EP1115825A1 - Compositions detergentes solides - Google Patents

Compositions detergentes solides

Info

Publication number
EP1115825A1
EP1115825A1 EP98948562A EP98948562A EP1115825A1 EP 1115825 A1 EP1115825 A1 EP 1115825A1 EP 98948562 A EP98948562 A EP 98948562A EP 98948562 A EP98948562 A EP 98948562A EP 1115825 A1 EP1115825 A1 EP 1115825A1
Authority
EP
European Patent Office
Prior art keywords
weight
builder
water
surfactant
acid
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP98948562A
Other languages
German (de)
English (en)
Inventor
Richard Timothy Hartshorn
Zayeed Alam
Sylvestre Canceil
Alan Thomas Brooker
Kevin Norwood
David Scott Bohlen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
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 Procter and Gamble Co filed Critical Procter and Gamble Co
Publication of EP1115825A1 publication Critical patent/EP1115825A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/37—Mixtures of compounds all of which are anionic
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047—Detergents in the form of bars or tablets
    • C11D17/0065—Solid detergents containing builders
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0052—Gas evolving or heat producing compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
    • C11D3/1273—Crystalline layered silicates of type NaMeSixO2x+1YH2O
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/12—Water-insoluble compounds
    • C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246—Silicates, e.g. diatomaceous earth
    • C11D3/128—Aluminium silicates, e.g. zeolites
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2082—Polycarboxylic acids-salts thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/20—Organic compounds containing oxygen
    • C11D3/2075—Carboxylic acids-salts thereof
    • C11D3/2086—Hydroxy carboxylic acids-salts thereof
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/26—Organic compounds containing nitrogen
    • C11D3/33—Amino carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/36—Organic compounds containing phosphorus
    • C11D3/361—Phosphonates, phosphinates or phosphonites
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
    • C11D3/3761—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions in solid compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02—Anionic compounds
    • C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29—Sulfates of polyoxyalkylene ethers

Definitions

  • the invention relates to solid detergent compositions comprising improved builder systems and surfactant systems which have an improved delivery to the wash and an improved cleaning performance.
  • Detergent manufacturers spend much time and effort on further improving their products to meet consumer needs, for example by improving the performance of the products, the easy of handling of the products, or the delivery of the product to the wash.
  • surfactants and builders are essential to provide building of the washing liquor, by binding, complexing or dispersing the hard water ions which interfere with various ingredients but in particular with the surfactants present in the detergents, which reduces their performance, for example their surfactancy, which is of course undesirable.
  • certain builders can bind or complex certain heavy metal ions present in the washing process or in the detergent or introduced in the detergent during the making process, which can interfere with detergent ingredients such as oxygen bleach, both during the wash and during storage.
  • the most commonly used builders present in about all commercially available detergents which do not contain phosphate builders, are aluminosilicates. They are inexpensive builders which have as an additional benefit that they are easy to process. In fact they are useful process aids because they are very good binders or carrier material for other detergent ingredients. Furthermore, they are useful as dusting agent, to reduce the stickiness or caking of the product.
  • aluminosilicate builders are combined with other builder materials.
  • EP-A-554287 describes builder systems comprising high levels of zeolite A, layered silicates and polymeric compounds.
  • WO 97/17045 described builders systems with reduced levels of zeolite A, replaced with higher levels of amorphous silicates and carbonates.
  • the inventors have found that most detergent compositions leave residues in the washing machine and on the fabrics, which are difficult to remove. They have also found that these residues can become entrapped in the fibres of the fabric, which makes it even more difficult to remove the residues.
  • the inventors have found that the one of the main reasons for this problem is the presence of in particular powdered, insoluble builders, including aluminosilicates and amorphous silicates.
  • the inventors have now found that an improved phosphate-free detergent composition is obtained when a specific builder system, preferably combined with specific surfactant system are used, preferably incorporated in the composition in the form of a specific particular component.
  • a specific builder system preferably combined with specific surfactant system are used, preferably incorporated in the composition in the form of a specific particular component.
  • compositions herein have a surprisingly improved delivery to the wash. They have a reduced gelling upon contact with water, improved dispensing and a reduced residue formation. A fast and efficient building of the washing liquor is achieved, whereby a very effective cleaning performance is obtained.
  • the delivery to the wash of the product may be further improved when a water soluble polymeric polycarboxylic acid or salt is present, and optionally further polymeric flocculating polymer is present, in particular combined with an monomeric (poly) carboxylate or more preferably the acid form thereof.
  • These detergent compositions may comprise particles which are free of sprayed-on nonionic alkoxylated alcohol surfactants. This may help to reduce the gelling and caking of the products.
  • a further advantage can be that the omission of sprayed-on nonionic alkoxylated alcohols allows the reduction or omission of powdered materials such as fine aluminosilicate material and amorphous silicate material, which are normally used to dust the detergent particles containing these sprayed-on nonionic surfactants, to reduce caking. This also allows a reduction of the process complexity.
  • the invention provides a phosphate-free detergent composition comprising at least one particulate components, from 5% to 90% by weight of the composition of a builder system and at least 10% by weight of the composition of a surfactant system, comprising one or more surfactants, characterised in that
  • the builder system comprises at least two builders selected from water-soluble or partially water-soluble builders or mixtures thereof, present at a level from 60% to 100% by weight of the builder system; and from 0% to 40% by weight of the builder system of water-insoluble builders, provided that less than 9% by weight of the composition of aluminosilicate builder is present, and less than 5% by weight of the composition of amorphous sodium silicate is present; and
  • the particulate component comprises at least one of the surfactants of the surfactant system is intimately mixed with at least one of the water-soluble or partially water- soluble builders. It has been found that theses detergent compositions have a reduced gelling upon contact with water, an improved dispensing and a reduced residue formation, whereby a very good building of the wash water and a very good cleaning performance is achieved.
  • the detergent composition preferably a builder system which comprises less than 30% or even less than 20% or even less than 10% by weight of water insoluble builder, whereby in the preferred embodiments the balance of the builder system are the water-soluble builders and/ or partially water soluble builders.
  • aluminosilicate preferably less than 6% or even less than 4% or even less than 2% by weight of the composition.
  • the aluminosilicate may be contained in a component containing other detergent ingredients, such as in a detergent agglomerate, extrudate or a blown powder. It may even be preferred that substantially no aluminosilicate is present as separate particulate ingredient.
  • amorphous silicate is present.
  • the amorphous silicate is preferably contained in a component containing other detergent ingredients, such as in a detergent agglomerate, extrudate or a blown powder. It may be preferred that substantially no amorphous silicate is present as separate particulate ingredient.
  • the water-soluble builder and partially water-soluble builder are typically present at a level up to 50% by weight, preferably up to 35% by weight, most preferably from 3% to 30% by weight of the composition, or even from 6% to 30% or even from 8% to 25%.
  • the detergent composition of the invention comprises at least one particulate component containing an intimate mixture of one or more of the water soluble or partially water soluble builders and one or more surfactants. It may be preferred that the component comprises more than one of these builders.
  • At least two particulate components are present in the detergent composition, which comprise intimate mixtures of a surfactants and a water-soluble builder.
  • Such intimate mixtures can be obtained by any process involving the mixing of the components, which can be part of a granulation processes including a spray-drying process, an extrusion process and an agglomeration processes and also a tableting process.
  • a first step comprises forming of a mixture of the surfactant and the water soluble or partially water soluble builder, and granulation of the mixture to form a particular component, preferably a granule.
  • the intimately mixing preferably results in an agglomerate or a spray-dried or blown powder, an extrudate .
  • the particulate components herein preferably has a particle size of at least 50 microns, preferably they have an weight average particle size of more than 150 or more than 250 microns or even more than 350 microns, as measured by sieving the composition on sieves of different mesh size, and calculating the fraction which remain on the sieve and the fraction which passes through the sieve.
  • the density of the component is from 250 g/litre to 1500 g/litre, more preferably at least one of the components, preferably all of the components, has a density from 400 g/litre to 1200gr/litre, more preferably from 500 g/litre to 900g/litre.
  • Preferred components comprise an intimate mixture of at least one anionic surfactant and one or more of the water-soluble or partially water soluble builders.
  • a partially water-soluble builder When a partially water-soluble builder is present, it may be preferred that at least 50% thereof or even substantially all of the partially water-insoluble builder is present in a component herein, preferably in an intimate mixture with one or more anionic surfactants.
  • a highly preferred additional ingredient of the detergent compositions herein may be oxygen based bleach, preferably containing an hydrogen peroxide source, preferably a perhydrogen compound and a bleach activator, described herein after. It has been found that the improved product delivery to the wash results in an improved delivery of the bleach system therein, which reduces the risk of deposition of bleach on the fabric and the risk of patchy fabric damage.
  • the compositions herein comprise a component which contains high levels of an alkyl sulfate or sulphonate surfactant or mixtures thereof, preferably an alkyl benzene sulphonate, intimately mixed with an sulphate salt and moisture.
  • a component comprising from 85% to 95% of one an anionic sulfate or sulphonate surfactant and from 15% to 5% sulfate salt and moisture.
  • a component may be in the form f a flake, which can be admixed or dry-added to the other components of the detergent composition herein.
  • the components of the compositors herein are free of sprayed-on nonionic alkoxylated alcohol surfactants. It has been found that hereby the delivery of the composition to the washing water can be improved and the caking of the product can be reduced. It may be preferred that the composition comprises a nonionic surfactant which is solid at temperatures below 30°C or even 40°C, preferably present in an intimate mixture with other ingredients.
  • compositions thereof comprises a perfume, brightener or dye or mixtures thereof, which may be sprayed onto the particular component herein.
  • compositions may contain an effervescence system to further improve the delivery of the detergent composition to the washing water.
  • Water-Soluble or Partially Water-Soluble Builders are partially Water-Soluble Builders
  • the composition comprises two or more water-soluble or partially water soluble builders or mixtures thereof. These include crystalline layered silicates an organic carboxylates or carboxylic acids.
  • the preferred crystalline layered silicate herein have the general formula
  • M is sodium or hydrogen
  • x is a number from 1.9 to 4 and y is a number from 0 to 20.
  • Crystalline layered sodium silicates of this type are disclosed in EP-A-0164514 and methods for their preparation are disclosed in DE-A-3417649 and DE-A-3742043.
  • x in the general formula above has a value of 2, 3 or 4 and is preferably 2.
  • M is preferably H, K or Na or mixtures thereof, preferably Na.
  • the most preferred material is ⁇ -Na2Si2 ⁇ 5 5 R. Na2S ⁇ 2 ⁇ 5 or ⁇ -Na2Si2 ⁇ 5, or mixtures thereof, preferably being at least 75% -Na2Si2 ⁇ 5 for example available from Clariant as
  • the crystalline layered silicate material in particular of the formula Na2Si2 ⁇ 5 may optionally comprise other elements such as B, P, S, for example obtained by processes as described in EP 578986-B.
  • the partially water-soluble builder is preferably present at a level up to 40%, more preferably up to 35%.
  • the composition of the invention comprises from 10% to 40%, more preferably from 12% to 35% or even from 15% to 25%o by weight of the composition of the partially water-soluble builder.
  • crystalline layered silicate when present, part of or all of this is in an intimate mixture with a surfactant, preferably an anionic surfactant.
  • a preferred particulate component herein may comprise an intimate mixture of preferably from 25% to 75% by weight, more preferably from 35%) to 68%, even more preferably from 45% to 62%> by weight of the component of a of a crystalline layered silicate and from 25% to 75% by weight, more preferably from 32% to 62% by weight more preferably from 38% to 48% by weight of the component of an anionic surfactant.
  • Such a particulate component preferably comprises less than 10% by weight of free moisture, preferably less than 5%, or even less than 3% or even less than 2% by weight.
  • the free moisture content as used herein can be determined by placing 5 grams of the particulate component in a petri dish and placing this petri dish in a convection oven at 50°C for 2 hours, and subsequently measuring the weight loss, due to water evaporation
  • the anionic surfactant comprises from 50% to 100% by weight, preferably from 60% or even 75% to 100% of the anionic surfactant of a sulphonate surfactant preferably an alkyl benzene sulphonate surfactant, as described herein.
  • the weight ratio of the crystalline layered silicate to the anionic surfactant in the intimate mixture is from 4:5 to 7:3, more preferably from 1 : 1 to 2:1, most preferably from 5:4 to 3:2.
  • Such a component may be prepared by any method, preferably by roller compaction or more preferably by agglomeration, as known in the art.
  • Such component may also comprise additional ingredients, for example in amounts of from 0% to 25%, generally no greater than 20% or even 15%) by weight of the agglomerate.
  • additional ingredients for example in amounts of from 0% to 25%, generally no greater than 20% or even 15%.
  • levels of incorporation thereof will depend on the application of the component or compositions and the physical form of the components and the compositions.
  • the crystalline layered silicate may also be in an intimate mixture with other materials, including one or more of the water-soluble builders or polymeric compounds such as acrylic and/ or maleic acid polymers, inorganic acids or salts, including carbonates and sulphates, or small levels of other silicate material, including amorphous silicate, meta silicates, and aluminosilicates, as described herein.
  • water-soluble builders or polymeric compounds such as acrylic and/ or maleic acid polymers, inorganic acids or salts, including carbonates and sulphates, or small levels of other silicate material, including amorphous silicate, meta silicates, and aluminosilicates, as described herein.
  • the water soluble builders include organic carboxylic acids and salts thereof.
  • Suitable water-soluble builder compounds include the water soluble monomeric polycarboxylates, or their acid forms, homo or copolymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxylic radicals separated from each other by not more that two carbon atoms and mixtures of any of the foregoing.
  • the carboxylate or polycarboxylate builder can be momomeric or oligomeric in type although monomeric polycarboxylates are generally preferred for reasons of cost and performance.
  • polymeric polycarboxylates may be present, including homo and copolymers of maleic acid and acrylic acid and their salts.
  • Suitable carboxylates containing one carboxy group include the water soluble salts of lactic acid, glycolic acid and ether derivatives thereof.
  • Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycolic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates and the sulfinyl carboxylates.
  • Polycarboxylates containing three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No.
  • Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in British Patent No. 1,261,829, 1,1,2,2-ethane tetracarboxylates, 1,1, 3, 3 -propane tetracarboxylates and 1,1,2,3-propane tetracarboxylates.
  • Polycarboxylates containing sulfo substituents include the sulfosuccinate derivatives disclosed in British Patent Nos. 1,398,421 and 1,398,422 and in U.S. Patent No. 3,936,448, and the sulfonated pyrolysed citrates described in British Patent No. 1,439,000.
  • Preferred polycarboxylates are hydroxycarboxylates containing up to three carboxy groups per molecule, more particularly citrates.
  • the parent acids of the monomeric or oligomeric polycarboxylate chelating agents or mixtures thereof with their salts, e.g. citric acid or citrate/citric acid mixtures, are also contemplated as useful builder components.
  • acetic acid citric acid, malic acid, and fumaric acid, or their salts or mixtures thereof. It may be preferred that mixtures of the salt and acid form are present.
  • the water soluble builder is preferably present at a level up to 40%, more preferably up to 35%).
  • the composition of the invention comprises from 10%) to 40%, more preferably from 12% to 35% or even from 15% to 25% by weight of the composition of the water-soluble builder.
  • part or even all of the monomeric or oligomeric (poly)carboxylic acid or salt thereof is in the form of a separate particle, whereby it may be preferred that the average particle size of this builder material is then preferably less than 150 microns, or even less than 100 microns.
  • part of the water-soluble or partially water-soluble builder is used as dusting agent, to reduce the caking of the product when necessary.
  • Suitable water-soluble builder materials are polymeric polycarboxylic acids or polycarboxylates, including the water soluble 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 the latter type are disclosed in GB-A-1, 596,756.
  • Examples of such salts are polyacrylates of MWt 1000-50000, preferably 10000 or even 7000 and copolymers of (poly)acrylate and maleic acid or anhydride, such copolymers having preferably a molecular weight of from 2000 to 100,000, especially 40,000 to 80,000.
  • a polycarboxylate polymer such as polymer and copolymer of maleic anhydride or acid and (poly)acrylic acid and their salts, is incorporated at a level of from 0.5% to 15%, preferably from 1% to 12% or even from 2% to 8% by weight of the composition.
  • the water-insoluble builder and the polymer are not in an intimate mixture with one another.
  • the inventors have also found that when a polymeric polycarboxylate is present, it may be preferred that the polymer is comprised in an intimate mixture, preferably a spray- dried particle, which is prepared by first mixing a carbonate salt and the polymer and then addition and intimately mixing of other ingredients.
  • an intimate mixture preferably a spray- dried particle, which is prepared by first mixing a carbonate salt and the polymer and then addition and intimately mixing of other ingredients.
  • the degree of mixing between amorphous silicate and an anionic surfactant is reduced, when an amorphous silicate is present, in particular in mixtures containing anionic surfactant which are to be spray-dried, it may be beneficial to reduce the amount of silicate present, for example to levels of less than 3% by weight of the mixture, or even less than 2%, or even less thanl% or even 0% by weight of the mixture.
  • the surfactant system preferably comprises at least one type of anionic surfactant and two or more anionic surfactants are preferably present.
  • Fatty acid soaps may be present, also to control the sudsing in the wash.
  • anionic surfactant when only anionic surfactant is present, it may be preferred that this is comprised in more than one particulate, intimately mixed component of the composition herein.
  • the surfactant system also comprise cationic and it may be preferred that these or part thereof are intimately mixed with an anionic surfactant.
  • the surfactant system may also comprise nonionic surfactants and it may also be preferred that part or all of the nonionic surfactant is in an intimate mixture with the anionic surfactants.
  • the surfactant system is substantially free of linear alkyl sulfate surfactant.
  • at least an anionic sulphonate surfactant is present, preferably comprised in at least two particulate components, preferably at least at a level of 10% by weight of the composition, more preferably at least 12% or even 15% by weight.
  • a mid-chain branched alkyl sulfate surfactant whereby it may be preferred that only limited levels of sulphonate surfactant are present, for example less than 10% or even less than 8% or even form 0% to 5% by weight of the composition.
  • ampholytic, amphoteric and zwitteronic surfactants are generally used in combination with anionic and/or nonionic surfactants.
  • the anionic surfactant herein preferably comprises at least a sulphate surfactant and/ or a sulphonate surfactant or mixtures thereof.
  • compositions herein comprise a particulate component, preferably in the form of a flake of an alkyl sulfate or sulphonate surfactant, preferably an alkyl benzene sulphonate, present at a concentration of from 85% to 95% of the particle or flake, the balance being an sulfate salt and moisture, the particle or flake being admixed to the other detergent component(s) or ingredients.
  • a particulate component preferably in the form of a flake of an alkyl sulfate or sulphonate surfactant, preferably an alkyl benzene sulphonate, present at a concentration of from 85% to 95% of the particle or flake, the balance being an sulfate salt and moisture, the particle or flake being admixed to the other detergent component(s) or ingredients.
  • anionic surfactants include the isethionates such as the acyl isethionates, N-acyl taurates, fatty acid amides of methyl tauride, alkyl succinates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C, ⁇ -C, ⁇ monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C.--C , , diesters), N-acyl sarcosinates.
  • Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tallow oil.
  • the anionic sulphonate surfactants include the salts of C5-C20 linear or branched alkylbenzene sulphonates, alkyl ester sulphonates, C6-C22 primary or secondary alkane sulphonates, Cg-C24 olefin sulphonates, sulphonated polycarboxylic acids, and any mixtures thereof.
  • Preferred salts are sodium and potassium salts.
  • alkyl ester sulphonated surfactant are also suitable for the invention, preferably those of formula
  • R* is a Cg-C22 hydrocarbyl
  • R 2 is a Cj-C6 alkyl
  • A is a C6-C22 alkylene
  • alkenylene x is 0 or 1
  • M is a cation.
  • the counterion M is preferably sodium, potassium or ammonium.
  • the alkyl ester sulphonated surfactant is preferably a ⁇ -sulpho alkyl ester of the formula above, whereby thus x is 0.
  • R ! is an alkyl or alkenyl group of from 10 to 22, preferably 16 C atoms and x is preferably 0.
  • R 2 is preferably ethyl or more preferably methyl.
  • Rl of the ester is derived from unsaturated fatty acids, with preferably 1, 2 or 3 double bonds. It can also be preferred that R 1 of the ester is derived from a natural occurring fatty acid, preferably palmic acid or stearic acid or mixtures thereof.
  • the anionic sulphate surfactant herein include the linear and branched primary and secondary alkyl sulphates and disulphates, alkyl ethoxysulphates having an average ethoxylation number of 3 or below, fatty oleoyl glycerol sulphates, alkyl phenol ethylene oxide ether sulphates, the C5-C17 acyl-N-(C ⁇ -C4 alkyl) and -N-(C]-C2 hydroxyalkyl) glucamine sulphates, and sulphates of alkylpolysaccharides.
  • Primary alkyl sulphate surfactants are preferably selected from the linear and branched primary C ] Q-C ⁇ g alkyl sulphates, more preferably the C ⁇ ⁇ -C 5 linear or branched chain alkyl sulphates, or more preferably the C12-C14 linear chain alkyl sulphates.
  • Preferred secondary alkyl sulphate surfactant are of the formula
  • R 3 is a C 8 -C 20 hydrocycarbyl
  • R 4 is a hydrocycarbyl
  • M is a cation.
  • Alkyl ethoxy sulphate surfactants are preferably selected from the group consisting of the Cio-Cj g alkyl sulphates which have been ethoxylated with from 0.5 to 3 moles of ethylene oxide per molecule. More preferably, the alkyl ethoxysulphate surfactant is a C ⁇ ⁇ -C ⁇ , most preferably Cj 1-C15 alkyl sulphate which has been ethoxylated with from
  • a particularly preferred aspect of the invention employs mixtures of the preferred alkyl sulphate and alkyl ethoxysulphate surfactants.
  • Preferred salts are sodium and potassium salts.
  • Preferred mid-chain branched primary alkyl_sulfate surfactants for use herein are of the formula
  • These surfactants have a linear primary alkyl sulfate chain backbone (i.e., the longest linear carbon chain which includes the sulfated carbon atom) which preferably comprises from 12 to 19 carbon atoms and their branched primary alkyl moieties comprise preferably a total of at least 14 and preferably no more than 20, carbon atoms.
  • the average total number of carbon atoms for the branched primary alkyl moieties is preferably within the range of from greater than 14.5 to about 17.5.
  • the surfactant system preferably comprises at least one branched primary alkyl sulfate surfactant compound having a longest linear carbon chain of not less than 12 carbon atoms or not more than 19 carbon atoms, and the total number of carbon atoms including branching must be at least 14, and further the average total number of carbon atoms for the branched primary alkyl moiety is within the range of greater than 14.5 to about 17.5.
  • R, Rl, and R 2 are each independently selected from hydrogen and Cj-C alkyl group (preferably hydrogen or Ci -C2 alkyl, more preferably hydrogen or methyl, and most preferably methyl), provided R, R*, and R 2 are not all hydrogen. Further, when z is 1, at least R or Rl is not hydrogen.
  • M is hydrogen or a salt forming cation depending upon the method of synthesis.
  • w is an integer from 0 to 13;
  • x is an integer from 0 to 13;
  • y is an integer from 0 to 13;
  • z is an integer of at least 1 ;
  • w + x + y + z is an integer from 8 to 14.
  • a preferred mid-chain branched primary alkyl sulfate surfactant is, a C16 total carbon primary alkyl sulfate surfactant having 13 carbon atoms in the backbone and having 1, 2, or 3 branching units (i.e., R, Rl and/or R 2 ) of in total 3 carbon atoms, (whereby thus the total number of carbon atoms is at least 16).
  • Preferred branching units can be one propyl branching unit or three methyl branching units.
  • Another preferred surfactant are branched primary alkyl sulfates having the formula
  • dianionic surfactants are also useful anionic surfactants for the present invention, in particular those of formula
  • R is an, optionally substituted, alkyl, alkenyl, aryl, alkaryl, ether, ester, amine or amide group of chain length C ⁇ to C28, preferably C3 to C24, most preferably Cg to C20, or hydrogen;
  • a and B are independently selected from alkylene, alkenylene, (poly) alkoxylene, hydroxyalkylene, arylalkylene or amido alkylene groups of chain length C ⁇ to C28 preferably C ⁇ to C5, most preferably C ⁇ or C2, or a covalent bond, and preferably
  • a and B in total contain at least 2 atoms; A, B, and R in total contain from 4 to about 31 carbon atoms; X and Y are anionic groups selected from the group comprising carboxylate, and preferably sulfate and sulfonate, z is 0 or preferably 1 ; and M is a cationic moiety, preferably a substituted or unsubstituted ammonium ion, or an alkali or alkaline earth metal ion.
  • the most preferred dianionic surfactant has the formula as above where R is an alkyl group of chain length from C ⁇ Q to C ⁇ g, A and B are independently C ⁇ or C2, both X and
  • Y are sulfate groups
  • M is a potassium, ammonium, or a sodium ion.
  • Preferred dianionic surfactants herein include:
  • R is a straight or branched chain alkyl or alkenyl group of chain length from about C4 to about C 20
  • R is a straight or branched chain alkyl or alkenyl group of chain length from about C4 to about Cjg; preferred R are selected from octanyl, nonanyl, decyl, dodecyl, tetradecyl, hexadecyl, octadecyl, and mixtures thereof; and (c) 1,5 disulphate compounds, preferably 1,5 C9-C23 straight or branched chain alkyl or alkenyl disulphates, more preferably having the formula:
  • R is a straight or branched chain alkyl or alkenyl group of chain length from about C4 to about C1 g.
  • dianionic surfactants of the invention are alkoxylated dianionic surfactants.
  • the alkoxylated dianionic surfactants of the invention comprise a structural skeleton of at least five carbon atoms, to which two anionic substituent groups spaced at least three atoms apart are attached. At least one of said anionic substituent groups is an alkoxy- linked sulphate or sulphonate group.
  • Said structural skeleton can for example comprise any of the groups consisting of alkyl, substituted alkyl, alkenyl, aryl, alkaryl, ether, ester, amine and amide groups.
  • Preferred alkoxy moieties are ethoxy, propoxy, and combinations thereof.
  • the structural skeleton preferably comprises from 5 to 32, preferably 7 to 28, most preferably 12 to 24 atoms.
  • the structural skeleton comprises only carbon- containing groups and more preferably comprises only hydrocarbyl groups.
  • the structural skeleton comprises only straight or branched chain alkyl groups.
  • the structural skeleton is preferably branched. Preferably at least 10 % by weight of the structural skeleton is branched and the branches are preferably from 1 to 5, more preferably from 1 to 3, most preferably from 1 to 2 atoms in length (not including the sulphate or sulphonate group attached to the branching).
  • a preferred alkoxylated dianionic surfactant has the formula
  • R is an, optionally substituted, alkyl, alkenyl, aryl, alkaryl, ether, ester, amine or amide group of chain length Cj to C28 > preferably C3 to C24, most preferably Cg to C20 > or hydrogen;
  • a and B are independently selected from, optionally substituted, alkyl and alkenyl group of chain length C ⁇ to C28, preferably C ⁇ to C5, most preferably Cj or C2, or a covalent bond;
  • EO/PO are alkoxy moieties selected from ethoxy, propoxy, and mixed ethoxy/propoxy groups, wherein n and m are independently within the range of from about 0 to about 10, with at least m or n being at least 1 ;
  • a and B in total contain at least 2 atoms;
  • A, B, and R in total contain from 4 to about 31 carbon atoms;
  • X and Y are anionic groups selected from the group consisting of sulphate and sulphonate
  • the most preferred alkoxylated dianionic surfactant has the formula as above where R is an alkyl group of chain length from C ⁇ Q to C ⁇ g, A and B are independently C ⁇ or C2, n and m are both 1 , both X and Y are sulfate groups, and M is a potassium, ammonium, or a sodium ion.
  • Preferred alkoxylated dianionic surfactants herein include: ethoxylated and/or propoxylated disulphate compounds, preferably C10-C24 straight or branched chain alkyl or alkenyl ethoxylated and/or propoxylated disulphates, more preferably having the formulae: wherein R is a straight or branched chain alkyl or alkenyl group of chain length from about C6 to about C ⁇ g; EO/PO are alkoxy moieties selected from ethoxy, propoxy, and mixed ethoxy/propoxy groups; and n and m are independently within the range of from about 0 to about 10 (preferably from about 0 to about 5), with at least m or n being 1.
  • Suitable anionic carboxylate surfactants include the alkyl ethoxy carboxylates, the alkyl polyethoxy polycarboxylate surfactants and the soaps ('alkyl carboxyls'), especially certain secondary soaps as described herein.
  • Suitable alkyl ethoxy carboxylates include those with the formula RO(CH2CH2 ⁇ ) x
  • R is a Cg to Cjg alkyl group
  • x ranges from O to 10
  • the ethoxylate distribution is such that, on a weight basis, the amount of material where x is 0 is less than 20 % and M is a cation.
  • Suitable alkyl polyethoxy polycarboxylate surfactants include those having the formula RO-(CHR ⁇ -CHR2-O)-R3 wherein R is a Cg to Ci g alkyl group, x is from 1 to 25, R ⁇ and R2 are selected from the group consisting of hydrogen, methyl acid radical, succinic acid radical, hydroxysuccinic acid radical, and mixtures thereof, and R3 is selected from the group consisting of hydrogen, substituted or unsubstituted hydrocarbon having between 1 and 8 carbon atoms, and mixtures thereof.
  • Suitable soap surfactants include the secondary soap surfactants which contain a carboxyl unit connected to a secondary carbon.
  • Preferred secondary soap surfactants for use herein are water-soluble members selected from the group consisting of the water-soluble salts of 2-methyl-l-undecanoic acid, 2-ethyl-l-decanoic acid, 2-propyl-l-nonanoic acid, 2- butyl- 1-octanoic acid and 2-pentyl-l-heptanoic acid.
  • Certain soaps may also be included as suds suppressors.
  • alkali metal sarcosinates of formula R-CON (Rl) CH2 COOM, wherein R is a C5-C17 linear or branched alkyl or alkenyl group, Rl is a C1-C4 alkyl group and M is an alkali metal ion.
  • R is a C5-C17 linear or branched alkyl or alkenyl group
  • Rl is a C1-C4 alkyl group
  • M is an alkali metal ion.
  • any alkoxylated nonionic surfactants are suitable herein.
  • the ethoxylated and propoxylated nonionic surfactants are preferred.
  • Preferred alkoxylated surfactants can be selected from the classes of the nonionic condensates of alkyl phenols, nonionic ethoxylated alcohols, nonionic ethoxylated/propoxylated fatty alcohols, nonionic ethoxylate/propoxylate condensates with propylene glycol, and the nonionic ethoxylate condensation products with propylene oxide/ethylene diamine adducts.
  • the condensation products of aliphatic alcohols with from 1 to 25 moles of alkylene oxide, particularly ethylene oxide and/or propylene oxide, are suitable for use herein.
  • the alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from 6 to 22 carbon atoms.
  • Particularly preferred are the condensation products of alcohols having an alkyl group containing from 8 to 20 carbon atoms with from 2 to 10 moles of ethylene oxide per mole of alcohol.
  • Polyhydroxy fatty acid amides suitable for use herein are those having the structural formula R ⁇ CONRlZ wherein : Rl is H, C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, ethoxy, propoxy, or a mixture thereof, preferable C1-C4 alkyl, more preferably Cj or C2 alkyl, most preferably C ⁇ alkyl (i.e., methyl); and R is a C5-C31 hydrocarbyl, preferably straight-chain C5-C19 alkyl or alkenyl, more preferably straight-chain C9-C17 alkyl or alkenyl, most preferably straight-chain Cj 1-C17 alkyl or alkenyl, or mixture thereof; and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative (preferably ethoxylated or propoxylated) thereof.
  • Z preferably
  • Suitable fatty acid amide surfactants include those having the formula: R ⁇ CON(R ⁇ )2 wherein R° is an alkyl group containing from 7 to 21, preferably from 9 to 17 carbon atoms and each R? is selected from the group consisting of hydrogen, C1-C4 alkyl, C ⁇ - C4 hydroxyalkyl, and -(C2H4 ⁇ ) x H, where x is in the range of from 1 to 3.
  • alkylpolysaccharides for use herein are disclosed in U.S. Patent 4,565,647, Llenado, issued January 21, 1986, having a hydrophobic group containing from 6 to 30 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group containing from 1.3 to 10 saccharide units.
  • Preferred alkylpolyglycosides have the formula:
  • R 2 is selected from the group consisting of alkyl, alkylphenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from 10 to 18 carbon atoms; n is 2 or 3; t is from 0 to 10, and x is from 1.3 to 8.
  • the glycosyl is preferably derived from glucose.
  • Suitable amphoteric surfactants for use herein include the amine oxide surfactants and the alkyl amphocarboxylic acids.
  • Suitable amine oxides include those compounds having the formula R3(OR4) X NO(R->)2 wherein Ry is selected from an alkyl, hydroxyalkyl, acylamidopropoyl and alkyl phenyl group, or mixtures thereof, containing from 8 to 26 carbon atoms; R4 is an alkylene or hydroxyalkylene group containing from 2 to 3 carbon atoms, or mixtures thereof; x is from 0 to 5, preferably from 0 to 3; and each R ⁇ is an alkyl or hydroxyalkyl group containing from 1 to 3, or a polyethylene oxide group containing from 1 to 3 ethylene oxide groups.
  • Preferred are Ci Q-Cj alkyl dimethylamine oxide, and C ⁇ o-18 acylamido alkyl dimethylamine oxide.
  • a suitable example of an alkyl aphodicarboxylic acid is Miranol(TM) C2M Cone, manufactured by Miranol, Inc., Dayton, NJ.
  • Zwitterionic surfactants can also be incorporated into the detergent compositions in accord with the invention. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or derivatives of quaternary ammonium, quaternary phosphonium or tertiary sulfonium compounds. Betaine and sultaine surfactants are exemplary zwitterionic surfactants for use herein.
  • Suitable betaines are those compounds having the formula R(R')2N + R2COO ⁇ wherein R is a Cg-Cj g hydrocarbyl group, each Rl is typically C1-C3 alkyl, and R 2 is a C1-C5 hydrocarbyl group.
  • Preferred betaines are Cj2-18 dimethyl-ammonio hexanoate and the ClO-18 acylamidopropane (or ethane) dimethyl (or diethyl) betaines.
  • Complex betaine surfactants are also suitable for use herein.
  • Suitable cationic surfactants to be used in the detergent herein include the quaternary ammonium surfactants.
  • the quaternary ammonium surfactant is a mono Cg-
  • N positions are substituted by methyl, hydroxyethyl or hydroxypropyl groups.
  • Preferred are also the mono-alkoxylated and bis-alkoxylated amine surfactants.
  • cationic ester surfactants Another suitable group of cationic surfactants which can be used in the detergent compositions or components thereof herein are cationic ester surfactants.
  • the cationic ester surfactant is a, preferably water dispersible, compound having surfactant properties comprising at least one ester (i.e. -COO-) linkage and at least one cationically charged group.
  • Suitable cationic ester surfactants including choline ester surfactants, have for example been disclosed in US Patents No.s 4228042, 4239660 and 4260529.
  • ester linkage and cationically charged group are separated from each other in the surfactant molecule by a spacer group consisting of a chain comprising at least three atoms (i.e. of three atoms chain length), preferably from three to eight atoms, more preferably from three to five atoms, most preferably three atoms.
  • the atoms forming the spacer group chain are selected from the group consisting of carbon, nitrogen and oxygen atoms and any mixtures thereof, with the proviso that any nitrogen or oxygen atom in said chain connects only with carbon atoms in the chain.
  • spacer groups having, for example, -O-O- (i.e.
  • spacer groups having, for example -CH2-O- CH2- and -CH2-NH-CH2- linkages are included.
  • the spacer group chain comprises only carbon atoms, most preferably the chain is a hydrocarbyl chain.
  • cationic mono-alkoxylated amine surfactant preferably of the general formula I:
  • R is an alkyl or alkenyl moiety containing from about 6 to about 18 carbon atoms, preferably 6 to about 16 carbon atoms, most preferably from about 6 to about 14 carbon atoms;
  • R 2 and R ⁇ are each independently alkyl groups containing from one to about three carbon atoms, preferably methyl, most preferably both R 2 and R ⁇ are methyl groups;
  • R ⁇ is selected from hydrogen (preferred), methyl and ethyl;
  • X" is an anion such as chloride, bromide, methylsulfate, sulfate, or the like, to provide electrical neutrality;
  • A is a alkoxy group, especially a ethoxy, propoxy or butoxy group; and
  • p is from 0 to about 30, preferably 2 to about 15, most preferably 2 to about 8.
  • Particularly preferred ApR ⁇ groups are — CH 2 CH 2 OH, — CH 2 CH 2 CH 2 OH, — CH 2 CH(CH 3 )OH and —
  • R 1 groups are linear alkyl groups. Linear Rl groups having from 8 to 14 carbon atoms are preferred.
  • Another highly preferred cationic mono-alkoxylated amine surfactants for use herein are of the formula
  • Rl is Cjo-Cig hydrocarbyl and mixtures thereof, especially C1Q-C14 alkyl, preferably C ⁇ Q an d Cj2 alkyl, and X is any convenient anion to provide charge balance, preferably chloride or bromide.
  • compounds of the foregoing type include those wherein the ethoxy (CH2CH2O) units (EO) are replaced by butoxy, isopropoxy [CH(CH3)CH2O] and [CH2CH(CH3 ⁇ ] units (i-Pr) or n-propoxy units (Pr), or mixtures of EO and/or Pr and/or i-Pr units.
  • EO ethoxy
  • i-Pr isopropoxy units
  • Pr n-propoxy units
  • the levels of the cationic mono-alkoxylated amine surfactants used in detergent compositions of the invention is preferably from 0.1 %> to 20%, more preferably from 0.2% to 7%, most preferably from 0.3% to 3.0% by weight of the composition.
  • the cationic bis-alkoxylated amine surfactant preferably has the general formula II:
  • Rl is an alkyl or alkenyl moiety containing from about 8 to about 18 carbon atoms, preferably 10 to about 16 carbon atoms, most preferably from about 10 to about 14 carbon atoms;
  • R 2 is an alkyl group containing from one to three carbon atoms, preferably methyl;
  • R ⁇ and R ⁇ can vary independently and are selected from hydrogen (preferred), methyl and ethyl,
  • X" is an anion such as chloride, bromide, methylsulfate, sulfate, or the like, sufficient to provide electrical neutrality.
  • a and A' can vary independently and are each selected from C1-C4 alkoxy, especially ethoxy, (i.e., -CH2CH2O-), propoxy, butoxy and mixtures thereof; p is from 1 to about 30, preferably 1 to about 4 and q is from 1 to about 30, preferably 1 to about 4, and most preferably both p and q are 1.
  • Rl is C10-C18 hydrocarbyl and mixtures thereof, preferably CJO * Cj2 > C14 alkyl and mixtures thereof.
  • X is any convenient anion to provide charge balance, preferably chloride.
  • cationic bis-alkoxylated amine surfactants useful herein include compounds of the formula:
  • Rl is CjQ-Cig hydrocarbyl, preferably C10-C14 alkyl, independently p is 1 to about 3 and q is 1 to about 3, R 2 is C1-C3 alkyl, preferably methyl, and X is an anion, especially chloride or bromide.
  • Other compounds of the foregoing type include those wherein the ethoxy (CH2CH2O) units (EO) are replaced by butoxy (Bu) isopropoxy [CH(CH3)CH2 ⁇ ] and
  • the water insoluble builder comprises in particular aluminosilicates.
  • The_aluminosilicates herein include zeolites which have the unit cell formula
  • aluminosilicates are in preferably in hydrated form and are preferably crystalline, containing from 10% to 28%>, more preferably from 18% to 22% water in bound form. However, it may be useful to incorporate overdried aluminosilictaes.
  • the aluminosilicates can be naturally occurring materials, but are preferably synthetically derived. Synthetic crystalline aluminosilicate ion exchange materials are available under the designations Zeolite A, Zeolite B, Zeolite P, Zeolite X, Zeolite HS and mixtures thereof. Zeolite A has the formula
  • Zeolite X has the formula Nagg [(Al ⁇ 2)86(Si ⁇ 2)i06J- 276 H 2 O.
  • Effervescence System Any effervescence system known in the art can be used in the composition of the invention.
  • a preferred effervescence system comprises an acid source, capable of reacting with an alkali source in the presence of water to produce a gas.
  • the acid source is preferably present at a level of from 0.5% o 35%, more preferably from 1.0% or even 2% to 20% or even form 4% to 20% by weight of the composition.
  • the acid source or part thereof and the alkali source or part thereof are comprised in an intimate mixture, for example in the form of a compacted particle.
  • the molecular ratio of the acid source to the alkali source present in such a mixture is preferably from 50:1 to 1 :50, more preferably from 20:1 to 1 :20 more preferably from 10:1 to 1 :10, more preferably from 5:1 to 1 :3, more preferably from 3:1 to 1 :2, more preferably from 2:1 to 1 :2.
  • such a particle is present and in addition thereto one or more separate acid sources and one or more separate alkali sources
  • the acid source component may be any organic, mineral or inorganic acid, or a derivative thereof, or a mixture thereof.
  • the acid source component comprises an organic acid.
  • the acid compound is preferably substantially anhydrous or non-hygroscopic and the acid is preferably water-soluble. It may be preferred that the acid source is overdried. Some of these acids may be water-soluble builders, as described above and should be considered part of the builder system of the compositions herein, whilst also providing effervescing.
  • Suitable acids source components include citric, malic, maleic, fumaric, aspartic, glutaric, tartaric succinic or adipic acid, monosodium phosphate, boric acid, or derivative thereof. Citric acid, maleic or malic acid are especially preferred. Most preferably, the acid source provides acidic compounds which have an average particle size in the range of from about 75 microns to 1 180 microns, more preferably from 150 microns to about 710 microns, calculated by sieving a sample of the source of acidity on a series of Tyler sieves.
  • the effervescence system preferably comprises an alkali source.
  • any alkali source which has the capacity to react with the acid source to produce a gas may be present in the particle, which may be any gas known in the art, including nitrogen oxygen and carbondioxide gas.
  • Preferred can be perhydrate bleaches, including perborate, and silicate material.
  • the alkali source is preferably substantially anhydrous or non- hydroscopic. It may be preferred that the alkali source is overdried.
  • this gas is carbon dioxide
  • the alkali source is a preferably a source of carbonate, which can be any source of carbonate known in the art.
  • the carbonate source is a carbonate salt.
  • preferred carbonates are the alkaline earth and alkali metal carbonates, including sodium or potassium carbonate, bicarbonate and sesqui-carbonate and any mixtures thereof with ultra-fine calcium carbonate such as are disclosed in German Patent Application No. 2,321,001 published on November 15, 1973.
  • Alkali metal percarbonate salts are also suitable sources of carbonate species, which may be present combined with one or more other carbonate sources.
  • the carbonate and bicarbonate preferably have an amorphous structure.
  • the carbonate and or bicarbonates may be coated with coating materials.
  • the particles of carbonate and bicarbonate can have a mean particle size of 75 microns or preferably 150 ⁇ m or greater, more preferably of 250 ⁇ m or greater, preferably 500 ⁇ m or greater.
  • the carbonate salt is such that fewer than 20% (by weight) of the particles have a particle size below 500 ⁇ m, calculated by sieving a sample of the carbonate or bicarbonate on a series of Tyler sieves.
  • the fewer than 60% or even 25% of the particles have a particle size below 150 ⁇ m, whilst fewer than 5% has a particle size of more than 1.18 mm, more preferably fewer than 20% have a particle size of more than 212 ⁇ m, calculated by sieving a sample of the carbonate or bicarbonate on a series of Tyler sieves.
  • compositions herein may also comprise an alkali source when no effervescence is required or when no acid source is present, but for example to provide the required pH of the composition or the wash water.
  • carbonate salts may be present in the detergent composition of the invention.
  • compositions herein may contain additional detergent components.
  • additional detergent components The precise nature of these additional components, and levels of inco ⁇ oration thereof will depend on the physical form of the compositions comprising the builder component and the precise nature of the washing operation for which it is to be used.
  • Additional ingredients include bleach, enzymes, suds suppressors, lime soap, dispersants, soil suspension and anti-redeposition agents soil releasing agents, perfumes, brighteners, photobleaching agents and additional corrosion inhibitors.
  • compositions herein is an oxygen bleach, preferably comprising a hydrogen peroxide source and a bleach precursor or activator.
  • a preferred source of hydrogen peroxide is a perhydrate bleach, such as metal perborates, more preferably metal percarbonates, particularly the sodium salts.
  • a perhydrate bleach such as metal perborates, more preferably metal percarbonates, particularly the sodium salts.
  • Potassium peroxymonopersulfate, sodium per is another optional inorganic perhydrate salt of use in the detergent compositions herein.
  • Perborate can be mono or tetra hydrated.
  • Sodium percarbonate has the formula corresponding to 2Na2C ⁇ 3-3H2 ⁇ 2, and is available commercially as a crystalline solid.
  • percarbonate salts are used herein and in particular percarbonate salts which are coated.
  • Suitable coating agent are known in the art, and include silicates, magnesium salts and carbonates salts and mixtures thereof.
  • a preferred feature of the composition herein is an organic peroxyacid bleaching system.
  • the bleaching system contains a hydrogen peroxide source and an organic peroxyacid bleach precursor compound.
  • the production of the organic peroxyacid occurs by an in situ reaction of the precursor with a source of hydrogen peroxide.
  • Preferred sources of hydrogen peroxide include inorganic perhydrate bleaches, such as the perborate bleach of the claimed invention.
  • a preformed organic peroxyacid is inco ⁇ orated directly into the composition.
  • Compositions containing mixtures of a hydrogen peroxide source and organic peroxyacid precursor in combination with a preformed organic peroxyacid are also envisaged.
  • Peroxyacid bleach precursors are compounds which react with hydrogen peroxide in a perhydrolysis reaction to produce a peroxyacid.
  • peroxyacid bleach precursors may be represented as O X - C - L
  • L is a leaving group and X is essentially any functionality, such that on perhydroloysis the structure of the peroxyacid produced is
  • Peroxyacid bleach precursor compounds are preferably inco ⁇ orated at a level of from 0.5% to 20% by weight, more preferably from 1% to 15%> by weight, most preferably from 1.5% to 10%> by weight of the detergent compositions.
  • Suitable peroxyacid bleach precursor compounds typically contain one or more N- or O- acyl groups, which precursors can be selected from a wide range of classes.
  • Suitable classes include anhydrides, esters, imides, lactams and acylated derivatives of imidazoles and oximes. Examples of useful materials within these classes are disclosed in GB-A- 1586789. Suitable esters are disclosed in GB-A-836988, 864798, 1147871, 2143231 and EP-A-0170386.
  • L group The leaving group, hereinafter L group, must be sufficiently reactive for the perhydrolysis reaction to occur within the optimum time frame (e.g., a wash cycle). However, if L is too reactive, this activator will be difficult to stabilise for use in a bleaching composition.
  • Preferred L groups are selected from the group consisting of:
  • R is an alkyl, aryl, or alkaryl group containing from 1 to
  • R 3 is an alkyl chain containing from 1 to 8 carbon atoms.
  • R 4 is H or
  • R 3 , and Y is H or a solubilizing group.
  • Any of R 1 , R3 and R 4 may be substituted by essentially any functional group including, for example alkyl, hydroxy, alkoxy, halogen, amine, nitrosyl, amide and ammonium or alkyl ammmonium groups. - + - + - + + + 3 -
  • the preferred solubilizing groups are -SO., M , -CO- M , -SO ⁇ M , -N (R ) ⁇ X and
  • M O ⁇ N(R )-, and most preferably -SO., M and -CO 2 M wherein R is an alkyl chain containing from 1 to 4 carbon atoms, M is a cation which provides solubility to the bleach activator and X is an anion which provides solubility to the bleach activator.
  • M is an alkali metal, ammonium or substituted ammonium cation, with sodium and potassium being most preferred, and X is a halide, hydroxide, methylsulfate or acetate anion.
  • Alkyl percarboxylic acid bleach precursors form percarboxylic acids on perhydrolysis.
  • Preferred precursors of this type provide peracetic acid on perhydrolysis.
  • Preferred alkyl percarboxylic precursor compounds of the imide type include the N- ,N,N1N1 tetra acetylated alkylene diamines wherein the alkylene group contains from 1 to 6 carbon atoms, particularly those compounds in which the alkylene group contains 1 , 2 and 6 carbon atoms.
  • Tetraacetyl ethylene diamine (TAED) is particularly preferred.
  • the TAED is preferably not present in the agglomerated particle of the present invention, but preferably present in the detergent composition, comprising the particle.
  • alkyl percarboxylic acid precursors include sodium 3,5,5-tri-methyl hexanoyloxybenzene sulfonate (iso-NOBS), sodium nonanoyloxybenzene sulfonate (NOBS), sodium acetoxybenzene sulfonate (ABS) and pentaacetyl glucose.
  • Amide substituted alkyl peroxyacid precursor compounds are suitable herein, including those of the following general formulae: R N — R' R _ N _ -c - - R 2 C
  • Rl is an alkyl group with from 1 to 14 carbon atoms
  • R2 is an alkylene group containing from 1 to 14 carbon atoms
  • R ⁇ is H or an alkyl group containing 1 to 10 carbon atoms and L can be essentially any leaving group.
  • Amide substituted bleach activator compounds of this type are described in EP-A-0170386.
  • Perbenzoic acid precursor compounds provide perbenzoic acid on perhydrolysis.
  • Suitable O-acylated perbenzoic acid precursor compounds include the substituted and unsubstituted benzoyl oxybenzene sulfonates, and the benzoylation products of sorbitol, glucose, and all saccharides with benzoylating agents, and those of the imide type including N-benzoyl succinimide, tetrabenzoyl ethylene diamine and the N-benzoyl substituted ureas.
  • Suitable imidazole type perbenzoic acid precursors include N-benzoyl imidazole and N-benzoyl benzimidazole.
  • Other useful N-acyl group-containing perbenzoic acid precursors include N-benzoyl pyrrolidone, dibenzoyl taurine and benzoyl pyroglutamic acid.
  • the detergent composition may contain, in addition to, or as an alternative to, an organic peroxyacid bleach precursor compound, a preformed organic peroxyacid , typically at a level of from 1% to 15% by weight, more preferably from 1% to 10% by weight of the composition.
  • a preferred class of organic peroxyacid compounds are the amide substituted compounds of the following general formulae: R 1 — C — N — R 2 — C — OOH R 1 N R' C - OOH
  • Rl is an alkyl, aryl or alkaryl group with from 1 to 14 carbon atoms
  • R is an alkylene, arylene, and alkarylene group containing from 1 to 14 carbon atoms
  • R ⁇ is H or an alkyl, aryl, or alkaryl group containing 1 to 10 carbon atoms.
  • Amide substituted organic peroxyacid compounds of this type are described in EP-A-0170386.
  • organic peroxyacids include diacyl and tetraacylperoxides, especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid.
  • diacyl and tetraacylperoxides especially diperoxydodecanedioc acid, diperoxytetradecanedioc acid and diperoxyhexadecanedioc acid.
  • Mono- and diperazelaic acid, mono- and diperbrassylic acid and N- phthaloylaminoperoxicaproic acid are also suitable herein.
  • Heavy metal ion sequestrant are also useful additional ingredients herein.
  • heavy metal ion sequestrant it is meant herein components which act to sequester (chelate) heavy metal ions. These components may also have a limited calcium and magnesium chelation capacity, but preferentially they show selectivity to binding heavy metal ions such as iron, manganese and copper. The are thus not considered builders for the pu ⁇ ose of the invention.
  • Heavy metal ion sequestrants are generally present at a level of from 0.005%) to 10%, preferably from 0.1% to 5%, more preferably from 0.25% to 7.5% and most preferably from 0.3%> to 2% by weight of the compositions.
  • Suitable heavy metal ion sequestrants for use herein include organic phosphonates, such as the amino alkylene poly (alkylene phosphonates), alkali metal ethane 1 -hydroxy disphosphonates and nitrilo trimethylene phosphonates.
  • organic phosphonates such as the amino alkylene poly (alkylene phosphonates), alkali metal ethane 1 -hydroxy disphosphonates and nitrilo trimethylene phosphonates.
  • Preferred among the above species are diethylene triamine penta (methylene phosphonate), ethylene diamine tri (methylene phosphonate) hexamethylene diamine tetra (methylene phosphonate) and hydroxy-ethylene 1,1 diphosphonate, 1,1 hydroxyethane diphosphonic acid and 1,1 hydroxyethane dimethylene phosphonic acid.
  • Suitable heavy metal ion sequestrant for use herein include nitrilotriacetic acid and polyaminocarboxylic acids such as ethylenediaminotetracetic acid, ethylenediamine disuccinic acid, ethylenediamine diglutaric acid, 2-hydroxypropylenediamine disuccinic acid or any salts thereof.
  • Suitable heavy metal ion sequestrants for use herein are iminodiacetic acid derivatives such as 2-hydroxyethyl diacetic acid or glyceryl imino diacetic acid, described in EP-A-317,542 and EP-A-399,133.
  • iminodiacetic acid-N-2-hydroxypropyl sulfonic acid and aspartic acid N-carboxymethyl N-2-hydroxypropyl-3 -sulfonic acid sequestrants described in EP-A-516,102 are also suitable herein.
  • EP-A-476,257 describes suitable amino based sequestrants.
  • EP-A-510,331 describes suitable sequestrants derived from collagen, keratin or casein.
  • EP-A- 528,859 describes a suitable alkyl iminodiacetic acid sequestrant. Dipicolinic acid and 2-phosphonobutane-l,2,4-tricarboxylic acid are also suitable.
  • Glycinamide- N,N'-disuccinic acid (GADS), ethylenediamine-N-N'-diglutaric acid (EDDG) and 2- hydroxypropylenediamine-N-N'-disuccinic acid (HPDDS) are also suitable.
  • diethylenetriamine pentacetic acid ethylenediamine-N,N'- disuccinic acid (EDDS) and 1,1 hydroxyethane diphosphonic acid or the alkali metal, alkaline earth metal, ammonium, or substituted ammonium salts thereof, or mixtures thereof.
  • EDDS ethylenediamine-N,N'- disuccinic acid
  • 1,1 hydroxyethane diphosphonic acid or the alkali metal, alkaline earth metal, ammonium, or substituted ammonium salts thereof, or mixtures thereof.
  • Another preferred ingredient useful herein is one or more additional enzymes.
  • Preferred additional enzymatic materials include the commercially available lipases, cutinases, amylases, neutral and alkaline proteases, cellulases, endolases, esterases, pectinases, lactases and peroxidases conventionally inco ⁇ orated into detergent compositions. Suitable enzymes are discussed in US Patents 3,519,570 and 3,533,139.
  • Organic polymeric compounds are preferred additional components of the compositions herein.
  • organic polymeric compound it is meant herein essentially any polymeric organic compound commonly used as binder, dispersants, and anti-redeposition and soil suspension agents in detergent compositions, including any of the high molecular weight organic polymeric compounds described as clay flocculating agents herein, including quatemised ethoxylated (poly) amine clay-soil removal/ anti-redeposition agent, not being polymeric polycarboxylte polymers.
  • Organic polymeric compound is typically inco ⁇ orated in the detergent compositions of the invention at a level of from 0.01% to 30%, preferably from 0.1% to 15%, most preferably from 0.5% to 10%o by weight of the compositions.
  • polyamino compounds are useful herein including those derived from aspartic acid such as those disclosed in EP-A-305282, EP-A-305283 and EP-A-351629.
  • Te ⁇ olymers containing monomer units selected from maleic acid, acrylic acid, polyaspartic acid and vinyl alcohol, particularly those having an average molecular weight of from 5,000 to 10,000, are also suitable herein.
  • organic polymeric compounds suitable for inco ⁇ oration in the detergent compositions herein include cellulose derivatives such as methylcellulose, carboxymethylcellulose, hydroxypropylmethylcellulose and hydroxyethylcellulose.
  • organic polymeric compounds are the polyethylene glycols, particularly those of molecular weight 1000- 10000, more particularly 2000 to 8000 and most preferably about 4000.
  • Highly preferred polymeric components herein are cotton and non-cotton soil release polymer according to U.S. Patent 4,968,451, Scheibel et al., and U.S. Patent 5,415,807, Gosselink et al., and in particular according to US application no.60/051517.
  • Another organic compound which is a preferred clay dispersant anti-redeposition agent, for use herein, can be the ethoxylated cationic monoamines and diamines of the formula:
  • X is a nonionic group selected from the group consisting of H, C1-C4 alkyl or hydroxyalkyl ester or ether groups, and mixtures thereof
  • a is from 0 to 20, preferably from 0 to 4 (e.g. ethylene, propylene, hexamethylene)
  • Other dispersants/ anti-redeposition agents for use herein are described in EP-B-011965 and US 4,659,802 and US 4,664,848.
  • the detergent compositions of the invention when formulated for use in machine washing compositions, may comprise a suds suppressing system present at a level of from 0.01% to 15%, preferably from 0.02% to 10%, most preferably from 0.05% to 3% by weight of the composition.
  • Suitable suds suppressing systems for use herein may comprise essentially any known antifoam compound, including, for example silicone antifoam compounds and 2-alkyl alcanol antifoam compounds.
  • antifoam compound any compound or mixtures of compounds which act such as to depress the foaming or sudsing produced by a solution of a detergent composition, particularly in the presence of agitation of that solution.
  • Particularly preferred antifoam compounds for use herein are silicone antifoam compounds defined herein as any antifoam compound including a silicone component. Such silicone antifoam compounds also typically contain a silica component.
  • silicone antifoam compounds as used herein, and in general throughout the industry, encompasses a variety of relatively high molecular weight polymers containing siloxane units and hydrocarbyl group of various types.
  • Preferred silicone antifoam compounds are the siloxanes, particularly the polydimethylsiloxanes having trimethylsilyl end blocking units.
  • Suitable antifoam compounds include the monocarboxylic fatty acids and soluble salts thereof. These materials are described in US Patent 2,954,347, issued September 27, 1960 to Wayne St. John.
  • the monocarboxylic fatty acids, and salts thereof, for use as suds suppressor typically have hydrocarbyl chains of 10 to 24 carbon atoms, preferably 12 to 18 carbon atoms.
  • Suitable salts include the alkali metal salts such as sodium, potassium, and lithium salts, and ammonium and alkanolammonium salts.
  • Suitable antifoam compounds include, for example, high molecular weight fatty esters (e.g. fatty acid triglycerides), fatty acid esters of monovalent alcohols, aliphatic C18- 40 ketones (e.g. stearone) N-alkylated amino triazines such as tri- to hexa- alkylmelamines or di- to tetra alkyldiamine chlortriazines formed as products of cyanuric chloride with two or three moles of a primary or secondary amine containing 1 to 24 carbon atoms, propylene oxide, bis stearic acid amide and monostearyl di-alkali metal (e.g. sodium, potassium, lithium) phosphates and phosphate esters.
  • high molecular weight fatty esters e.g. fatty acid triglycerides
  • fatty acid esters of monovalent alcohols e.g. fatty acid esters of monovalent alcohols
  • a preferred suds suppressing system comprises:
  • antifoam compound preferably silicone antifoam compound, most preferably a silicone antifoam compound comprising in combination
  • silica at a level of from 1 % to 50%, preferably 5% to 25% by weight of the silicone/silica antifoam compound;
  • silica/silicone antifoam compound is inco ⁇ orated at a level of from
  • a dispersant compound most preferably comprising a silicone glycol rake copolymer with a polyoxyalkylene content of 72-78%) and an ethylene oxide to propylene oxide ratio of from 1 :0.9 to 1 : 1.1 , at a level of from 0.5% to 10%, preferably 1% to 10% by weight;
  • a particularly preferred silicone glycol rake copolymer of this type is DCO544, commercially available from DOW Corning under the tradename DCO544;
  • an inert carrier fluid compound most preferably comprising a C ⁇ g-C ⁇ g ethoxylated alcohol with a degree of ethoxylation of from 5 to 50, preferably 8 to 15, at a level of from 5% to 80%, preferably 10% to 70%, by weight;
  • a highly preferred particulate suds suppressing system is described in EP-A-0210731 and comprises a silicone antifoam compound and an organic carrier material having a melting point in the range 50°C to 85°C, wherein the organic carrier material comprises a monoester of glycerol and a fatty acid having a carbon chain containing from 12 to 20 carbon atoms.
  • EP-A-0210721 discloses other preferred particulate suds suppressing systems wherein the organic carrier material is a fatty acid or alcohol having a carbon chain containing from 12 to 20 carbon atoms, or a mixture thereof, with a melting point of from 45°C to 80°C.
  • suds suppressing systems comprise polydimethylsiloxane or mixtures of silicone, such as polydimethylsiloxane, aluminosilicate and polycarboxylic polymers, such as copolymers of laic and acrylic acid.
  • compositions herein may also comprise from 0.01% to 10 %, preferably from 0.05% to 0.5% by weight of polymeric dye transfer inhibiting agents.
  • the polymeric dye transfer inhibiting agents are preferably selected from polyamine N- oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidonepolymers or combinations thereof, whereby these polymers can be cross-linked polymers.
  • Optical Brightener is preferably selected from polyamine N- oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidonepolymers or combinations thereof, whereby these polymers can be cross-linked polymers.
  • compositions herein also optionally contain from about 0.005% to 5% by weight of certain types of hydrophilic optical brighteners, as known in the art.
  • SRA Polymeric soil release agents, hereinafter "SRA"
  • SRA's will generally comprise from 0.01% to 10.0%>, typically from 0.1% to 5%>, preferably from 0.2% to 3.0% by weight, of the compositions.
  • Preferred SRA's typically have hydrophilic segments to hydrophilize the surface of hydrophobic fibers such as polyester and nylon, and hydrophobic segments to deposit upon hydrophobic fibers and remain adhered thereto through completion of washing and rinsing cycles, thereby serving as an anchor for the hydrophilic segments. This can enable stains occurring subsequent to treatment with the SRA to be more easily cleaned in later washing procedures.
  • Preferred SRA's include oligomeric terephthalate esters, typically prepared by processes involving at least one transesterification/oligomerization, often with a metal catalyst such as a titanium(IV) alkoxide.
  • esters may be made using additional monomers capable of being inco ⁇ orated into the ester structure through one, two, three, four or more positions, without, of course, forming a densely crosslinked overall structure.
  • Suitable SRA's include a sulfonated product of a substantially linear ester oligomer comprised of an oligomeric ester backbone of terephthaloyl and oxyalkyleneoxy repeat units and allyl-derived sulfonated terminal moieties covalently attached to the backbone, for example as described in U.S. 4,968,451, November 6, 1990 to J.J. Scheibel and E.P. Gosselink.
  • ester oligomers can be prepared by: (a) ethoxylating allyl alcohol; (b) reacting the product of (a) with dimethyl terephthalate (“DMT”) and 1,2-propylene glycol (“PG”) in a two-stage transesterification/oligomerization procedure; and (c) reacting the product of (b) with sodium metabisulfite in water.
  • DMT dimethyl terephthalate
  • PG 1,2-propylene glycol
  • SRA's include the nonionic end- capped 1 ,2-propylene/polyoxyethylene terephthalate polyesters of U.S.
  • Gosselink et al. 4,71 1,730, December 8, 1987 to Gosselink et al., for example those produced by transesterification/oligomerization of poly(ethyleneglycol) methyl ether, DMT, PG and poly(ethyleneglycol) ("PEG").
  • SRA's include: the partly- and fully- anionic-end-capped oligomeric esters of U.S. 4,721,580, January 26, 1988 to Gosselink, such as oligomers from ethylene glycol ("EG"), PG, DMT and Na-3,6-dioxa-8- hydroxyoctanesulfonate; the nonionic-capped block polyester oligomeric compounds of U.S.
  • Gosselink for example produced from DMT, methyl (Me)-capped PEG and EG and/or PG, or a combination of DMT, EG and/or PG, Me-capped PEG and Na-dimethyl-5-sulfoisophthalate; and the anionic, especially sulfoaroyl, end-capped terephthalate esters of U.S.
  • SRA's also include: simple copolymeric blocks of ethylene terephthalate or propylene terephthalate with polyethylene oxide or polypropylene oxide terephthalate, see U.S. 3,959,230 to Hays, May 25, 1976 and U.S. 3,893,929 to Basadur, July 8, 1975; cellulosic derivatives such as the hydroxyether cellulosic polymers available as METHOCEL from Dow; the C1-C4 alkyl celluloses and C4 hydroxyalkyl celluloses, see U.S. 4,000,093,
  • methyl cellulose ethers having an average degree of substitution (methyl) per anhydroglucose unit from about 1.6 to about 2.3 and a solution viscosity of from about 80 to about 120 centipoise measured at 20°C as a 2% aqueous solution.
  • Such materials are available as METOLOSE SMI 00 and METOLOSE SM200, which are the trade names of methyl cellulose ethers manufactured by Shin-etsu Kagaku Kogyo KK.
  • SRA's include: (I) nonionic terephthalates using diisocyanate coupling agents to link polymeric ester structures, see U.S. 4,201,824. Violland et al. and U.S. 4,240,918 Lagasse et al.; and (II) SRA's with carboxylate terminal groups made by adding trimellitic anhydride to known SRA's to convert terminal hydroxyl groups to trimellitate esters. With the proper selection of catalyst, the trimellitic anhydride forms linkages to the terminals of the polymer through an ester of the isolated carboxylic acid of trimellitic anhydride rather than by opening of the anhydride linkage.
  • Either nonionic or anionic SRA's may be used as starting materials as long as they have hydroxyl terminal groups which may be esterified. See U.S. 4,525,524 Tung et al..
  • Other classes include: (III) anionic terephthalate-based SRA's of the urethane-linked variety, see U.S. 4,201,824, Violland et al.;
  • compositions of the invention include perfumes, speckles, colours or dyes, filler salts, with sodium sulfate being a preferred filler salt.
  • encapsulated perfumes preferably comprising a starch encapsulte.
  • the dye which may be used herein can be any dye for example in the form of a dye stuff or an aqueous solution of a dye stuff. It may be preferred that the dye is an aqueous solution comprising a dyestuff, at any level to obtain suitable dyeing of the particles, preferably such that levels of dye solution are obtained up to 2% by weight of the speckle particle, or more preferably up to 0.5% by weight.
  • the dye also comprising other ingredients such as organic binder materials.
  • the dyestuff can be any suitable dyestuff.
  • suitable dyestuffs include El 04 - food yellow 13 (quinoline yellow), El 10 - food yellow 3 (sunset yellow FCF), El 31 - food blue 5 (patent blue V), Ultra Marine blue (trade name), El 33 - food blue 2 (brilliant blue FCF), El 40 - natural green 3 (chlorophyll and chlo ⁇ hyllins), El 41 and Pigment green 7 (chlorinated Cu phthalocyanine).
  • Preferred dyestuffs may be Monastral Blue BV paste (trade name) and/ or Pigmasol Green (trade name).
  • compositions of the invention it may be preferred that when dyes and/ or perfumes are sprayed onto the another component, the component does not comprise spray-on nonionic alkoxylated alcohol surfactant.
  • composition of the invention thereof can be made via a variety of methods involving the mixing of ingredients, including dry-mixing, compaction such as agglomerating, extrusion, tabletting, or spray-drying of the various compounds comprised in the detergent component, or mixtures of these techniques, whereby the components herein also can be made by for example compaction, including extrusion and agglomerating, or spray-drying.
  • compositions herein can take a variety of physical solid forms including forms such as tablet, flake, pastille and bar, and preferably the composition is in the form of granules or a tablet.
  • compositions in accord with the present invention can also be used in or in combination with bleach additive compositions, for example comprising chlorine bleach.
  • the compositions preferably have a density of more than 350 gr/litre, more preferably more than 450 gr/litre or even more than 570 gr/litre.
  • Naj2(Al ⁇ 2Si ⁇ 2)i2-27H2 ⁇ having a primary particle size in the range from 0.1 to 10 micrometers (weight expressed on an anhydrous basis)
  • NaSKS-6 (I) Crystalline layered silicate of formula ⁇ - Na2Si2 ⁇ 5 0 f weight average particle size of 18 microns and at least 90% by weight being of particle size of below 65.6 microns.
  • NaSKS-6 (II) Crystalline layered silicate of formula ⁇ - Na2Si2 ⁇ 5 0 f weight average particle size of 18 microns and at least 90% by weight being of particle size of below 42.1 microns.
  • Citric acid Anhydrous citric acid
  • Silicate Amo ⁇ hous sodium silicate (SiO2:Na2O 2.0:1)
  • Protease Proteolytic enzyme having 3.3% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Savinase
  • Protease I Proteolytic enzyme, having 4% by weight of active enzyme, as described in WO 95/10591, sold by Genencor
  • Alcalase Proteolytic enzyme having 5.3% by weight of active enzyme, sold by NOVO Industries A/S
  • Amylase Amylolytic enzyme having 1.6% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Termamyl 120T
  • Amylase II Amylolytic enzyme as disclosed in PCT/ US9703635 Lipase Lipolytic enzyme, having 2.0% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Lipolase
  • Lipolytic enzyme having 2.0% by weight of active enzyme, sold by NOVO Industries A/S under the tradename Lipolase Ultra
  • Endolase Endoglucanase enzyme having 1.5% by weight of active enzyme, sold by NOVO Industries A/S PB4 : Sodium perborate tetrahydrate of nominal formula
  • DOBS Decanoyl oxybenzene sulfonate in the form of the sodium salt
  • NACA-OBS (6-nonamidocaproyl) oxybenzene sulfonate
  • DOBS Decanoyloxybenzene sulfonate in the form of the sodium salt
  • Photoactivated bleach Sulfonated zinc phthlocyanine encapsulated in or carried by soluble polymer or sulfonated alumino phthlocyanine encapsulated in or carried by soluble polymer
  • Brightener 1 Disodium 4,4'-bis(2-sulphostyryl)biphenyl
  • Brightener 2 Disodium 4,4'-bis(4-anilino-6-mo ⁇ holino-l .3.5-triazin-2- yl)amino) stilbene-2:2'-disulfonate
  • HEDP 1,1 -hydroxy ethane diphosphonic acid PEGx Polyethylene glycol, with a molecular weight of x
  • PVPVI Copolymer of polyvinylpyrolidone and vinylimidazole with an average molecular weight of 20,000
  • SRP 1 Anionically end capped poly esters
  • SRP 2 Diethoxylated poly (1, 2 propylene terephtalate) short block polymer
  • Opacifier Water based monostyrene latex mixture, sold by BASF
  • compositions are in accord with the invention.
  • compositions in accordance with the invention which may be in the form of granules or in the form of a tablet.
  • a detergent composition comprising blown powder, an agglomerate comprising crystalline layered silicate and anionic surfactant, an effervescent particle and dry-mixed bleach activator particle, sodium percarbonate, sodium citrate and suds supressor.
  • the individual particulates were prepared and dry-mixed together with gentle mixing e.g. in a Nautamixer for a period of at least 4 minutes.
  • composition of the final blown powder was as follows:-
  • the blown powder was prepared by a standard spray drying process.
  • the above ingredients were mixed into a slurry with water.
  • the aqueous slurry may be prepared by a batch or continuous process.
  • a batch mixer, or "crutcher” was used in which the various detergent components were dissolved in, or slurried with, water to provide a slurry containing 35%> water.
  • the water content my be varied from about 20%> to about 60%) by weight of water, preferably it is about from about 30% to about 40% by weight water.
  • the order of addition of the ingredients to water to form the aqueous slurry was as listed above in the final composition of the blown powder.
  • the aqueous slurry was then pumped at high pressure through atomising nozzles into a spray- drying tower where excess water was driven off, producing a flowable powder product (blown powder). Fines were screened out through a mesh.
  • An agglomerate comprising 70% SKS6 and 30% LAS was prepared by a conventional agglomeration process.
  • Effervescent Particle Particles were prepared having the following composition:
  • the particle was made via a roller compaction process.
  • the raw materials in the proportions indicated above, were fed at a press force of 80kN into a Pharmapaktor L200/50 P roller, set up with concave smooth rolls with a 0.3mm axial corrugation installed.
  • the flakes produced were then compacted using a Flake Crusher FC 200 with a mesh size selected to produce the required particle size.
  • the product was screened to remove the fines.

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Abstract

Compositions détergentes solides comportant des systèmes d'adjuvants et tensioactifs améliorés qui entraînent un meilleur mélange avec la solution de lavage et une meilleure performance de lavage. Le système d'adjuvants comporte au moins deux adjuvants, sélectionnés parmi des adjuvants hydrosolubles ou partiellement hydrosolubles ou un mélange des deux, présents à raison de 60 % à 100 % en poids du système d'adjuvants, et de 0 % à 40 % en poids du système d'adjuvants d'adjuvants non hydrosolubles, à condition que l'adjuvant aluminosilicate soit présent à raison de moins de 9 % en poids de la composition et que le silicate de sodium amorphe soit présent à raison de moins de 5 % en poids de la composition. Ladite composition comporte également au moins un constituant particulaire comprenant un mélange intime d'au moins un des tensioactifs du système tensioactif et d'au moins un des adjuvants hydrosolubles ou partiellement hydrosolubles.
EP98948562A 1998-09-25 1998-09-25 Compositions detergentes solides Withdrawn EP1115825A1 (fr)

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Cited By (2)

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WO2014037342A1 (fr) 2012-09-05 2014-03-13 Bayer Cropscience Ag Amides d'acide bicycloarylcarboxylique à action herbicide

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19943551A1 (de) * 1999-09-11 2001-03-15 Clariant Gmbh Schwerlösliches Alkalisilikat
DE19943550A1 (de) * 1999-09-11 2001-03-15 Clariant Gmbh Hochalkalisches kristallines Natriumsilikat
DE10153551A1 (de) * 2001-10-30 2003-05-22 Henkel Kgaa Im wesentlichen sedimentfrei dispergierbares Wasch- oder Reinigungsmittel
EP1754776A1 (fr) 2005-08-19 2007-02-21 The Procter and Gamble Company Procédé pour la préparation d'une composition détergente solide pour le lavage, comprenant au moins deux pas séchant
ES2415872T3 (es) 2005-08-19 2013-07-29 The Procter & Gamble Company Composición detergente para lavado de ropa, sólida que comprende un tensioactivo detersivo aniónico y una tecnología de potenciación del calcio
EP1754779B1 (fr) 2005-08-19 2012-10-17 The Procter and Gamble Company Composition de lavage en forme solide comprenant un tensioactif anionique et un support très poreux
EP1754780B1 (fr) 2005-08-19 2010-04-21 The Procter and Gamble Company Composition solide pour lavage comprenant un sulphonate d'alkylbenzène et un matériau hydratable
EP1754777B1 (fr) 2005-08-19 2010-10-20 The Procter & Gamble Company Composition détèrgente solide comprenant sulphonate d'alkylbenzene, sel de carbonate, et carboxylate polymerique
EP2519623B2 (fr) * 2009-12-30 2019-03-20 Ecolab Inc. Produits de remplacement de phosphate pour des compositions de détergent et/ou de nettoyage compatibles avec des membranes
JP5785747B2 (ja) * 2011-03-18 2015-09-30 ライオン株式会社 粒状洗剤組成物
WO2015003358A1 (fr) * 2013-07-11 2015-01-15 The Procter & Gamble Company Composition détergente pour le linge
GR20170100372A (el) * 2017-08-04 2019-04-22 Σωτηριος Στυλιανου Δημοπουλος Σκευασμα για την ταχεια αναπτυξη υμενιου αφρωδους υλης επικαλυψης στομιου λεκανης τουαλετας για την αποσβεση του πιτσιλισματος κατα την χρηση της

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9407279D0 (en) * 1994-04-13 1994-06-08 Procter & Gamble Detergent compositions
GB9407628D0 (en) * 1994-04-13 1994-06-08 Procter & Gamble Detergent compositions
DE4442977A1 (de) * 1994-12-02 1996-06-05 Henkel Kgaa Wasch- oder Reinigungsmittel mit wasserlöslichen Buildersubstanzen

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0018859A1 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013174843A1 (fr) 2012-05-24 2013-11-28 Bayer Cropscience Ag Thioamides d'acide n-(tétrazol-5-yl)- et n-(triazol-5-yl)aryle carboxylique et leur utilisation comme herbicides
WO2014037342A1 (fr) 2012-09-05 2014-03-13 Bayer Cropscience Ag Amides d'acide bicycloarylcarboxylique à action herbicide

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AU9510998A (en) 2000-04-17
MXPA01003100A (es) 2001-10-01

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