alcohol sulfate
  • Nonionic fatty alcohol ( C14 - C15 ) ethoxylated with about 7 moles of ethylene oxide
  • Copolymer AA/MA copolymer of acrylic acid and maleic acid
  • Na Phosphonate sodium salt of ethylenediamine
  • TAED tetra acetyl ethylene diamine

Abstract

The present invention provides rinse-active foam-control particles for inclusion in a detergent composition in powder form, consisting essentially of a soap of fatty acids of which at least 80 % contain from 16 to 18 carbon atoms, the geometric mean particle size of the particles being inferior to 1 mm, preferably inferior to 0.4 mm. The present invention also encompasses a process for making said foam-control agents, as well as high sud and low sud executions of detergent compositions containing said foam-control particles.

Description

RINSE-ACTIVE FOAM CONTROL PARTICLES
Technical Field
The present invention is concerned with rinse-active foam control particles for inclusion in a detergent composition, i.e. foam control particles mainly active in the rinse-cycle of a laundry process, with a method for making such particles, and with detergent
compositions containing such particles.
Background
It has become common practice in the detergent industry to include in detergent compositions
materials which are intended to control the amount of foam produced during a laundry process.
Although suds-control during the washing cycle of a laundry process is important, so as to avoid negative interference with the action of the wash liquor upon the fabrics, it is also known that suds-control during the rinse cycle of a laundry process is desirable; Indeed, excessive foaming during the rinse cycle in a washing machine can cause foam spillage and damage to the machine, while in a handwash context, there is an advantage in lowering the foam production during rinsing, so as to shorten this step.
Soaps of fatty acids have been used for such a rinse-active suds control function, and they have always been spray dried together with the rest of the detergent composition;
However, there is a desire to reduce organic emissions during manufacturing of detergents, in particular during spray-drying.
The present invention provides foam control fatty acid soap particles which are made separately from the rest of the spray-dried detergent composition, and a process to make them, not causing organic emissions.
Summary of the Invention
The present invention provides rinse-active foam- control particles for inclusion in a detergent
composition in powder form, consisting essentially of a soap of fatty acids of which at least 80% contain from 16 to 18 carbon atoms, the geometric mean
particle size of the particles being inferior to 1 mm, preferably inferior to 0.4 mm.
The present invention also encompasses a process for making said foam-control agents, as well as high suds and low sud executions of detergent compositions containing said foam-control particles. Detailed Description of the Invention
The antifoam particles
The foam-control particles of the invention are mainly constituted of a soap of fatty acids of which at least 80% by weight contain from 16 to 18 carbon atoms; preferred fatty acids are tallow or
tallow/coconut mixtures at a weight ratio of tallow to coconut not less than 70/30; particularly preferred is a 90/10 tallow/coconut mixture. Suitable cations which render the soap water soluble and/or dispersible include sodium, potassium, ammonium,
monoethanolammonium, diethanolammonium,
triethanolammonium, tetramethylammonium, etc. Sodium ions are preferred.
The particles of the invention are further
characterized by their particle size, which is such that the geometric mean particle size, which is the median of the cumulative weight distribution, should be less than 1 mm and preferably less than 0.4 mm.
The individual particle size of a particle is meant as being the sum of the longest and the shortest dimension of the particle divided by two.
The cumulative weight distribution of the particles can be conveniently measured by sieving with an airfluidized sieve.
Optional Ingredients
The particles herein optionally include a free- flowing agent such as amorphous silica, at levels not exceeding 5% by weight of the particle. Making process for the anti-foam particles of the invention
The process herein contains essentially the steps of drying a fatty acid soap slurry to a low moisture level, i.e. a moisture level not exceeding 9%, preferably not exceeding 5% by weight of the slurry, then pressing the slurry into noodles, and
successively grinding the noodles to a fine powder with the particle size required herein.
The control of the moisture level is a particularly critical feature of the process herein, since
successful grinding to the required particle size will not be possible without meeting the claimed moisture level.
Drying of the soap slurry is preferably achieved under vacuum. Supplementary drying during the
grinding process may be appropriate, and achieved for example in an air classifier.
A typical method to measure the moisture level in the sopa slurry and/or the noodles is a solvent distillation method, using a Bidwell® apparatus.
Detergent composition
In another embodiment of the present invention, it is herewith provided a detergent composition in powder form, comprising a surface-active agent and foam control particles such as described above. Addition of the particles herein in detergent compositions can be achieved by e.g. dry-mixing. The amount of foam control particles is typically from 0.25 to 5% by weight of the composition, depending on the type of detergent composition involved. SURFACTANT
A wide range of surfactants can be used in the detergent compositions. A typical listing of anionic, nonionic, ampholytic and zwitterionic classes, and species of these surfactants, is given in US Patent 3,664,961 issued to Norris on May 23, 1972.
Mixtures of anionic surfactants are particularly suitable herein, especially mixtures of sulphonate and sulphate surfactants in a weight ratio of from 5:1 to
1:2, preferably from 3:1 to 2:3, more preferably from
3:1 to 1:1. Preferred sulphonates include alkyl benzene sulphonates having from 9 to 15, especially 11 to 13 carbon atoms in the alkyl radical, and alphasulphonated methyl fatty acid esters in which the fatty acid is derived from a C12-C18 fatty source preferably from a C16-C18 fatty source. In each instance the cation is an alkali metal, preferably sodium.
Preferred sulphate surfactants are alkyl sulphates having from 12 to 18 carbon atoms in the alkyl radical , optionally in admixture with ethoxy sulphates having from 10 to 20, preferably 10 to 16 carbon atoms in the alkyl radical and an average degree of ethoxylation of 1 to 6. Examples of preferred alkyl sulphates herein are tallow alkyl sulphate, coconut alkyl sulphate, and C14-C15alkyl sulphates. The cation in each instance is again an alkali metal cation, preferably sodium.
One class of nonionic surfactants useful in the present invention are condensates of ethylene oxide with a hydrophobic moiety to provide a surfactant having an average hydrophilic-lipophilic balance (HLB) in the range from 8 to 17, preferably from 9.5 to 13.5, more preferably from 10 to 12.5. The hydrophobic
(lipophilic) moiety may be aliphatic or aromatic in nature and the length of the polyoxyethylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements. Especially preferred nonionic surfactants of this type are the C9-C15 primary alcohol ethoxylates containing 3-8 moles of ethylene oxide per mole of alcohol, particularly the C14-C15 primary alcohols containing 6-8 moles of ethylene oxide per mole of alcohol and the C12-C14 primary alcohols containing 3-5 moles of ethylene oxide per mole o
Figure imgf000008_0003
f alcohol.
Figure imgf000008_0002
Another class of nonionic surfactants comprises alkyl polyglucoside compounds of general formula
RO (CnH2nO)tZx wherein Z is a moiety derived from glucose; R is a saturated hydrophobic alkyl group that contains from 12 to 18 carbon atoms; t is from 0 to 10 and n is 2 or 3; x is from 1.3 to 4, the compounds including less than 10% unreacted fatty alcohol and less than 50% short chain alkyl polyglucosides. Compounds of this type and their use in detergent are disclosed in EP-B 0 070 077, 0 075 996 and 0 094 118.
Also suitable as nonionic surfactants are poly hydroxy fatty acid amide surfactants of the formula R2
- C - - Z, wherein R1 is H,
Figure imgf000008_0001
R1
C1-4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl or a mixture thereof, R 2 is C5-31 hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof.
Preferably, R1 is methyl, R2 is a straight C11-C15alkyl or alkenyl chain such as coconut alkyl or mixtures thereof, and Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction.
A further class of surfactants are the semi-polar surfactants such as amine oxides. Suitable amine oxides are selected from mono C8-C20, preferably C10- C14 N-alkyl or alkenyl amine oxides and propylene-1,3- diamine dioxides wherein the remaining N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
Another class of surfactants are amphoteric
surfactants, such as polyamine-based species.
Cationic surfactants can also be used in the
detergent compositions herein and suitable quaternary ammonium surfactants are selected from mono C8-C16 , preferably C10-C14 N-alkyl or alkenyl ammonium
surfactants wherein remaining N positions are
substituted by methyl, hydroxyethyl or hydroxypropyl groups.
Mixtures of surfactant types are preferred, more especially anionic-nonionic and also anionic-nonionic- cationic mixtures. Particularly preferred mixtures are described in British Patent No. 2040987 and European Published Application No. 0 087 914. The detergent compositions can comprise from 1%-70% by weight of surfactant, but usually the surfactant is present in the compositions herein an amount of from 1% to 30%, more preferably from 10-25% by weight.
The detergent compositions herein preferably also contain a builder, which can be selected from
phosphates, aluminosilicate ion exchangers (zeolites), and water-soluble monomeric or oligomeric carboxylate chelating agents such as citrates, succinates,
oxydisuccinates, as well as mixtures of the above species.
Other suitable builder materials include alkali metal carbonates, bicarbonates and silicates, organic phosphonates, amino polyalkylene phosphonates and amino polycarboxylates, ethylene diamine tetraacetic acid and nitrilotriacetic acid. Other suitable water- soluble organic salts are the homo- or co-polymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms. Polymers of this type are disclosed in GB-A-1,596,756. Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70,000, especially about 40,000.
Other ingredients which typically form part of a detergent composition in powder form include filler salts such as sodium sulphates, bleaching agents, such as sodium perborate and percarbonate, bleach
activators, anti redeposition agents such as
carboxymethyl cellulase, enzymes, such as proteases, amylases, lipases, and cellulases, brighteners, fabric softening clays, perfumes, dyes, pigments.
The detergent compositions herein can be of the "high-suds" type, and be designed for hand-wash or in upright washing machine utilization. In such
executions, the level of foam control particles is typically from 2% to 5% by weight.
The compositions of the invention can also be of the "low-suds" type and thus be adapted for use in washing machines of all types; in this latter category, detergent compositions encompass "compact" executions, where the density is typically above 550g/litre of composition, and the level of filler salt is typically below 5% by weight of the composition.
In such executions, the level of foam-control particles is typically from 0.25% to 2%.
In the "low-suds" execution herein, a sudscontrolling agent active in the wash cycle is
typically included, in addition to the rinse-active foam-control agents of the invention. Such additional foam-control agents are preferably silicones.
EXAMPLES
The following examples illustrate the invention and facilitate its understanding.
The abbreviations for the individual ingredients have the following meaning :
LAS: sodium salt of linear dodecyl benzene sulfonate
TAS: sodium salt of tallow alcohol sulfate
Nonionic: fatty alcohol ( C14 - C15 ) ethoxylated with about 7 moles of ethylene oxide
Copolymer AA/MA: copolymer of acrylic acid and maleic acid
CMC: carboxymethylcellulose
Na Phosphonate: sodium salt of ethylenediamine
tetramethylene phosphonic acid
TAED: tetra acetyl ethylene diamine
The following compositions were prepared.
Example I ("High Suds" execution)
LAS 20%
Sodium Tripolyphosphate 23%
Sodium Silicate 6%
CMC 0.15%
Sodium Sulphate 34%
Na Phosphonate 0.1%
Sodium Carbonate 5%
Copolymer AA/MA 2.5%
Sodium Soap *particles* 3%
Enzyme, brighteners, perfume and
minors up to 100
Density 360g/l
* prepared as described above and dry-mixed with the rest of the composition. Example II ( "Low Suds" execution, in compact form)
LAS 8%
TAS 2%
Nonionic 6%
Sodium Carbonate 14%
Sodium Citrate 6%
Zeolite 20%
Sodium Silicate 3%
CMC 0.5%
Sodium Sulphate 3.5%
Na Phosphonate 0.4%
Sodium Na Perborate Monohydrate 16%
Sodium Soap *particles* 1%
Silicone 0.5%
Sodium Salt of Copolymer AA/MA 4%
TAED 5%
Enzyme, perfume, brighteners and
minors up to 100
Density 700g/l
* prepared as described above and dry-mixed with the rest of the composition.

Claims

1. Rinse active foam-control particles for inclusion in a detergent composition in powder form, consisting essentially of a soap of fatty acids of which at least 80% contain from 16 to 18 carbon atoms, the geometric mean particle size of the particles being inferior to 1 mm.
2. Foam-control particles according to claim 1 having a geometric mean particle size inferior to 0.4 mm.
3. Foam-control particles according to claim 1 wherein the soap of fatty acids is selected from tallow soap, and tallow/coconut soap with a weight ratio of tallow to coconut not less than 70/30.
4. A process for making a foam-control agent
according to claims 1-3, wherein a fatty acid soap slurry is dried to a moisture level inferior to 9% by weight of the slurry, pressed into noodles, and the noodles are ground to a fine powder.
5. A process according to claim 4 wherein the soap slurry is dried to a moisture level not exceeding 5% by weight of the slurry.
6. A process according to claim 4 wherein the soap slurry is vacuum dried.
7. A high-suds detergent composition in powder form comprising a surface-active agent, and from 2 to 5% by weight foam-control particles according to any of claims 1-3.
8. A low suds detergent composition in powder form comprising a surface-active agent, and from 0.25 to 2% by weight foam-control particles according to any of claims 1-3.
9. A detergent composition according to claim 8 which also contains a silicone foam-control agent active in the wash cycle.
10. A detergent composition according to claims 7-8 which also contains a builder selected from the group of phosphates, phosphonates, aluminosilicate ion exchangers, citrates, carbonates, silicates, and mixtures thereof.
PCT/US1992/010390 1991-12-03 1992-12-01 Rinse-active foam control particles WO1993011216A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
DE69230801T DE69230801T2 (en) 1991-12-03 1992-12-01 METHOD FOR THE PRODUCTION OF FLUSH-ACTIVE FOAM-BRAKING PARTICLES
AT93900775T ATE190644T1 (en) 1991-12-03 1992-12-01 METHOD FOR PRODUCING RINSING-ACTIVE FOAM-BREAKING PARTICLES
JP51032493A JP3357053B2 (en) 1991-12-03 1992-12-01 Rinse activated foam control particles
SK639-94A SK63994A3 (en) 1991-12-03 1992-12-01 Rinse-active foam control particles
EP93900775A EP0615540B1 (en) 1991-12-03 1992-12-01 Process for making rinse-active foam control particles
BR9206856A BR9206856A (en) 1991-12-03 1992-12-01 Active foaming control particles in rinse
US08/244,444 US5591705A (en) 1991-12-03 1992-12-01 Rinse-active foam control particles
FI942551A FI942551A0 (en) 1991-12-03 1994-05-31 Active antifoam particles during rinsing
NO942053A NO942053L (en) 1991-12-03 1994-06-02 Rinse-active, foam-regulating particles

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP91203149.9 1991-12-03
EP91203149A EP0544944A1 (en) 1991-12-03 1991-12-03 Rinse-active foam control particles

Publications (1)

Publication Number Publication Date
WO1993011216A1 true WO1993011216A1 (en) 1993-06-10

Family

ID=8208047

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1992/010390 WO1993011216A1 (en) 1991-12-03 1992-12-01 Rinse-active foam control particles

Country Status (20)

Country Link
EP (2) EP0544944A1 (en)
JP (1) JP3357053B2 (en)
CN (1) CN1040022C (en)
AT (1) ATE190644T1 (en)
AU (1) AU3234193A (en)
BR (1) BR9206856A (en)
CA (1) CA2124790C (en)
CZ (1) CZ123294A3 (en)
DE (1) DE69230801T2 (en)
EG (1) EG20160A (en)
ES (1) ES2142859T3 (en)
FI (1) FI942551A0 (en)
HU (1) HUT67495A (en)
MA (1) MA22726A1 (en)
MX (1) MX9206959A (en)
NO (1) NO942053L (en)
PH (1) PH31575A (en)
SK (1) SK63994A3 (en)
TR (1) TR27153A (en)
WO (1) WO1993011216A1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4310672A1 (en) * 1993-04-01 1994-10-06 Henkel Kgaa Production of free-flowing detergents
US5972869A (en) * 1996-12-17 1999-10-26 Colgate-Palmolive Co Mildly acidic laundry detergent composition providing improved protection of fine fabrics during washing and enhanced rinsing in hand wash
US6150324A (en) * 1997-01-13 2000-11-21 Ecolab, Inc. Alkaline detergent containing mixed organic and inorganic sequestrants resulting in improved soil removal
US6773625B2 (en) * 2002-08-26 2004-08-10 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Dry bleach compositions
WO2004053039A2 (en) * 2002-12-11 2004-06-24 Novozymes A/S Detergent composition comprising endo-glucanase
CN114644961A (en) * 2014-08-01 2022-06-21 宝洁公司 Cleansing compositions comprising high fatty acids
WO2017093023A1 (en) * 2015-12-02 2017-06-08 Unilever N.V. Hard surface cleaning composition
CN111201310B (en) * 2017-10-19 2021-08-06 宝洁公司 Cleaning compositions comprising fatty acid blends

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1489395A (en) * 1965-08-20 1967-07-21 Henkel & Cie Gmbh Low foaming detergents
GB1204123A (en) * 1966-11-29 1970-09-03 Unilever Ltd Detergent composition
US4192761A (en) * 1977-06-23 1980-03-11 The Procter & Gamble Company Detergent compositions containing a suds regulating system
US4321165A (en) * 1977-06-29 1982-03-23 The Procter & Gamble Company Detergent compositions comprising cationic, anionic and nonionic surfactants
US4338204A (en) * 1979-09-29 1982-07-06 The Procter & Gamble Company Detergent softener containing anionic, amine, and water soluble cationic
US4347168A (en) * 1977-11-17 1982-08-31 The Procter & Gamble Company Spray-dried granular detergent compositions for improved greasy soil removal
US4391726A (en) * 1980-11-28 1983-07-05 The Procter & Gamble Company Detergent composition containing low levels of amine oxides
US4430243A (en) * 1981-08-08 1984-02-07 The Procter & Gamble Company Bleach catalyst compositions and use thereof in laundry bleaching and detergent compositions
US4687592A (en) * 1985-02-19 1987-08-18 The Procter & Gamble Company Detergency builder system

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB486819A (en) * 1936-06-18 1938-06-10 Lever Brothers Ltd Improvements in soap products and in the manufacture thereof
GB1237084A (en) * 1967-10-02 1971-06-30 Unilever Ltd Soap drying process
DE2327141C3 (en) * 1973-05-28 1978-10-05 Hoechst Ag, 6000 Frankfurt Builders for detergents and cleaning agents
GR68037B (en) * 1979-03-15 1981-10-27 Procter & Gamble
GB8518871D0 (en) * 1985-07-25 1985-08-29 Dow Corning Ltd Detergent foam control agents
GB8625474D0 (en) * 1986-10-24 1986-11-26 Unilever Plc Soap noodles
DE3834181A1 (en) * 1988-10-07 1990-04-12 Henkel Kgaa LIQUID DETERGENT
IT1236128B (en) * 1989-11-15 1993-01-08 Mira Lanza Spa POWDER DETERGENT, WITH HIGH CONTENT OF NONIONIC SURFACTANTS AND SOAPS.

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1489395A (en) * 1965-08-20 1967-07-21 Henkel & Cie Gmbh Low foaming detergents
GB1204123A (en) * 1966-11-29 1970-09-03 Unilever Ltd Detergent composition
US4192761A (en) * 1977-06-23 1980-03-11 The Procter & Gamble Company Detergent compositions containing a suds regulating system
US4321165A (en) * 1977-06-29 1982-03-23 The Procter & Gamble Company Detergent compositions comprising cationic, anionic and nonionic surfactants
US4347168A (en) * 1977-11-17 1982-08-31 The Procter & Gamble Company Spray-dried granular detergent compositions for improved greasy soil removal
US4338204A (en) * 1979-09-29 1982-07-06 The Procter & Gamble Company Detergent softener containing anionic, amine, and water soluble cationic
US4391726A (en) * 1980-11-28 1983-07-05 The Procter & Gamble Company Detergent composition containing low levels of amine oxides
US4430243A (en) * 1981-08-08 1984-02-07 The Procter & Gamble Company Bleach catalyst compositions and use thereof in laundry bleaching and detergent compositions
US4687592A (en) * 1985-02-19 1987-08-18 The Procter & Gamble Company Detergency builder system

Also Published As

Publication number Publication date
PH31575A (en) 1998-11-03
CN1040022C (en) 1998-09-30
DE69230801D1 (en) 2000-04-20
AU3234193A (en) 1993-06-28
JP3357053B2 (en) 2002-12-16
FI942551A (en) 1994-05-31
EP0615540A1 (en) 1994-09-21
MA22726A1 (en) 1993-07-01
NO942053D0 (en) 1994-06-02
TR27153A (en) 1994-11-09
CZ123294A3 (en) 1995-02-15
HUT67495A (en) 1995-04-28
ATE190644T1 (en) 2000-04-15
MX9206959A (en) 1993-06-30
CA2124790C (en) 1998-06-30
ES2142859T3 (en) 2000-05-01
SK63994A3 (en) 1994-10-05
FI942551A0 (en) 1994-05-31
CA2124790A1 (en) 1993-06-10
EP0544944A1 (en) 1993-06-09
NO942053L (en) 1994-06-02
JPH07501575A (en) 1995-02-16
EG20160A (en) 1997-08-31
HU9401356D0 (en) 1994-08-29
EP0615540A4 (en) 1994-09-28
EP0615540B1 (en) 2000-03-15
CN1075507A (en) 1993-08-25
BR9206856A (en) 1995-05-02
DE69230801T2 (en) 2000-11-02

Similar Documents

Publication Publication Date Title
EP0358474B1 (en) Detergent compositions
AU616204B2 (en) A composition for softening fabrics
US4758378A (en) Softening detergent compositions containing amide softening agent
WO1992013054A1 (en) Detergent compositions containing lipase and water-soluble quaternary ammonium compounds
IE61938B1 (en) Detergent compositions
AU624577B2 (en) Detergent compositions
JPH0516480B2 (en)
US4885101A (en) Laundry detergents containing fabric-softening clays between 150 and 2000 microns in size
EP0163352B1 (en) Detergent with suds control
GB2172910A (en) Detergent or sheet containing a fabric conditioner
EP0615540B1 (en) Process for making rinse-active foam control particles
EP0358473B2 (en) Detergent compositions
EP0287344B1 (en) Use of a composition for softening fabrics
US5591705A (en) Rinse-active foam control particles
EP0358472B1 (en) Detergent compositions
US20110241235A1 (en) Process for preparing spray-dried particles
US20050187127A1 (en) Laundry detergent composition comprising an anionic detersive surfactant, sulphamic acid and/or water soluble salts thereof, and a sulphate salt
IE60065B1 (en) Softening and bleaching detergent compositions containing amide softening agent
EP0286342B1 (en) Light duty detergent powder composition
EP0488750B1 (en) Process and composition for treating fabrics

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU BB BG BR CA CS FI HU JP KP KR LK MG MN MW NO NZ PL RO RU SD UA US

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 1993900775

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: PV1994-1232

Country of ref document: CZ

WWE Wipo information: entry into national phase

Ref document number: 63994

Country of ref document: SK

WWE Wipo information: entry into national phase

Ref document number: 2124790

Country of ref document: CA

Ref document number: 942551

Country of ref document: FI

WWP Wipo information: published in national office

Ref document number: 1993900775

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 08244444

Country of ref document: US

WWP Wipo information: published in national office

Ref document number: PV1994-1232

Country of ref document: CZ

WWR Wipo information: refused in national office

Ref document number: PV1994-1232

Country of ref document: CZ

WWG Wipo information: grant in national office

Ref document number: 1993900775

Country of ref document: EP