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
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/16—Organic compounds
  • C11D3/37—Polymers
  • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
  • C11D3/3738—Alkoxylated silicones
• • 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
  • C11D1/66—Non-ionic compounds
  • C11D1/72—Ethers of polyoxyalkylene glycols
• • 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
  • C11D3/0026—Low foaming or foam regulating 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
• • 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
  • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones

Definitions

• This invention relates to detergent compositions and their manufacture.
• it relates to heavy duty detergent compositions having controlled sudsing characteristics especially when used in automatic washing machines for washing clothes and the like.
• Detergent compositions normally contain surfactants which tend to produce foam when agitated in aqueous solution. For many applications, especially in automatic washing and dishwashing machines; excess foam production is a serious problem and with many effective surfactants, it is necessary to add foam suppressing or controlling agents in order to prevent suds-overflow from the machine or under-usage of product by the user.
• foam suppressing or controlling agents in order to prevent suds-overflow from the machine or under-usage of product by the user.
• consumers normally expect and prefer a certain amount of foam to be present and, indeed, research has shown that consumers are highly sensitive to a reduction in the foam level pattern. In any particular application, therefore, the optimum degree of foaming will be sufficiently low to avoid oversudsing under all conceivable washing machine temperature, load and soil conditions, but sufficiently high to meet the consumers preference for a moderate to generous level of foam.
• Detergent compositions currently sold for the European domestic automatic washing machine market generally contain up to about 12% of organic surfactant and for such compositions, foam control agents satisfying the above constraints are now well established.
• European Patent application No 46342 it is taught to use a polydimethylsiloxane/hydophobic silica foam controller in the form of a dispersion in an ethoxylated nonionic surfactant using certain siloxane-oxyalkylene copolymers as dispersing agent.
• European Patent Application No 8829 there is disclosed a foam-controlling system consisting of a major portion of wax together with a nonionic dispersing agent and hydrophobic silica.
• wax/silica/dispersant systems are also found to be deficient because of their inherently slow kinetics; in other words, the rate of release of wax/silica fails to match the rate of transport of surfactant to the air/water interface.
• these problems of foam control are found to be greatly exacerbated in concentrated surfactant systems containing a mixture of anionic and nonionic surfactant types which are known to have markedly differing foaming characteristics under varying wash temperature, product usage, soil, load and rinsing conditions.
• the present invention thus provides a detergent composition containing a high level of organic surfactant and having improved foaming characteristics across the range of wash temperature conditions. It further provides a detergent composition containing a high level of a mixture of anionic and nonionic surfactants and having improved foaming under varying wash temperature, product usage, soil, load and rinsing conditions. It also provides a detergent additive composition suitable for addition to a high active heavy duty detergent composition to provide foam control characteristics.
• a detergent additive composition comprising
• the additive composition thus comprises a mixture of preformed dispersions, a first dispersion (a) comprising polydimethylsiloxane (sometimes referred to herein as silicone) foam controlling agent in an ethoxylated nonionic surfactant of defined HLB (from 9 to 13, preferably from about 10 to about 12.5) and melting point (from 5°C to 36°C, preferably from about 10°C to about 28°C); and a second dispersion (b) comprising hydrophobic silica foam controlling agent in a water-soluble or water dispersible organic carrier also of defined melting point (from 38°C to 90°C).
• a first dispersion comprising polydimethylsiloxane (sometimes referred to herein as silicone) foam controlling agent in an ethoxylated nonionic surfactant of defined HLB (from 9 to 13, preferably from about 10 to about 12.5) and melting point (from 5°C to 36°C, preferably from about 10°C to about 28°C)
• the organic carrier comprises a second ethoxylated nonionic surfactant having an HLB in the range from about 13.5 to about 19, preferably from about 15 to about 17.5, and a melting point in the range from about 38°C to about 60°C, preferably from about 40°C to about 55°C.
• dispersion (a) can additionally contain a proportion of hydrophobic silica and dispersion (b) can additionally contain a proportion of silicone.
• dispersion (a) can additionally contain a proportion of hydrophobic silica
• dispersion (b) can additionally contain a proportion of silicone.
• the weight ratio of silicone to silica is greater than about 20:1, and is preferably from about 25:1 to about 100:1; also that the weight ratio of hydrophobic silica in dispersion (b) to that in dispersion (a) is greater than about 1:2, and is preferably from about 10:1 to about 1:1.
• the weight ratio of silicone in dispersion (b) to that in dispersion (a) is less than about 10:1 and is preferably from about 0.1:1 to about 5:1.
• the weight ratio of nonionic surfactant to silicone in dispersion (a) and of organic carrier to hydrophobic silica in dispersion (b) is also of importance for reasons of stability and dispersibility.
• the weight ratio of nonionic surfactant to silicone is from 10:1 to 100:1, preferably from about 15:1 to about 40:1; in dispersion (b), the weight ratio of organic carrier to hydrophobic silica is in the range from 10:1 to 100:1, preferably from about 15:1 to about 50:1.
• the stability of polydimethylsiloxane in dispersion (a) is maintained with the aid of a dispersion agent, preferably a siloxane-oxyalkylene copolymer having the general formula I: wherein a is 0 or an integer from 1 to 3, R is an alkyl group containing from 1 to 30 carbon atoms, or a group of formula II: wherein R' is an alkylene group containing from 1 to 6 carbon atoms, b has a value of from 1 to 100; and R" is a capping group which is selected from hydrogen, alkyl, acyl, aryl, alkaryl, aralkyl or alkenyl groups containing up to 20 carbon atoms, sulfate, sulfonate, phosphate, carboxylate, phosphonate, borate or isocyanate groups, or mixtures thereof; Y is a group having the formula III:- wherein R is as defined above and c has a value from 1 to 200;
• the organic carrier component of dispersion (b) preferably comprises an ethoxylated nonionic surfactant having an HLB of from about 13.5 to about '19.
• suitable organic carrier components include polyethyleneglycols having a molecular weight of from about 1500 to about 40,000 and, microcrystalline waxes. The latter are foam-controlling agents in their own right and are preferably added at a weight ratio of wax to silica of from about 20:1 to about 1:1, more preferably from about 15:1 to about 2:1.
• the organic carrier preferably comprises at least about 35%, more preferably at least about 45% of ethoxylated nonionic surfactant in order to promote transport of silica to the air/water interface and, in the case of wax, to provide the necessary degree of water dispersibility.
• the detergent additive compositions of the invention are utilized herein for making foam-controlled detergent compositions, either by premixing dispersion (a) and dispersion (b) prior to adding the remainder of the detergent composition, or by separately admixing dispersion (a) and dispersion (b) with the remainder of the detergent composition.
• the detergent additive composition generally constitutes from about 1% to about 30%, preferably from about 4% to about 25% of the total composition with dispersion (a) generally constituting from about 0.9% to about 25%, preferably from about 3.7% to about 23%, and dispersion (b) generally constituting from about 0.1% to about 5%, preferably from about 0.3% to about 2% by weight of tht total composition.
• the additive compositions are particularly valuable for use in detergent compositions containing anionic surfactant which is generally present in such compositions at level of from about 3% to about 30%, preferably from about 5% to about 20%, more preferably from about 8% to about 15%, with a total level of anionic and ethoxylated nonionic surfactants in the range from about 12% to about 50%, preferably from about 14% to about 30%.
• the polydimethylsiloxane component preferably comprises, in total, from'about 0.05% to about 0.75%, more preferably from about 0.3% to about 0.5% by weight of detergent composition and from about 1% to about 30%, more preferably from about 3% to about 12% by weight of additive composition; while the hydrophobic silica component preferably comprises, in total, from about 0.003% to about 0.045%, more preferably from about 0.008% to about 0.025%, by weight of detergent composition and from about 0.05% to about 1%, more preferably from about 0.1% to about 0.5%, by weight of additive composition.
• the weight ratio of total polydimethylsiloxane: total hydrophobic silica preferably lies in the range from about 3:1 to about 100:1, more preferably from about 10:1 to about 60:1.
• the detergent compositions of the invention are preferably made by forming dispersion (a) as a fluid high shear mixture of polydimethylsiloxane in the first nonionic surfactant, forming dispersion (b) as a particulate mixture of hydrophobic silica in the organic carrier, spraying dispersion (a) in fluent form onto a detergent base powder composition, and finally dry mixing dispersion (b) in powder form.
• a suitable base powder composition comprises anionic surfactant and detergency builder in amounts such that the final detergent composition contains from about 30% to about 99% base powder, from about 3% to about 30% anionic surfactant and from about 5% to abut 96% detergency builder.
• Dispersion (b) can be rendered in powder form by agglomerating a molten mix of the dispersion with an inorganic salt in, for example, a pan agglomerator, fluidized bed, Schugi mixer or the like.
• a preferred inorganic salt is sodium tripolyphosphate.
• the particle size of the resulting agglomerate is preferably from about 0.5mm to 2mm, especially from about 0.84 to 1.4mm.
• dispersion (b) can be rendered in powder form by extrusion.
• the nonionic surfactant component of dispersion (a) and the organic carrier of dispersion (b) have melting points in the ranges from 5°C to 36°C, preferably from about 7°C to about 32°C, and from 38°C to 90°C, preferably from 40°C to 55°C respectively.
• the melting point is taken to refer to the temperature at which melting is completed. Conveniently, this temperature can be determined by thermal analysis using a Dupont 910 Differential Scanning Calorimeter with Mechanical Cooling Accessory and R90 Thermal Analyser as follows. A 5-10 mg sample of the material containing no free water or solvent, is encapsulated in a hermetically sealed pan with an empty pan as reference.
• the sample is initially heated until molten and then rapidly cooled (at about 20-30°C/min) to -70°C.
• Thermal analysis is then carried out at a heating rate of 10°C/min using sufficient amplification of ⁇ T signal (ie temperature difference between sample and reference - vertical axis) to obtain an endotherm-peak signal:baseline noise ratio of better than 10:1.
• the melting completion temperature is then the temperature corresponding to the intersection of the tangential line at the steepest part of the endotherm curve at the high temperature end of the endotherm, with the horizontal line, parallel to the sample temperature axis, through the highest temperature endotherm peak.
• the organic carrier component of dispersion (b) can also be defined by the temperature at which onset of melting occurs.
• the melting onset temperature is at least about 36°C, more preferably at least about 38°C.
• the melting onset temperature can once again be determined by thermal analysis as described above and is taken to be the sample temperature at the point of intersection of the base line with a tangent to the steepest part of the endotherm nearest the low temperature end of the endotherm.
• the nonionic surfactants suitable for use in dispersion (a) are condensates of ethylene oxide with a hydrophobic moiety providing a surfactant having an average hydrophilic-lipophilic balance (HLB) in the range from 9 to 13, preferably from about 10 to about 12.5.
• HLB hydrophilic-lipophilic balance
• the hydrophobic moiety may be aliphatic or aromatic in nature and the length of the polyoxyethylene group which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
• Suitable nonionic surfactants include:
• the compounds formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol generally falls in the range of about 1500 to 1800.
• Such synthetic nonionic detergents are available on the market under the Trade Name of "Pluronic" supplied by Wyandotte Chemicals Corporation.
• Especially preferred nonionic surfactants for use in dispersion (a) are the C 9 -C 15 primary alcohol ethoxylates containing 3-S moles of ethylene oxide per mole of alcohol, particularly the C 12 -C 15 primary alcohols containing 6-8 moles of ethylene oxide per mole of alcohol.
• the organic carrier component of dispersion (b) is preferably also based on an ethoxylated nonionic surfactant, but one having an average HLB in the range from about 13.5 to about 19, preferably from about 15 to about 17.5 and having a melting point in the range from about 38°C to about 60° C , preferably from about 40°C to about 55°C.
• Suitable nonionic surfactants are the condensation products of the primary or secondary alcohols having from about 15 to about 24 carbon atoms, in either straight chain or branched chain configuration, with from about 14 to about 100, preferably from about 20 to about 40 moles of ethylene oxide per mole of aliphatic alcohol.
• surfactants of this type are the condensation products of hardened tallow alcohol with an average of between about 20 and about 40 moles, preferably about 25 moles of ethylene oxide per mole of alcohol, the tallow portion comprising essentially between 16 and 22 carbon atoms.
• the polydimethylsiloxane foam controlling agent used herein are high molecular weight polymers having a molecular weight in the range from about 200 to about 200,000, and having a kinematic viscosity in the range from about 20 to 2,000,000 mm 2 /s, preferably from about 500 to to about 50 ,000 mm 2 /s, more preferably from about 3,000 to about 30 , 00 0 mm 2 /s at 25°C.
• the siloxane polymer is generally end-blocked either with trimethylsilyl or hydroxyl groups but other end-blocking groups are also suitable.
• the polymer can be prepared by various techniques such as the hydrolysis and subsequent condensation of dimethyldihalosilanes, or by the cracking and subsequent condensation of dimethylcyclosiloxanes.
• the hydrophobic silica foam controlling agent employed in the present composition preferably has a particle size of not more than about 100 millimicrons and a specific surface area in excess of about 50 m 2 /g. Highly preferred materials have a particle size from about 10 millimicrons to about 20 millimicrons.
• the hydrophobic silica can be made, for example, by reacting fumed silica with a trialkyl chlorosilane (i.e., "silanated") to affix hydrophobic trialkylsilane groups on the surface of the silica. In a preferred and well known process, fumed silica is contacted with trimethylchlorosilanes.
• Combinations of silicone and silica can also be used, both in dispersion (a) and in dispersion (b).
• Such combinations of silicone and silica can be prepared by affixing the silicone to the surface of silica for example by means of the catalytic reaction disclosed in US Patent 3,235,509.
• Suds controlling agents comprising mixtures of silicone and silica prepared in this manner preferably comprise, in dispersion (a), silicone and silica in a silicone:silica ratio of from about 20:1 to about 200:1, more preferably about 25:1 to about 100:1.
• the silica can be chemically and/or physically bound to the silicone in an amount which is preferably about 0.5% to 5% by weight, based on the silicone.
• mixed silicone/silica foam controlling agents can have a silicone:silica ratio of from about 1:1 to about 60:1, preferably from about 10:1 to about 50:1.
• a preferred foam-controlling mixture herein comprises a hydrophobic silanated (most preferably trimethylsilanated) silica having a particle size in the range from about 10 millimicrons to 20 millimicrons and a specific surface area above about 50 m 2 /g intimately mixed with a dimethyl silicone fluid having a molecular weight in the range of from about 500 to about 200,000.
• a hydrophobic silanated (most preferably trimethylsilanated) silica having a particle size in the range from about 10 millimicrons to 20 millimicrons and a specific surface area above about 50 m 2 /g intimately mixed with a dimethyl silicone fluid having a molecular weight in the range of from about 500 to about 200,000.
• foam-controlling mixture suitable herein comprises polydimethylsiloxane fluid, a silicone resin and silica.
• the silicone "resins” used in such compositions can be any alkylated silicone resins, but are usually those prepared from methylsilanes. Silicone resins are commonly described as "three-dimensional" polymers prepared from the hydrolysis of dichlorosilanes.
• the silica components of such compositions are the microporous materials such as the fumed silica aerogels and xerogels having the particle sizes and surface areas herein-above disclosed.
• the siloxane-oxyalkylene copolymer dispersing agent suitable for use herein has the general formula I: wherein a is 0 or an integer from 1 to about 3, R is an alkyl group containing from 1 to about 30 carbon atoms, or a group of formula II: wherein R' is an alkylene group containing from 1 to about 6 carbon atoms, b has a value of from 1 to about 100, preferably from 10 to 30; and R" is a capping group which can be selected from hydrogen, alkyl, acyl, aryl, alkaryl, aralkyl or alkenyl groups containing up to about 20 carbon atoms, sulfate, sulfonate, phosphate, carboxylate, phosphonate, borate or isocyanate groups, or mixtures thereof; Y is a group having the formula III:- wherein R is as defined above and c has a value from 1 to about 200; and wherein at least one R group in the compound has the formula II
• Preferred dispersing agents of the above type are selected from copolymers having the general formulae I V to VII: . wherein R''' is a C 1-10 alkyl group, Me is methyl, G is the group of formula II, a has a value of 0 or 1, p has a value of at least 1, q has a value of 0 to about 50 and r has a value of 1 to about 50.
• Preferred dispersants contain G groups in non-terminal positions and contain a mixture of oxyethylene and oxypropylene groups, particularly in about a 1:1 ratio. Highly preferred are dispersants of formula VI I having p+r from about 30 to about 120 with the ratio p:r from about 2:1 to about 8:1.
• Suitable microcrystalline waxes for inclusion in dispersion (b) have a melting point in the range from about 35°C-115°C, preferably from about 65°C to about 100°C, a saponification value of less than 100, a molecular weight in the range 400-1000, and a penetration value of at . least 6, measured at 77°C by ASTM-D1321.
• Suitable examples include microcrystalline and oxidised microcrystalline waxes; Fischer-Tropsch and oxidised Fischer-Tropsch waxes; ozokerite, ceresin, montan wax, beeswax, candellila and carnauba wax.
• compositions of the invention can be supplemented by all manner of detergent components.
• a highly preferred additional component is from about 3% to about 30% of anionic surfactant.
• the anionic surfactant may be any one or more of the materials used conventionally in laundry detergents.
• Suitable synthetic anionic surfactants are water-soluble salts of alkyl benzene sulphonates, alkyl sulphates, alkyl polyethoxy ether sulphates, paraffin sulphonates, alpha-olefin sulphonates, alpha-sulpho-carboxylates and their esters, alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, alkyl phenol polyethoxy ether sulphates, 2-acyloxy alkane-I-sulphonate, and beta-alkyloxy alkane sulphonate.
• a particularly suitable class of anionic surfactants includes water-soluble salts, particularly the alkali metal, ammonium and alkanolammonium salts or organic sulphuric reaction products having in their molecular structure an alkyl or alkaryl group containing from about 8 to about 22, especially from about 10 to about 20 carbon atoms and a sulphonic acid or sulphuric acid ester group.
• alkyl is the alkyl portion of acyl groups.
• Examples of this group of synthetic detergents which form part of the detergent compositions of the present invention are the sodium and potassium alkyl sulphates, especially those obtained by sulphating the higher alcohols (C 8-18 ) carbon atoms produced by reducing the glycerides .
• alkyl group contains from about 9 to about 15, especially about 11 to about 13, carbon atoms, in straight chain or branched chain configuration, e.g. those of the type described in U.S.P. 2,220,099 and 2,477,383 and those prepared from alkylbenzenes obtained by alkylation with straight chain chloroparaffins (using aluminium trichloride catalysis) or straight chain olefins (using hydrogen fluoride catalysis).
• straight chain alkyl benzene sulphonates in which the average of the alkyl group is about 11.8 carbon atoms, abbreviated as C 11 . 8 LAS.
• anionic detergent compounds herein include the sodium C 10-18 alkyl glyceryl ether sulphonates, especially those ethers of higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulphonates and sulphates; and sodium or potassium salts of alkyl phenol ethylene oxide ether sulphate containing about 1 to about 10 units of ethylene oxide per molecule and wherein the alkyl groups contain about 8 to about 12 carbon atoms.
• Other useful anionic detergent compounds herein include the water-soluble salts or esters of ⁇ -sulphonated fatty acids containing from about 6 to 20 carbon atoms in the fatty acid group and from about 1 to 10 carbon atoms in the ester group; water-soluble salts of 2-acyloxy-alkane-l-sulphonic acids containing from about 2 to 9 carbon atoms in the acyl group and from about 9 to about 23 carbon atoms in the alkane moiety; alkyl ether sulphates containing from about 10 to 18, especially about 12 to 16, carbon atoms in the alkyl group and from about 1 to 12, especially 1 to 6, more especially 1 to 4 moles of ethylene oxide; water-soluble salts of olefin sulphonates containing from about 12 to 24, preferably aout 14 to 16, carbon atoms, especially those made by reaction with sulphur trioxide followed by neutralization under conditions such that any sultones present are hydrolysed to the corresponding hydroxy alkane sulphonates
• alkane chains of the foregoing non-soap anionic surfactants can be derived from natural sources such as coconut oil or tallow, or can be made synthetically as for example using the Ziegler or Oxo processes. Water solubility can be achieved by using alkali metal, ammonium or alkanolammonium cations; sodium is preferred. Suitable fatty acid soaps can be selected from the ordinary alkali metal (sodium, potassium), ammonium, and alkylolammonium salts of higher fatty acids containing from about 8 to about 24, preferably from about 10 to about 22 and especially from about 16 to about 22 carbon atoms in the alkyl chain.
• Suitable fatty acids can be obtained from natural sources such as, for instance, from soybean oil, castor oil, tallow, whale and fish oils, grease, lard and mixtures thereof).
• the fatty acids also can be synthetically prepared (e.g., by the oxidation of petroleum, or by hydrogenation of carbon monoxide by the Fischer-Tropsch process).
• Resin acids are suitable such as rosin and those resin acids in tall oil.
• Napthenic acids are also suitable.
• Sodium and potassium soaps can be made by direct saponification of the fats and oils or by the neutralization of the free fatty acids which are prepared in a separate manufacturing process. Particularly useful are the sodium and potassium salts of the mixtures of fatty acids derived from tallow and hydrogenated fish oil.
• Mixtures of anionic surfactants are particularly suitable herein, especially mixtures of sulfonate and sulfate surfactants in a weight ratio of from about 5:1 to about 1:5, preferably from about 5:1 to about 1:1, more preferably from about 5:1 to about 1.5:1.
• an alkyl benzene sulfonate having from 9 to 15, especially 11 to 13 carbon atoms in the alkyl radical, the cation being an alkali metal preferably sodium; and either an alkyl sulfate having from 10 to 20, preferably 12 to 18 carbon atoms in the alkyl radical or an ethoxy sulfate having from 10 to 20, preferably 10 to 16 carbon atoms in the alkyl radical and an average degree of ethoxylation of 1 to 6, having an alkali metal cation, preferably sodium.
• detergent compositions of the invention can be supplemented by low levels, preferably up to about 6%, of cosurfactants, especially amine oxides, quaternary ammonium surfactants and mixtures thereof.
• Suitable surfactants of the amine oxide class have the general formula VIII wherein R 1 is a linear or branched alkyl or alkenyl group having 8 to 20 carbon atoms, each R 2 is independently selected from C 1-4 alkyl and -(C n H 2n O) m H where i is an integer from 1 to 6, j it 0 or 1, n is 2 or 3 and m is from 1 to 7, the sum total of C n H 2n O groups in a molecule being no more than 7.
• R 1 has from 10 to 14 carbon atoms and each R 2 is independently selected from methyl and -(C H 2n O) m H wherein m is from 1 to 3 and the sum total of C n H 2n 0 groups in a molecule is no more than 5, preferably no more than 3.
• j is 0 and each R 2 is methyl, and R 1 is C12-C14 alkyl.
• Another suitable class of amine oxide species is represented by bis-amine oxides having the following substituents.
• Suitable quaternary ammonium surfactants for use in the present composition can be defined by the general formula IX: wherein R 3 is a linear or branched alkyl, alkenyl or alkaryl group having 8 to 16 carbon atoms and each R is independently selected from C 1-4 alkyl, C 1-4 alkaryl and -(C n H 2n O) m wherein i is an integer from 1 to 6, j is 0 or 1, n is 2 or 3 and m is from 1 to 7, the sum total of C n H 2n O groups in a molecule being no more than 7, and wherein Z represents counteranion in number to give electrical neutrality,
• R has from 10 to 14 carbon atoms and each R 4 is independently selected from methyl and (C n H 2n O) m H wherein m is from 1 to 3 and the sum total of C n H 2n O groups in a molecule is no more than 5, preferably no more than 3..
• j is 0, R 4 is selected from methyl, hydroxyethyl and hydroxypropyl and R 3 is C 12 -C 14 alkyl.
• Particularly preferred surfactants of this class include C 12 alkyl trimethylammonium salts, C 14 alkyltrimethylammonium salts, coconutalkyltrimethylammonium salts, coconutalkyldimethyl- hydroxyethylammonium salts, coconutalkyldimethylhydroxy- propylammonium salts, and C 12 alkyldihydroxyethylmethyl ammonium salts.
• Another group of useful cationic compounds are the diammonium salts of formula II in which j is 1, R 3 is C 12 -C 14 alkyl, each R 4 is methyl, hydroxyethyl or hydroxypropyl and i is 2 or 3.
• R 3 is coconut alkyl
• R 4 is methyl
• i is 3.
• Detergent compositions of the invention can also include at least one detergent organic or inorganic builder salt which can be any one of the water soluble or water insoluble salts conventionally used for this purpose.
• Suitable inorganic builder salts include orthophosphates, pyrophosphates, tripolyphosphates and the higher polymeric glassy phosphates, silicates, carbonates, and the water insoluble crystalline aluminosilicates such as hydrated Zeolite A, X or P.
• Organic builder salts include the aminocarboxylates such as the salts of nitrilotriacetic acid (NTA), ethylenediaminetetra acetic acid (EDTA) and diethylenetriaminepenta acetic acid (D ET PA) and the methylene phosphonate analogues of these materials nitrilotrimethylene-phosphonic acid (NT M P), ethylendiaminetetramethylenephosphonic acid (EDTMP) and diethylenetriaminepentamethylenephosphonic acid (DETPMP), as well as the salts of polycarboxylic acids such as lactic acid, glycollic acid and ether derivatives thereof as disclosed in Belgian Patents 821,368, 821,369 and 821,370; succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycollic acid, tartaric acid, tartronic acid and fumaric acid; citric acid, aconitic acid, citraconic acid, carboxymethyloxys
• the builder salts preferably comprise from about 5% to about 96% by weight of the composition, preferably from about 10% to about 50% by weight for granular detergents, and preferably from about 5% to about 20% for liquid detergents.
• compositions of the present invention can be supplemented by all manner of detergent components.
• Soil suspending agents at about 0.1% to 10% by weight such as water-soluble salts of carboxymethyl-cellulose, carboxyhydroxymethyl cellulose, and polyethylene glycols having a molecular weight of about 400 to 10,000 are common components of the present invention.
• Dyes, pigments, optical brighteners, and perfumes can be added in varying amounts as desired.
• Enzymes suitable for use herein include those discussed in U.S. patents 3,519,570 and 3,533,139 to McCarty and McCarty et al issued July 7 1970 and January 5, 1971 respectively.
• alkali metal, or alkaline earth metal, silicate can also be present.
• the alkali metal silicate preferably is used in an amount from 0.5% to 10% preferably from 3% to 8%.
• Suitable silicate solids have a molar ratio of Si02/alkali metal 2 0 in the range from about 0.5-to about 4.0, but much more preferably from 1.0 to 1.8, especially about 1.6.
• the alkali metal silicates suitable herein can be commercial preparations of the combination of silicon dioxide and alkali metal oxide, fused together in varying proportions.
• Granular detergent compositions herein can also advantageously contain a peroxy bleaching component in an amount from about 3% to about 40% by weight, preferably from about 8% to about 33% by weight.
• suitable peroxy bleach components for use herein include perborates, persulfates, persilicates, perphosphates, percarbonates, and more generally all inorganic and organic peroxy bleaching agents which are known to be adapted for use in the subject compositions.
• the composition can also advantageously include a bleach activator which is normally an organic compound containing and N-acyl, or an O-acyl (preferably acetyl.) group.
• Preferred materials are N,N,N',N'-tetraacetyl ethylene diamine and N,N,N',N'-tetraacetylglycouril.
• the bleach activator is preferably added at a level from 0.5% to 5% by weight of composition.
• a further preferred ingredient of the instant compositions is from about 0.01 to about 4%, especially from about 0.1 to about 1.0% by weight of a polyphosphonic acid or salt thereof which is found to provide bleachable stain detergency benefits.
• Especially preferred polyphosphonates have the formula X:- wheren each R is CH 2 P0 3 H 2 or a water-soluble salt thereof and n is from 0 to 2.
• Examples of compounds within this class are aminotri(methylenephosphonic acid), ethylene diaminetetra(methylenephosphonic acid) and diethylene triaminepenta(methylenephosphonic acid). Of these, ethylerediaminetetra(methylenephosphonic acid) is particularly preferred.
• a further optional component is from about 0.1% to about 3%, especially from about 0.25% to about 1.5% of a polymeric material having a molecular weight of from about 2000 to about 2,000,000 and which is a copolymer of maleic acid or anhydride and a polymerisable monomer selected from C 1 -C 12 alkyl vinyl ethers, acrylic and methacrylic acid and C 1 -C 20 esters thereof, alkenes having from 2 to 12 carbon atoms, N-vinyl pyrrolidone and styrene.
• carboxylates are 1:1 styrene/maleic acid copolymer, di-isobutylene/maleic acid copolymers, methyl vinyl ether/ maleic acid copolymers of molecular weight from about 50,000 to about 300,000, and 1:1 to 1:4 maleic acid/acrylic acid copolymers of molecular weight from about 12,000 to about 100,000.
• suitable polycarboxylates are poly-fl-hydroxy acrylates and lactones thereof as described in Belgian Patent 817,678 and British Patent 1,425,307.
• Another suitable component of the present compositions is a water-soluble magnesium salt which is added at levels in the range from about 0.015% to about 0.2%, preferably from about 0.03% to about 0.15% and more preferably from about 0.05% to about 0.12% by weight of the compositions (based on weight of magnesium).
• Suitable magnesium salts include magnesium sulfate, magnesium sulfate heptahydrate, magnesium chloride, magnesium chloride hexahydrate, magnesium fluoride and magnesium acetate.
• the magnesium salt is added to granular compositions as part of the aqueous slurry crutcher mix and is then converted to dry granular form, for instance by spray drying.
• Liquid detergent compositions of the invention can additionally be supplemented by pH regulators such as potassium hydroxide, potassium carbonate, potassium bicarbonate, sodium hydroxide, sodium carbonate, sodium bicarbonate, and mono-, di- and triethanolamine; solvents such as ethyl alcohol, isopropanol, propylene glycol, propane-1, 2-diol, hexyleneglycol; and hydrotropes such as urea.
• pH regulators such as potassium hydroxide, potassium carbonate, potassium bicarbonate, sodium hydroxide, sodium carbonate, sodium bicarbonate, and mono-, di- and triethanolamine
• solvents such as ethyl alcohol, isopropanol, propylene glycol, propane-1, 2-diol, hexyleneglycol
• hydrotropes such as urea.
• Granular detergent compositions of the invention are preferably prepared by spray-drying an aqueous slurry comprising the anionic surfactant and detergency builder.
• the aqueous slurry is mixed at a temperature in the range from about 70-90°C and the water-content of the slurry adjusted to a range of about 25% to about 45%, preferably about 30% to about 38% by weight.
• Spray drying is undertaken with a drying gas inlet temperature of from about 250-350°C, preferably about 275-330°C, providing a final moisture content in the range of from about 8% to 14% by weight.
• the dispersion (a) is sprayed in fluid form onto the spray-dried detergent granules and finally dispersion (b) is dry mixed in the composition in powder form.
• the granular compositions of the invention can also be prepared in concentrated form with a bulk density greater than about 600 g/litre.
• a preferred process for preparing a concentrated granule comprises the steps of:
• Granular detergent compositions are prepared as follows.
• a base powder composition is first prepared by mixing the indicated components in a crutcher as an aqueous slurry at a temperature of about 80°C and containing about 35% water. The slurry is then spray dried at a gas inlet temperature of about 300°C to form base powder granules.
• Additive dispersion (a) is then prepared as a molten mixture of the nonionic surfactant, foam-controlling agent and dispersing agent and the mixture is subjected to high shear mixing.
• Additive dispersion (b) is then formed by dispersing foam controlling agent in molten organic carrier and the dispersion is sprayed onto sodium tripolyphosphate in a fluidized bed.
• the base powder composition is dry mixed with additive dispersion (b), enzyme-and bleach components, and additive dispersion (a) is sprayed onto the total mixture.
• the above products combine superior detergency performance together with excellent foam regulation characteristics across the range of wash temperature, product usage, soil, load and rinsing conditions, even after prolonged storage under warm humid conditions.

Landscapes

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

Applications Claiming Priority (2)

Publications (2)

Family

ID=10529658

Family Applications (1)

Country Status (2)

Cited By (20)

Citations (5)

• 1983
  • 1983-04-08 DE DE8383301989T patent/DE3373918D1/de not_active Expired
  • 1983-04-08 EP EP19830301989 patent/EP0091802B1/de not_active Expired

Patent Citations (5)

Also Published As

Similar Documents

Legal Events