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WO1992006160A1 - Systemes tensioactifs non ioniques contenant des amides d'acides gras de polyhydroxy et un ou plusieurs tensioactifs non ioniques supplementaires - Google Patents

Systemes tensioactifs non ioniques contenant des amides d'acides gras de polyhydroxy et un ou plusieurs tensioactifs non ioniques supplementaires Download PDF

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Publication number
WO1992006160A1
WO1992006160A1 PCT/US1991/006980 US9106980W WO9206160A1 WO 1992006160 A1 WO1992006160 A1 WO 1992006160A1 US 9106980 W US9106980 W US 9106980W WO 9206160 A1 WO9206160 A1 WO 9206160A1
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WIPO (PCT)
Prior art keywords
nonionic surfactant
fatty acid
alkyl
polyhydroxy fatty
surfactants
Prior art date
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PCT/US1991/006980
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English (en)
Inventor
Jerome Howard Collins
Bruce Prentiss Murch
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The Procter & Gamble Company
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Filing date
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Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to DE69127449T priority Critical patent/DE69127449T2/de
Priority to SK24493A priority patent/SK24493A3/sk
Priority to AU86469/91A priority patent/AU664356B2/en
Priority to EP91917564A priority patent/EP0550606B1/fr
Priority to CS93432A priority patent/CZ43293A3/cs
Priority to BR919106934A priority patent/BR9106934A/pt
Priority to JP03516294A priority patent/JP3119873B2/ja
Publication of WO1992006160A1 publication Critical patent/WO1992006160A1/fr
Priority to NO93931019A priority patent/NO931019L/no
Priority to FI931360A priority patent/FI931360A/fi

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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
    • C11D1/66—Non-ionic compounds
    • C11D1/835—Mixtures of non-ionic with cationic 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
    • C11D1/38—Cationic compounds
    • C11D1/52—Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/525—Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest
    • 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
    • C11D1/662—Carbohydrates or derivatives
    • 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

Definitions

  • the stain-removing performance of detergent compositions is improved through the use of a nonionic surfactant system compris ⁇ ing one or more polyhydroxy fatty acid amides and one or more additional nonionic surfactants.
  • laundry detergent compositions can be formulated in a number of different ways to address a number of different laundering problems.
  • such detergent compositions may contain builders, optical brighteners, dispersants, etc., to address various cleaning problems encountered in laundering operations.
  • consumers need detergent compositions which are effective against the broadest possible spectrum of stains and soils.
  • Detergent for ulators address this need by providing detergent compositions containing mixed surfactants which are broadly effective in their cleaning performance.
  • the present invention provides nonionic surfactant systems which comprise one or more polyhydroxy fatty acid amides and one or more additional nonionic surfactants.
  • the present invention also provides laundry detergent compositions which contain these nonionic surfactant systems. When included in such laundry detergent compositions, these nonionic surfactant systems unex ⁇ pectedly improve the effectiveness of such compositions against greasy/oily stains across a broad range of laundry conditions.
  • BACKGROUND ART A variety of polyhydroxy fatty acid amides have been described in the art. N-acyl, N-methyl glucamides, for example, are disclosed by J. W. Goodby, M. A. Marcus, E. Chin, and P. L.
  • N-alkyl glucamides in detergent compositions has also been discussed.
  • U.S. Patent 2,965,576, issued December 20, 1960 to E. R. Wilson, and G.B. Patent 809,060, published February 18, 1959, assigned to Thomas Hedley & Co., Ltd. relate to deter ⁇ gent compositions containing anionic surfactants and certain amide surfactants, which can include N-methyl glucamide, added as a low temperature suds enhancing agent.
  • These compounds include an N-acyl radical of a higher straight chain fatty acid having 10-14 carbon atoms.
  • These compositions may also contain auxiliary materials such as alkali metal phosphates, alkali metal silicates, sulfates, and carbonates. It is also generally indicated that additional constituents to impart desirable properties to the composition can also be included in the compositions, such as fluorescent dyes, bleaching agents, perfumes, etc.
  • U.S. Patent 2,703,798, issued March 8, 1955 to A. M. Schwartz relates to aqueous detergent compositions containing the condensation reaction product of N-alkyl glucamine and an ali ⁇ phatic ester of a fatty acid.
  • the product of this reaction is said to be useable in aqueous detergent compositions without further purification.
  • PCT International Application WO 83/04412 published December 22, 1983, by J.
  • Hildreth relates to amphiphilic compounds containing polyhydroxyl aliphatic groups said to be useful for a variety of purposes including use as surfactants in cosmetics, 5 drugs, shampoos, lotions, and eye ointments, as emulsifiers and dispensing agents for medicines, and in biochemistry for solubilizing membranes, whole cells, or other tissue samples, and for preparing of liposo es.
  • Included in this disclosure are compounds of the formula R'C0N(R)CH2R" and R"C0N(R)R' wherein R is 10 hydrogen or an organic grouping, R " is an aliphatic hydrocarbon group of at least three carbon atoms, and R" is the residue of an aldose.
  • fatty acid amides as thickening agents in aqueous detergent systems. Included are amides of the formula RjC(0)N(X)R2 wherein Rl is a C ⁇ Ci7 (preferably C7-C17) alkyl, R2 is hydrogen, a C1-C18 (preferably Ci-C ⁇ ) alkyl, or an alkylene oxide, and X is a polyhydroxy alkyl having four to seven carbon atoms, e.g., 0 N-methyl, coconut fatty acid glucamide.
  • the thickening properties of the amides are indicated as being of particular use in liquid surfactant systems containing paraffin sulfonate, although the aqueous surfactant systems can contain other anionic surfactants, such as alkylaryl sulfonates, olefin sulfonate, sulfosuccinic acid ⁇ half ester salts, and fatty alcohol ether sulfonates, and nonionic surfactants such as fatty alcohol polyglycol ether, alkylphenol polyglycol ether, fatty acid polyglycol ester, polypropylene oxide-polyethylene oxide mixed polymers, etc.
  • anionic surfactants such as alkylaryl sulfonates, olefin sulfonate, sulfosuccinic acid ⁇ half ester salts, and fatty alcohol ether sulfonates
  • nonionic surfactants such as fatty alcohol polyglycol ether, alkylphenol polygly
  • Paraffin sulfonate/ N-methyl coconut fatty acid gluca ide/nonionic surfactant shampoo 0 formulations are exemplified.
  • the N-polyhydroxy alkyl fatty acid amides are said to have superior skin tolerance attributes.
  • U.S. Patent 2,982,737 issued May 2, 1961, to Boettner, et al., relates to detergent bars containing urea, sodium lauryl sulfate anionic surfactant, and an N-alkylglucamide nonionic surfactant which is selected from N-methyl ,N-sorbityl lauramide and N-methyl, N-sorbityl myristamide.
  • N-alkylglucamide nonionic surfactant which is selected from N-methyl ,N-sorbityl lauramide and N-methyl, N-sorbityl myristamide.
  • Other glucamide surfactants are disclosed, for example, in DT 2,226,872, published December 20, 1973, H. W.
  • Eckert, et al. which relates to washing compositions comprising one or more surfactants and builder salts selected from polymeric phosphates, sequestering agents, and washing alkalis, improved by the addition of an N-acylpolyhydroxyalkyl-amine of the formula R ⁇ C(0)N(R2)CH2- (CH0H) n CH20H, wherein Ri is a C1-C3 alkyl, R2 is a C10-C22 alkyl, and n is 3 or 4.
  • the N-acylpolyhydroxyalkyl-amine is added as a soil suspending agent.
  • Eckert, et al. relates to detergent compositions comprising at least one surfactant selected from the group of anionic, zwitterionic, and nonionic surfactants and, as a textile softener, an N-acyl, N-alkyl polyhydroxylalkyl compound of the formula R ⁇ N(Z)C(0)R2 wherein Rj is a 10-C22 alkyl, R2 is a C7-C21 alkyl, Ri and R2 total from 23 to 39 carbon atoms, and Z is a polyhydroxyalkyl which can be -CH2(CHOH) m CH2 ⁇ H where m is 3 or 4.
  • U.S. Patent 4,021,539 issued May 3, 1977, to H. M ⁇ ller, et al., relates to skin treating cosmetic compositions containing N-polyhydroxylalkyl-amines which include compounds of the formula RlN(R)CH(CH0H) m R2 wherein Ri is H, lower alkyl, hydroxy-lower alkyl, or aminoalkyl, as well as heterocyclic aminoalkyl, R is the same as Ri but both cannot be H, and R2 is CH2OH or COOH.
  • French Patent 1,360,018, April 26, 1963 assigned to Commer- cial Solvents Corporation, relates to solutions of formaldehyde stabilized against polymerization with the addition of amides of the formula RC(0)N(R ⁇ )G wherein R is a carboxylic acid functional ⁇ ity having at least seven carbon atoms, Ri is hydrogen or a lower alkyl group, and G is a glycitol radical with at least 5 carbon atoms.
  • German Patent 1,261,861, February 29, 1968, A. Heins relates to glucamine derivatives useful as wetting and dispersing agents of the formula N(R)(R ⁇ )(R2) wherein R is a sugar residue of glucamine, Rj is a C10-C20 a1k y ⁇ radical, and R2 is a C1-C5 acyl radical .
  • G.B. Patent 745,036, published February 15, 1956, assigned to Atlas Powder Company, relates to heterocyclic amides and carbox ⁇ ylic esters thereof that are said to be useful as chemical intermediates, emulsifiers, netting and dispersing agents, deter ⁇ gents, textile softeners, etc.
  • the compounds are expressed by the formula N(R)(R ⁇ )C(0)R2 wherein R is the residue of an anhydrized hexane pentol or a carboxylic acid ester thereof, Ri is a mono- valent hydrocarbon radical, and -C(0)R2 is the acyl radical of a carboxylic acid having from 2 to 25 carbon atoms.
  • U.S. Patent 3,312,627 discloses solid toilet bars that are substantially free of anionic detergents and alkaline builder materials, and which contain lithium soap of certain fatty acids, a nonionic surfactant selected from certain propylene oxide-ethylenediamine-ethylene oxide condensates, propylene oxide-propylene glycol-ethylene oxide condensates, and polymerized ethylene glycol, and also contain a nonionic lathering component which can include polyhydroxyamide of the formula RC(0)NR 1 (R 2 ) wherein RC(0) contains from about 10 to about 14 carbon atoms, and R 1 and R 2 each are H or Ci-C ⁇ alkyl groups, said alkyl groups containing a total number of carbon atoms of from 2 to about 7 and a total number of substituent hydroxyl groups of from 2 to about 6.
  • RC(0)NR 1 (R 2 ) wherein RC(0) contains from about 10 to about 14 carbon atoms, and R 1 and R 2 each are H or Ci-C ⁇ alkyl groups, said
  • Rl is H, a C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or mixtures thereof, R 2 is a C5-C31 hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyl groups directly connected to the chain, or an alkoxylated derivative thereof; and
  • the present invention also provides laundry detergent compositions which contain the nonionic surfactant systems described above. When included in such laundry detergent compositions, these nonionic surfactant systems unexpectedly improve the stain removal performance of such compositions against greasy/oily stains across a broad range of laundry conditions.
  • This invention further provides a method for improving the stain-removing performance of detergent compositions by incorporating into such compositions the nonionic surfactant systems described above.
  • the nonionic surfactant systems of the present invention comprise one or more polyhydroxy fatty acid amides and one or more additional nonionic surfactants.
  • the weight ratio of polyhydroxy fatty acid amides to additional nonionic surfactants is in the range of from about 1:5 to about 5:1, preferably from about 1:3 to about 3:1, more preferably from about 1:1.5 to about 1.5:1.
  • the components of the nonionic surfactant systems of the present invention are set forth below.
  • the polyhydroxy fatty acid amide surfactant component of the present invention comprises compounds of the structural formula: 0 R l
  • Rl is H, C1-C4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof, preferably C1-C4 alkyl, more preferably Ci or C2 alkyl, most preferably Ci alkyl (i.e., methyl); and R 2 is a C5-C31 hydrocarbyl, preferably straight chain C7-C19 alkyl or alkenyl, more preferably straight chain C9-C17 alkyl or alkenyl, most preferably straight chain C11-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
  • Z preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z is a glycityl.
  • Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose, and xylose.
  • high dextrose corn syrup, high fructose corn syrup, and high maltose corn syrup can be utilized as well as the individual sugars listed above. These corn syrups may yield a mix of sugar components for Z. It should be understood that it is by no means intended to exclude other suitable raw materials.
  • Z preferably will be selected from the group consisting of -CH 2 -(CH0H) n -CH 2 0H, -CH(CH 2 0H)-(CH0H) n . 1 -
  • n is an integer from 3 to 5, inclusive
  • R' is H or a cyclic or aliphatic onosac- charide, and alkoxylated derivatives thereof.
  • Most preferred are glycityls wherein n is 4, particularly -CH2-(CHOH)4-CH2 ⁇ H.
  • R can be, for example, N-methyl, N-ethyl, N-propyl, N-isopropyl, N-butyl, N-2-hydroxy ethyl, or N-2-hydroxy propyl .
  • R 2 -C0-N ⁇ can be, for example, coca ide, steara ide, oleamide, laura ide, yristamide, caprica ide, palmitamide, tallowamide, etc.
  • Z can be 1-deoxyglucityl, 2-deoxyfructityl , 1-deoxymaltityl, 1-deoxylactityl , 1-deoxygalactityl, 1-deoxymannityl, 1-deoxymalto- triotityl, etc.
  • the most preferred polyhydroxy fatty acid amide has the general formula
  • R 2 is a C11-C17 straight-chain alkyl or alkenyl group.
  • polyhydroxy fatty acid amides are known in the art. In general, they can be made by reacting an alkyl amine with a reducing sugar in a reductive amination reaction to form a corresponding N-alkyl polyhydroxyamine, and then reacting the N-alkyl polyhydroxyamine with a fatty aliphatic ester or triglyceride in a condensation/amidation step to form the N-alkyl, N-polyhydroxy fatty acid amide product.
  • Processes for making compositions containing polyhydroxy fatty acid amides are disclosed, for example, in G.B. Patent Specification 809,060, published February 18, 1959, by Thomas Hedley & Co., Ltd., U.S.
  • N-deoxyglycityl fatty acid amides wherein the glycityl component is derived from glucose and the N-alkyl or N-hydroxyalkyl functionality is N-methyl, N-ethyl, N-propyl, N-butyl, N-hydroxyethyl , or N-hydroxypropyl
  • the product is made by reacting N-alkyl- or N-hydroxyalkyl-glucamine with a fatty ester selected from fatty methyl esters, fatty ethyl esters, and fatty triglycerides in the presence of a catalyst selected from the group consisting of trilithium phosphate, trisodium phosphate, tripotassium phosphate, tetrasodium pyrophosphate, pentapotassium tripolyphosphate, lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide, lithium carbonate, sodium carbonate, potassium carbonate
  • the amount of catalyst is preferably from about 0.5 mole % to about 50 mole %, more preferably from about 2.0 mole % to about 10 mole %, on an N-alkyl or N-hydroxyalkyl-glucamine molar basis.
  • the reaction is preferably carried out at from about 138 ⁇ C to about 170"C for typically from about 20 to about 90 minutes.
  • the reaction is also preferably carried out using from about 1 to about 10 weight % of a phase transfer agent, calculated on a weight percent basis of total reaction mixture, selected from saturated fatty alcohol polyethoxylates, alkylpolyglycosides, linear glyca ide surfactant, and mixtures thereof.
  • a phase transfer agent calculated on a weight percent basis of total reaction mixture, selected from saturated fatty alcohol polyethoxylates, alkylpolyglycosides, linear glyca ide surfactant, and mixtures thereof.
  • this process is carried out as follows: (a) preheating the fatty ester to about 138 ⁇ C to about 170 ⁇ C; (b) adding the N-alkyl or N-hydroxyalkyl glucamine to the heated fatty acid ester and mixing to the extent needed to form a two-phase liquid/liquid mixture;
  • N-linear glucosyl fatty acid amide product is added to the reaction mixture, by weight of the reactants, as the phase transfer agent if the fatty ester is a
  • polyhydroxy "fatty acid” amide materials used herein also offer the advantages to the detergent formulator that they can be
  • the processes used to produce them 0 will also typically produce quantities of nonvolatile by-product such as esteramides and cyclic polyhydroxy fatty acid amide.
  • the level of these by-products will vary depending upon the particular reactants and process conditions.
  • the polyhydroxy fatty acid amide incorporated into the detergent compositions 5 hereof will be provided in a form such that the polyhydroxy fatty acid amide-containing composition added to the detergent contains less than about 10%, preferably less than about 4%, of cyclic polyhydroxy fatty acid amide.
  • the preferred processes described above are advantageous in that they can yield rather low levels of 0 by-products, including such cyclic amide by-product.
  • the nonionic surfactant systems of the present invention comprise, in addition to the polyhydroxy fatty acid amide component, one or more of the nonionic surfactants described ⁇ herein.
  • the nonionic surfactants described herein will hereinafter be referred to as "additional nonionic surfactants.”
  • additional nonionic surfactants Nonionic compounds other than these additional nonionic surfactants may be optionally included in the nonionic surfactant systems of the present invention.
  • These other, optional nonionic compounds will hereinafter be referred to as “optional nonionics.” Without intending to be limited thereby, it is believed that when such optional nonionics are included in the nonionic surfactant systems of the present invention, they do not provide the unexpected stain-removal benefits already described herein.
  • Polyethylene, polypropylene, and polybutylene oxide conden ⁇ sates of alkyl phenols are suitable for use as the additional nonionic surfacant of the nonionic surfactant systems of the present invention, with the polyethylene oxide condensates being preferred.
  • These compounds include the condensation products of alkyl phenols having an alkyl group containing from about 6 to about 14 carbon atoms, preferably from about 8 to about 14 carbon atoms, in either a straight-chain or branched-chain configuration with the alkylene oxide.
  • the ethylene oxide is present in an amount equal to from about 5 to about 25 moles, more preferably from about 3 to about 15 moles, of ethylene oxide per mole of alkyl phenol.
  • nonionic surfactants of this type include IgepalTM C0-630, marketed by the GAF Corporation; and TritonTM X-45, X-114, X-100, and X-102, all marketed by the Rohm & Haas Company. These surfactants are commonly referred to as alkylphenol alkoxylates (e.g., alkyl phenol ethoxylates).
  • the condensation products of primary and secondary aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide are suitable for use as the additional nonionic surfactant of the nonionic surfactant systems of the present invention.
  • the al yl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms.
  • nonionic surfactants of this type include TergitolTM 15-S-9 (the condensa ⁇ tion product of C11-C15 linear alcohol with 9 moles ethylene oxide), TergitolTM 24-L-6 NMW (the condensation product of C12-C14 primary alcohol with 6 moles ethylene oxide with a narrow molecular weight distribution), both marketed by Union Carbide Corporation; NeodolTM 45-9 (the condensation product of C14-C15 linear alcohol with 9 moles of ethylene oxide), NeodolTM 23-6.5 (the condensation product of C12-C13 linear alcohol with 6.5 moles of ethylene oxide), NeodolTM 45-7 (the condensation product of C14-C15 linear alcohol with 7 moles of ethylene oxide), Neodol TM 45-4 (the condensation product of C14-C15 linear alcohol with 4 moles of ethylene oxide), marketed by Shell Chemical Company, and KyroTM EOB (the condensation product of C13-C15 alcohol with 9 moles ethylene oxide), marketed by The Procter
  • alkylpolysaccharides disclosed in U.S. Patent 4,565,647, Llenado, issued January 21, 1986, having a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g., a polyglycoside, hydrophilic group containing from about 1.3 to about 10, prefer ⁇ ably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
  • Any reducing saccharide containing 5 or 6 carbon atoms can be used, e.g., glucose, galactose and galactosyl moieties can be substituted for the glucosyl moieties.
  • the hydrophobic group is attached at the 2-, 3-, 4-, etc. positions thus giving a glucose or galactose as opposed to a glucoside or galactoside.
  • the intersaccharide bonds can be, e.g., between the one position of the additional saccharide units and the 2-, 3-, 4-, and/or 6- positions on the preceding sacchar ⁇ ide units.
  • a polyalkylene- oxide chain joining the hydrophobic moiety and the polysaccharide moiety.
  • the preferred alkyleneoxide is ethylene oxide.
  • Typical hydrophobic groups include alkyl groups, either saturated or unsaturated, branched or unbranched containing from about 8 to about 18, preferably from about 10 to about 16, carbon atoms.
  • the alkyl group is a straight chain saturated alkyl group.
  • the alkyl group can contain up to about 3 hydroxy groups and/or the polyalkyleneoxide chain can contain up to about 10, preferably less than 5, alkyleneoxide moieties.
  • Suitable alkyl polysaccharides are octyl, nonyldecyl, undecyldodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, and octadecyl, di-, tri-, tetra-, penta-, and hexaglucosides, galactosides, lactos- ides, glucoses, fructosides, fructoses and/or galactoses.
  • Suit- able mixtures include coconut alkyl, di-, tri-, tetra-, and pentaglucosides and tallow alkyl tetra-, penta-, and hexa ⁇ glucosides.
  • the preferred alkylpolyglycosides have the formula R 2 0(C n H 2n O)t(glycosyl) x wherein R 2 is selected from the group consisting of alkyl, alkyl- phenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from about 10 to about 18, prefer ⁇ ably from about 12 to about 14, carbon atoms; n is 2 or 3, prefer ⁇ ably 2; t is from 0 to about 10, preferably 0; and x is from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7.
  • the glycosyl is pre ⁇ ferably derived from glucose.
  • the alcohol or alkylpolyethoxy alcohol is formed first and then reacted with glucose, or a source of glucose, to form the gluco- side (attachment at the 1-position).
  • the additional glycosyl units can then be attached between their 1-position and the preceding glycosyl units 2-, 3-, 4- and/or 6-position, preferably predominately the 2-position.
  • condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol are also suitable for use as the additional nonionic surfactant of the nonionic surfactant systems of the present invention.
  • the hydrophobic portion of these compounds will preferably have a molecular weight of from about 1500 to about 1800 and will exhibit water insolubility.
  • the addition of polyoxyethylene moieties to this hydrophobic portion tends to increase the water solubility of the molecule as a whole, and the liquid character of the product is retained up to the point where the polyoxyethylene content is about 50% of the total weight of the condensation product, which corresponds to condensa ⁇ tion with up to about 40 moles of ethylene oxide.
  • Examples of compounds of this type include certain of the commercially- available PluronicTM surfactants, marketed by BASF. Also not preferred, although suitable for use as the addi ⁇ tional nonionic surfactant of the nonionic surfactant system of the present invention, are the condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylenediamine. The hydrophobic moiety of these products consists of the reaction product of ethylenediamine and excess propylene oxide, and generally has a molecular weight of from about 2500 to about 3000.
  • This hydrophobic moiety is con ⁇ densed with ethylene oxide to the extent that the condensation product contains from about 40% to about 80% by weight of polyoxy ⁇ ethylene and has a molecular weight of from about 5,000 to about 11,000.
  • nonionic surfactant include certain of the commercially available TetronicTM compounds, marketed by BASF.
  • Preferred for use as the additional nonionic surfactant of the nonionic surfactant systems of the present invention are polyethylene oxide condensates of alkyl phenols, condensation products of primary and secondary aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide, alkylpolysaccharides, and mixtures thereof.
  • C8-C14 alkyl phenol ethoxylates having from 3 to 15 ethoxy groups and Cs-Cis alcohol ethoxylates (preferably C10 avg.) having from 2 to 10 ethoxy groups, and mixtures thereof.
  • the present invention further provides laundry detergent compositions comprising at least 1% by weight, preferably from about 3% to about 65%, more preferably from about 10% to about 25% by weight of total surfactants.
  • the surfactants of such laundry detergent compositions can comprise only the nonionic surfactant system of the present invention, or it may comprise the nonionic surfactant system in combination with other detersive surfactants, such as anionic, cationic, ampholytic, zwitterionic and semi-polar surfactants.
  • the cationic surfactants useful herein are those having one long-chain hydrocarbly group.
  • the laundry detergent compositions of the present invention can also contain the optional nonionics already referred to herein, although it is believed that such optional nonionics do not provide the unexpected stain-removal benefits of the nonionic surfactant systems of the present invention.
  • the weight ratio of the nonionic surfactant system to the other detersive surfactants will be in the range of from about 50:1 to about 1:10, preferably from about 10:1 to about 1:5.
  • the laundry detergent compositions of the present invention can optionally contain other ingredients typically found in detergent compositions, such as builders, soil release agents, chelating agents, etc.
  • the nonionic surfactant systems of the present invention act to improve the greasy/oily stain removal properties of such laundry detergent compositions across a broad range of laundry conditions.
  • the laundry detergent compositions of the present invention can contain, in addition to the nonionic surfactant system of the present invention, one or more anionic surfactants as described below.
  • anionic surfactants as described below.
  • Alkyl ester sulfonate surfactants hereof include linear esters of C8-C20 carboxylic acids (i.e., fatty acids) which are sulfonated with gaseous SO3 according to "The Journal of the American Oil Chemists Society," 52 (1975), pp. 323-329. Suitable starting materials would include natural fatty substances as derived from tallow, palm oil, etc.
  • the preferred alkyl ester sulfonate surfactant especially for laundry applications, comprise alkyl ester sulfonate surfactants of the structural formula: 0
  • R3 - CH - C - 0R4 SO3M wherein R 3 is a C8-C20 hydrocarbyl, preferably an alkyl, or combination thereof, R 4 is a Ci-C ⁇ hydrocarbyl, preferably an alkyl, or combination thereof, and M is a cation which forms a water soluble salt with the alkyl ester sulfonate.
  • Suitable salt-forming cations include metals such as sodium, potassium, and lithium, and substituted or unsubstituted ammonium cations, such as monoethanolamine, diethanolamine, and triethanolamine.
  • R 3 is C10-C16 alkyl, and R* is methyl, ethyl or isopropyl.
  • the methyl ester sulfonates wherein R 3 is C10-C16 alkyl.
  • Alkyl sulfate surfactants hereof are water soluble salts or acids of the formula ROSO3M wherein R preferably is a C10-C24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C10-C20 alkyl component, more preferably a C12-C18 alkyl or hydroxyalkyl, and M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium), or ammonium or substituted ammonium (e.g., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations such as tetramethyl-ammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
  • R preferably is a C10-
  • alkyl chains of C12-I6 are preferred for lower wash temperatures (e.g., below about 50'C) and C16-I8 alkyl chains are preferred for higher wash temperatures (e.g., above about 50'C).
  • Alkyl alkoxylated sulfate surfactants hereof are water soluble salts or acids of the formula R0(A) m S03M wherein R is an unsubstituted C10-C24 alkyl or hydroxyalkyl group having a C10-C24 alkyl component, preferably a C12-C20 alkyl or hydroxyalkyl, more preferably C12-C18 alkyl or hydroxyalkyl, A is an ethoxy or propoxy unit, m is greater than zero, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3, and M is H or a cation which can be, for example, a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium, etc.), ammonium or substituted-ammonium cation.
  • R is an unsubstituted C10-C24 alkyl or hydroxyalkyl group having a C10-C24 alkyl component, preferably a C12-
  • Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
  • Specific examples of substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium cations and quaternary ammonium cations such as tetramethyl-ammonium and dimethyl piperdinium cations and those derived from alkyla ines such as ethylamine, diethylamine, triethylamine, mixtures thereof, and the like.
  • Exemplary surfactants are C1 -C18 alkyl polyethoxylate (1.0) sulfate (Ci2-Ci8E(1.0)M), C12-C18 alkyl polyethoxylate (2.25) sulfate (Ci2-Ci8E(2.25)M), C12-C18 alkyl polyethoxylate (3.0) sulfate (Ci2-Ci8E(3.0)M), and C12-C18 alkyl polyethoxylate (4.0) sulfate (Ci2-Ci8E(4.0)M), wherein M is conveniently selected from sodium and potassium.
  • anionic surfactants useful for detersive purposes can also be included in the laundry detergent compositions of the present invention. These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium).
  • salts such as mono-, di- and triethanolamine salts
  • soap C9-C20 l near alkylbenzenesulfonates, C8-C22 primary or secondary alkanesulfonates, C8-C24 olefinsulfonates, sulfonated polycarbox- ylic acids prepared by sulfonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British
  • acyl isethionates N-acyl taurates, alkyl succinamates and sulfo- succinates, monoesters of sulfosuccinates (especially saturated and unsaturated C12-C18 monoesters) and diesters of sulfosuccin- ates (especially saturated and unsaturated C6-C12 diesters), acyl sarcosinates, sulfates of alkylpolysaccharides such as the sul-
  • alkylpolyglucoside the nonionic nonsulfated compounds being described below
  • branched primary alkyl sulfates and alkyl polyethoxy carboxylates such as those of the formula RO(CH2CH2 ⁇ )k- CH2C00"M+ wherein R is a C8-C22 alkyl, k is an integer from 0 to 10, and M is a soluble salt-forming cation.
  • hydrogenated resin acids are also suitable, such as rosin, hydro ⁇ genated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil. Further examples are described in "Surface Active Agents and Detergents” (Vol. I and II by Schwartz, Perry and Berch). A variety of such surfactants are
  • laundry detergent compositions of the present invention typically comprise from about 1% to about 40%, preferably from about 3% to about 20% by weight of such anionic surfactants.
  • the laundry detergent compositions of the present invention may also contain cationic, ampholytic, zwitterionic, and semi- polar surfactants, as well as nonionic surfactants other than those already described herein.
  • cationic, ampholytic, zwitterionic, and semi- polar surfactants as well as nonionic surfactants other than those already described herein.
  • nonionic surfactants other than those already described herein, including the semi-polar nonionic amine oxides described below, will not provide the hereinbefore discussed stain removal benefits associated with the nonionic surfactant system of the present invention.
  • Cationic detersive surfactants suitable for use in the laundry detergent compositions of the present invention are those having one long-chain hydrocarbyl group.
  • cati ⁇ onic surfactants include the ammonium surfactants such as alkyldi ⁇ methylammonium halogenides, and those surfactants having the
  • R 2 is an alkyl or alkyl benzyl group having from about 8 to about 18 carbon atoms in the alkyl chain, each R 3 is selected from the group consisting of -CH2CH2-, -CH2CH(CH3)-,
  • each R* is selected from the group consisting of C1-C4 alkyl, C1-C4 hydroxy ⁇ alkyl, benzyl ring structures formed by joining the two R 4 groups, -CH2CH0H-CH0HC0R 6 CH0HCH20H wherein R ⁇ is any hexose or hexose polymer having a molecular weight less than about 1000, and
  • the laundry detergent compositions of the present invention typically comprise from 0% to about 25%, preferably from about 3% to about 15% by weight of such cationic surfactants.
  • Ampholytic surfactants are also suitable for use in the laundry detergent compositions of the present invention. These surfactants can be broadly described as aliphatic derivatives of secondary or tertiary amines, or aliphatic derivatives of heterocyclic secondary and tertiary amines in which the aliphatic
  • 10 radical can be straight- or branched-chain.
  • One of the aliphatic substituents contains at least about 8 carbon atoms, typically from about 8 to about 18 carbon atoms, and at least one contains an anionic water-solubilizing group, e.g., carboxy, sulfonate, sulfate. See U.S. Patent No. 3,929,678 to Laugh!in et al., issued 5 December 30, 1975 at column 19, lines 18-35 (herein incorporated by reference) for examples of ampholytic surfactants.
  • the laundry detergent compositions of the present invention typically comprise from 0% to about 15%, preferably from about 1% to about 10% by weight of such ampholytic 0 surfactants.
  • Zwitterionic surfactants are also suitable for use in laundry detergent compositions. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or
  • the laundry detergent compositions of the present invention typically comprise from 0% to about 15%, preferably from about 1% to about 10% by weight of such zwitterionic surfactants.
  • Semi-polar nonionic surfactants are a special category of
  • •sc nonionic surfactants which include water-soluble amine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxy ⁇ alkyl groups containing from about 1 to about 3 carbon atoms; and water-soluble sulfoxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to about 3 carbon atoms.
  • Semi-polar nonionic detergent surfactants include the amine oxide surfactants having the formula
  • R 5 O R (0R4) X (R5) 2 wherein R 3 is an alkyl, hydroxyalkyl, or alkyl phenyl group or mixtures thereof containing from about 8 to about 22 carbon atoms; R4 is an alkylene or hydroxyalkylene group containing from about 2 to about 3 carbon atoms or mixtures thereof; x is from 0 to about 3; and each R 5 is an alkyl or hydroxyalkyl group containing from about 1 to about 3 carbon atoms or a polyethylene oxide group containing from about 1 to about 3 ethylene oxide groups.
  • the R5 groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.
  • amine oxide surfactants in particular include Cio-Ci ⁇ alkyl dimethyl amine oxides and C8-C12 alkoxy ethyl dihydroxy ethyl amine oxides.
  • the laundry detergent compositions of the present invention typically comprise from 0% to about 15%, preferably from about 1% to about 10% by weight of such semi-polar nonionic surfactants.
  • Builders The laundry detergent compositions of the present invention can comprise inorganic or organic detergent builders to assist in mineral hardness control.
  • the level of builder can vary widely depending upon the end use of the composition and its desired physical form.
  • Liquid formulations typically comprise at least about 1%, more typically from about 5% to about 50%, preferably about 5% to about 30%, by weight of detergent builder.
  • Granular formulations typically comprise at least about 1%, more typically from about 10% to about 80%, preferably from about 15% to about 50% by weight of the detergent builder.
  • Lower or higher levels of builder, however, are not meant to be excluded.
  • Inorganic detergent builders include, but are not limited to,
  • alkali metal, ammonium and alkanolammonium salts of poly- phosphates (exemplified by the tripolyphosphates, pyrophosphates, and glassy polymeric eta-phosphates), phosphonates, phytic acid, silicates, carbonates (including bicarbonates and sesqui- carbonates), sulfates, and aluminosilicates.
  • poly- phosphates exemplified by the tripolyphosphates, pyrophosphates, and glassy polymeric eta-phosphates
  • phosphonates phosphonates
  • phytic acid silicates
  • carbonates including bicarbonates and sesqui- carbonates
  • sulfates sulfates
  • aluminosilicates aluminosilicates
  • borate builders builders containing borate-forming materials that can produce borate under detergent storage or wash conditions
  • non-borate builders are used in compositions of the invention intended for use at wash conditions less than about i5 50'C, especially less than about 40 * C.
  • silicate builders are the alkali metal silicates, particularly those having a Si ⁇ 2:Na2 ⁇ ratio in the range 1.6:1 to 3.2:1 and layered silicates, such as the layered sodium silicates described in U.S. Patent 4,664,839, issued May 12, 1987 to H. P.
  • silicates may also be useful such as for example magnesium silicate, which can serve as a crispening agent in granular formulations, as a stabilizing agent for oxygen bleaches, and as a component of suds control systems.
  • carbonate builders are the alkaline earth and alkali metal carbonates, including sodium carbonate and sesqui- carbonate and mixtures thereof with ultra-fine calcium carbonate as disclosed in German Patent Application No. 2,321,001 published on November 15, 1973, the disclosure of which is incorporated
  • Aluminosilicate builders are especially useful in the present invention. Aluminosilicate builders are of great importance in most currently marketed heavy duty granular detergent composi ⁇ tions, and can also be a significant builder ingredient in liquid
  • Aluminosilicate builders include those having the empirical formula:
  • Preferred aluminosilicates are zeolite builders which have the formula:
  • aluminosilicate ion exchange materials are commer ⁇ cially available. These aluminosilicates can be crystalline or amorphous in structure and can be naturally-occurring alumino ⁇ silicates or synthetically derived. A method for producing aluminosilicate ion exchange materials is disclosed in U.S.
  • Preferred synthetic crystalline alumino ⁇ silicate ion exchange materials useful herein are available under the designations Zeolite A, Zeolite P (B), and Zeolite X.
  • the crystalline aluminosilicate ion exchange material has the formula:
  • This material is known as Zeolite A.
  • the aluminosilicate has a particle size of about 0.1-10 microns in diameter.
  • Specific examples of polyphosphates are the alkali metal tripolyphosphates, sodium, potassium and ammonium pyrophosphate, sodium and potassium and ammonium pyrophosphate, sodium and potassium orthophosphate, sodium polymeta phosphate in which the degree of polymerization ranges from about 6 to about 21, and salts of phytic acid.
  • Examples of phosphonate builder salts are the water-soluble salts of ethane l-hydroxy-l,l-diphosphonate particularly the sodium and potassium salts, the water-soluble salts of methylene diphosphonic acid e.g. the trisodium and tripotassium salts and the water-soluble salts of substituted methylene diphosphonic acids, such as the trisodium and tripotassium ethylidene, isopyro ⁇ pylidene benzylmethylidene and halo methylidene phosphonates.
  • Phosphonate builder salts of the aforementioned types are dis ⁇ closed in U.S. Patent Nos.
  • Polycarboxylate builder can generally be added to the compo ⁇ sition in acid form, but can also be added in the form of a neutralized salt.
  • alkali metals such as sodium, potassium, and lithium salts, especially sodium salts, or ammonium and substituted ammonium (e.g., alkanolammonium) salts are preferred.
  • polycarboxylate builders include a variety of categories of useful materials.
  • One important category of poly- carboxylate builders encompasses the ether polycarboxylates.
  • a number of ether polycarboxylates have been disclosed for use as detergent builders.
  • Examples of useful ether polycarboxylates include oxydisuccinate, as disclosed in Berg, U.S. Patent 3,128,287, issued April 7, 1964, and Lamberti et al., U.S. Patent 3,635,830, issued January 18, 1972, both of which are incorporated herein by reference.
  • a specific type of ether polycarboxylates useful as builders in the present invention also include those having the general formula: CH(A)(C00X)-CH(C00X)-0-CH(C00X)-CH(C00X)(B) wherein A is H or OH; B is H or -0-CH(C00X)-CH2(C00X); and X is H or a salt-forming cation.
  • a and B are both H, then the compound is oxydissuccinic acid and its water-soluble salts. If A is OH and B is H, then the compound is tartrate monosuccinic acid (TMS) and its water-soluble salts.
  • TDS tartrate disuccinic acid
  • Suitable ether polycarboxylates also include cyclic com ⁇ pounds, particularly alicyclic compounds, such as those described in U.S.
  • Other useful detergency builders include the ether hydroxy- polycarboxylates represented by the structure:
  • n H0-[C(R)(C00M)-C(R)(C00M)-0] n -H wherein M is hydrogen or a cation wherein the resultant salt is water-soluble, preferably an alkali metal, ammonium or substituted ° ammonium cation, n is from about 2 to about 15 (preferably n is from about 2 to about 10, more preferably n averages from about 2 to about 4) and each R is the same or different and selected from hydrogen, C1-4 alkyl or C1-4 substituted alkyl (preferably R is hydrogen).
  • Still other ether polycarboxylates include copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1, 3, 5-trihydroxy benzene-2, 4, 6-trisulfonic acid, and carboxymethyl ⁇ oxysuccinic acid.
  • Organic polycarboxylate builders also include the various alkali metal, ammonium and substituted ammonium salts of poly- acetic acids.
  • polyacetic acid builder salts are the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediamine tetraacetic acid and nitrilotriacetic acid.
  • polycarboxylates such as mellitic acid, succinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, benezene pentacarboxylic acid, and carboxymethyloxysuccinic acid, and soluble salts thereof.
  • Citric builders e.g., citric acid and soluble salts thereof, is a polycarboxylate builder of particular importance for heavy duty liquid detergent formulations, but can also be used in granular compositions.
  • Suitable salts include the metal salts such as sodium, lithium, and potassium salts, as well as ammonium and substituted ammonium salts.
  • carboxylate builders include the carboxylated carbohy ⁇ drates disclosed in U.S. Patent 3,723,322, Diehl, issued March 28, 1973, incorporated herein by reference. Also suitable in the laundry detergent compositions of the present invention are the 3,3-dicarboxy-4-oxa-l,6-hexanedioates and the related compounds disclosed in U.S. Patent 4,566,984, Bush, issued January 28, 1986, incorporated herein by reference.
  • Useful succinic acid builders include the C5-C20 alkyl succinic acids and salts thereof. A particularly preferred compound of this type is dodecenylsuccinic acid.
  • Alkyl succinic acids typically are of the general formula R-CH(COOH)CH2(COOH) i.e., derivatives of succinic acid, wherein R is hydrocarbon, e.g., C10-C20 alkyl or alkenyl, preferably C12-C16 or wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, all as described in the above-mentioned patents.
  • R is hydrocarbon, e.g., C10-C20 alkyl or alkenyl, preferably C12-C16 or wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, all as described in the above-mentioned patents.
  • the succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanolammonium salts.
  • succinate builders include: lauryl- succinate, myristylsuccinate, palmitylsuccinate, 2-dodecenyl- succinate (preferred), 2-pentadecenylsuccinate, and the like. Laurylsuccinates are the preferred builders of this group, and are described in European Patent Application 86200690.5/0,200,263, published November 5, 1986.
  • useful builders also include sodium and potassium carboxymethyloxymalonate, carboxymethyloxysuccinate, cis-cyclo- hexanehexacarboxylate, cis-cyclopentane-tetracarboxylate, water- soluble polyacrylates (these polyacrylates having molecular weights to above about 2,000 can also be effectively utilized as dispersants), and the copolymers of maleic anhydride with vinyl methyl ether or ethylene.
  • polycarboxylates are the polyacetal carboxy- lates disclosed in U.S. Patent 4,144,226, Crutchfield et al., issued March 13, 1979, incorporated herein by reference. These polyacetal carboxylates can be prepared by bringing together, under polymerization conditions, an ester of glyoxylic acid and a polymerization initiator. The resulting polyacetal carboxylate ester is then attached to chemically stable end groups to stabil ⁇ ize the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted to the corresponding salt, and added to a surfactant.
  • Polycarboxylate builders are also disclosed in U.S. Patent 3,308,067, Diehl, issued March 7, 1967, incorporated herein by reference.
  • Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, esaconic acid, fumaric acid, aconitic acid, citraconic acid and methylene alonic acid.
  • Detersive enzymes can be included in the laundry detergent compositions of the present invention for a variety of reasons including removal of protein-based, carbohydrate-based, or triglyceride-based stains, for example, and prevention of refugee dye transfer.
  • the enzymes to be incorporated include proteases, amylases, lipases, cellulases, and peroxidases, as well as mixtures thereof. They may be of any suitable origin, such as vegetable, animal, bacterial, fungal and yeast origin. However, their choice is governed by several factors such as pH-activity and/or stability optima, thermostability, stability versus active detergents, builders and so on. In this respect bacterial or fungal enzymes are preferred, such as bacterial amylases and proteases, and fungal cellulases.
  • proteases are the subtilisins which are obtained from particular strains of B.subtilis and B.licheniforms. Another suitable protease is obtained from a strain of Bacillus, having maximum activity throughout the pH range of 8-12, developed and sold by Novo Industries A/S under the registered trade name Esperase®. The preparation of this enzyme and analogous enzymes is described in British patent specification No. 1,243,784 of Novo.
  • proteolytic enzymes suitable for removing protein-based stains that are commercially available include those sold under the tradenames ALCALASETM and SAVINASETM by Novo Industries A/S (Denmark) and MAXATASETM by International Bio-Synthetics, Inc. (The Netherlands). Of interest in the category of proteolytic enzymes, espe ⁇ cially for liquid detergent compositions, are enzymes referred to herein as Protease A and Protease B. Protease A and methods for its preparation are described in European Patent Application
  • Protease B is a proteolytic enzyme which differs from Protease A in that it has a leucine substituted for tyrosine in position 217 in its amino acid sequence. Protease B is described in European Patent Application Serial No. 87303761.8, filed April
  • Amylases include, for example, ⁇ -amylases obtained from a
  • Amylolytic proteins include, for example, RAPIDASETM, International Bio-Synthetics, Inc. and TERMAMYLTM, NOVO Industries.
  • the cellulases usable in the present invention include both bacterial or fungal cellulase. Preferably, they will have a pH optimum of between 5 and 9.5. Suitable cellulases are disclosed in U.S. Patent 4,435,307, Barbesgoard et al., issued March 6, 1984, incorporated herein by reference, which discloses fungal
  • cellulase produced from Humicola insolens Suitable cellulases are also disclosed in GB-A-2.075.028; GB-A-2.095.275 and DE-OS-2.247.832.
  • cellulases produced by a strain of Humicola insolens (Humicola grisea var. thermoidea),
  • Humicola strain DSM 1800 and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging to the genus Aeromonas, and cellulase extracted from the hepatopancreas of a marine mollusc (Dolabella Auricula Solander).
  • Suitable lipase enzymes for detergent usage include those
  • Suitable lipases include those which show a positive immunological cross-reaction with the antibody of the lipase, produced by the microorganism Pseudomonas fluorescens IAM 1057. This lipase and a method for its purification have been described in Japanese Patent Application No. 53-20487, laid open to public inspection on 5 February 24, 1978. This lipase is available from Amano Pharmaceutical Co.
  • Lipase P Lipase P
  • Amano-P Lipase P
  • Such lipases of the present invention should show a positive immuno ⁇ logical cross reaction with the Amano-P antibody, using the 10 standard and well-known im unodiffusion procedure according to Ouchterlony (Acta. Med. Scan., 133, pages 76-79 (1950)).
  • These lipases, and a method for their immunological cross-reaction with Amano-P are also described in U.S. Patent 4,707,291, Thorn et al., issued November 17, 1987, incorporated herein by reference. -- Typical examples thereof are the Amano-P lipase, the lipase ex
  • Peroxidase enzymes are used in combination with oxygen 5 sources, e.g., percarbonate, perborate, persulfate, hydrogen peroxide, etc. They are used for "solution bleaching,” i.e. to prevent transfer of dyes or pigments removed from substrates during wash operations to other substrates in the wash solution.
  • Peroxidase enzymes are known in the art, and include, for example, 0 horseradish peroxidase, ligninase, and haloperoxidase such as chloro- and bromo-peroxidase.
  • Peroxidase-containing detergent compositions are disclosed, for example, in PCT International
  • Enzymes are further disclosed in U.S. Patent No. 4,101,457, Place et al., issued July 18, 1978, and in U.S. Patent 4,507,219, Hughes, issued March 26, 1985, both incorporated herein by reference. Enzyme materials useful for liquid detergent formulations, and their incorporation into such formulations, are disclosed in U.S. Patent 4,261,868, Hora et al., issued April 14, 1981, also incorporated herein by reference.
  • Enzymes are normally incorporated at levels sufficient to provide up to about 5 mg by weight, more typically about 0.05 mg to about 3 mg, of active enzyme per gram of the composition.
  • the enzymes are preferably coated or prilled with additives inert toward the enzymes to minimize dust formation and improve storage stability. Techniques for accom ⁇ plishing this are well known in the art.
  • an enzyme stabilization system is preferably utilized. Enzyme stabilization techniques for aqueous detergent compositions are well known in the art. For example, one technique for enzyme stabilization in aqueous solutions involves the use of free calcium ions from sources such as calcium acetate, calcium for ⁇ mate, and calcium propionate.
  • Calcium ions can be used in combi- nation with short chain carboxylic acid salts, preferably for ⁇ mates. See, for example, U.S. Patent 4,318,818, Letton, et al., issued March 9, 1982, incorporated herein by reference. It has also been proposed to use polyols like glycerol and sorbitol. Alkoxy-alcohols, dialkylglycoethers, mixtures of polyvalent alcohols with polyfunctional aliphatic amines (e.g., alkanolamines such as diethanolamine, triethanolamine, di-isopropanolamine, etc.), and boric acid or alkali metal borate.
  • polyols like glycerol and sorbitol.
  • Alkoxy-alcohols dialkylglycoethers
  • mixtures of polyvalent alcohols with polyfunctional aliphatic amines e.g., alkanolamines such as diethanolamine, triethanolamine, di-isopropan
  • Enzyme stabiliza ⁇ tion techniques are additionally disclosed and exemplified in U.S. Patent 4,261,868, issued April 14, 1981 to Horn, et al., U. S. Patent 3,600,319, issued August 17, 1971 to Gedge, et al., both incorporated herein by reference, and European Patent Application Publication No. 0 199 405, Application No. 86200586.5, published October 29, 1986, Venegas.
  • Non-boric acid and borate stabilizers are preferred.
  • Enzyme stabilization systems are also described, for example, in U.S. Patents 4,261,868, 3,600,319, and 3,519,570.
  • the laundry detergent compositions of the present invention may contain bleaching agents or bleaching compositions containing bleaching agent and one or more bleach activators.
  • present bleaching compounds will typically comprise from about 1% to about 20%, more typically from about 1% to about 10%, of such laundry detergent composition.
  • bleaching compounds are optional components in non-liquid formulations, e.g., granular detergents. If present, the amount of bleach activators will typically be from about 0.1% to about 60%, more typically from about 0.5% to about 40% of the bleaching composition.
  • the bleaching agents used herein can be any of the bleaching agents useful for detergent compositions in textile cleaning, hard surface cleaning, or other cleaning purposes that are now known or become known. These include oxygen bleaches as well as other bleaching agents.
  • the compositions hereof not contain borate or material which can form borate in situ (i.e. borate-forming material) under detergent storage or wash conditions.
  • borate-forming material i.e. borate-forming material
  • detergents to be used at these temperatures are substan- tially free of borate and borate-forming material.
  • substantially free of borate and borate-forming material shall mean that the composition contains not more than about 2% by weight of borate-containing and borate-forming material of any type, preferably, no more than 1%, more preferably 0%.
  • One category of bleaching agent that can be used encompasses percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxy- phthalate hexahydrate, the magnesium salt of meta-chloro perbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydodecanedioic acid.
  • Such bleaching agents are disclosed in U.S. Patent 4,483,781, Hartman, issued November 20, 1984, U.S.
  • Highly preferred bleaching agents also include 6-nonyl- amino-6-oxoperoxycaproic acid as described in U.S. Patent 4,634,551, issued January 6, 1987 to Burns, et al., incorporated herein by reference.
  • bleaching agents that can be used encompasses the halogen bleaching agents.
  • hypohalite bleaching agents include trichloro isocyanuric acid and the sodium and potassium diehloroisocyanurates and N-chloro and N-bromo alkane sulfonamides. Such materials are normally added at 0.5-10% by weight of the finished product, preferably 1-5% by weight.
  • Peroxygen bleaching agents can also be used. Suitable peroxygen bleaching compounds include sodium carbonate peroxy ⁇ hydrate, sodium pyrophosphate peroxyhydrate, urea peroxyhydrate, and sodium peroxide.
  • Peroxygen bleaching agents are preferably combined with bleach activators, which lead to the in situ production in aqueous solution (i.e., during the washing process) of the peroxy acid corresponding to the bleach activator.
  • Preferred bleach activators incorporated into the laundry detergent compositions of the present invention have the general formula:
  • R is an alkyl group containing from about 1 to about 18 carbon atoms wherein the longest linear alkyl chain extending from and including the carbonyl carbon contains from about 6 to about
  • Bleaching agents other than oxygen bleaching agents are also known in the art and can be utilized herein.
  • One type of non- oxygen bleaching agent of particular interest includes photo- activated bleaching agents such as the sulfonated zinc and/or aluminum phthalocyanines. These materials can be deposited upon the substrate during the washing process. Upon irradiation with light, in the presence of oxygen, such as by hanging clothes out to dry in the daylight, the sulfonated zinc phthalocyanine i activated and, consequently, the substrate is bleached.
  • Preferre zinc phthalocyanine and a photoactivated bleaching process ar described in U.S. Patent 4,033,718, issued July 5, 1977 t Holcombe et al., incorporated herein by reference.
  • detergent compositions will contain about 0.025% to about 1.25%, by weight, of sulfonated zinc phthalocyanine.
  • polymeric soil release agents Any polymeric soil release agents known to those skilled i the art can be employed in the laundry detergent compositions o the present invention.
  • Polymeric soil release agents are characterized by having both 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 and, thus, serve as an anchor for the hydrophilic segments. This can enable stains occurring subsequent to treatment with the soil release agent to be more easily cleaned in later washing procedures.
  • Polymeric soil release agents include cellulosic derivatives such as hydroxyether cellulosic polymers, copolymeric blocks of ethylene terephthalate or propylene terephthalate with polyethylene oxide or polypropylene oxide terephthalate, and the like.
  • Cellulosic derivatives that are functional as soil release agents are commercially available and include hydroxyethers of cellulose such as MethocelR (Dow).
  • Cellulosic soil release agents also include those selected from the group consisting of C1-C4 alkyl and C4 hydroxyalkyl cellulose such as methylcellulose, ethylcellulose, hydroxypropyl methylcellulose, and hydroxybutyl methylcellulose.
  • C1-C4 alkyl and C4 hydroxyalkyl cellulose such as methylcellulose, ethylcellulose, hydroxypropyl methylcellulose, and hydroxybutyl methylcellulose.
  • a variety of cellulose derivatives useful as soil release polymers are disclosed in U.S. Patent 4,000,093, issued December 28, 1976 to Nicol, et al., incorporated herein by reference.
  • Soil release agents characterized by poly(vinyl ester) hydrophobe segments include graft copolymers of poly(vinyl ester), e.g., Ci-C ⁇ vinyl esters, preferably poly(vinyl acetate) grafted onto polyalkylene oxide backbones, such as polyethylene oxide backbones.
  • poly(vinyl ester) e.g., Ci-C ⁇ vinyl esters
  • poly(vinyl acetate) grafted onto polyalkylene oxide backbones such as polyethylene oxide backbones.
  • Such materials are known in the art and are described in European Patent Application 0219048, published April 22, 1987 by Kud, et al .
  • Suitable commercially available soil release agents of this kind include the SokalanTM type of material, e.g., SokalanTM HP-22, available from BASF (West Germany).
  • One type of preferred soil release agent is a copolymer having random blocks of ethylene terephthalate and polyethylene oxide (PEO) terephthalate. More specifically, these polymers are comprised of repeating units of ethylene terephthalate and PEO terephthalate in a mole ratio of ethylene terephthalate units to PEO terephthalate units of from about 25:75 to about 35:65, said PEO terephthalate units containing polyethylene oxide having molecular weights of from about 300 to about 2000. The molecular weight of this polymeric soil release agent is in the range of from about 25,000 to about 55,000. See U.S. Patent 3,959,230 to
  • Another preferred polymeric soil release agent is a polyester with repeat units of ethylene terephthalate units containing 10-15% by weight of ethylene terephthalate units together with 90-80% by weight of polyoxyethylene terephthalate units, derived from a polyoxyethylene glycol of average molecular weight 300-5,000, and the mole ratio of ethylene terephthalate units to polyoxyethylene terephthalate units in the polymeric compound is between 2:1 and 6:1.
  • this polymer include the commercially available material Zelcon R 5126 (from Dupont) and Milease R T (from ICI). These polymers and methods of their preparation are more fully described in U.S. Patent 4,702,857, issued October 27, 1987 to Gosselink, which is incorporated herein by reference.
  • Another preferred polymeric soil release agent is a sulfonated product of a substantially linear ester oligomer comprised of an oligomeric ester backbone of terephthaloyl and oxyalkyleneoxy repeat units and terminal moieties covalently attached to the backbone, said soil release agent being derived from allyl alcohol ethoxylate, dimethylterephthalate, and 1,2 propylene diol, wherein the terminal moieties of each oligomer have, on average, a total of from about 1 to about 4 sulfonate groups.
  • These soil release agents are described fully in U.S. Patent 4,968,451, issued November 6, 1990 to J. J. Scheibel and E. P. Gosselink, U.S. Serial No. 07/474,709, filed January 29, 1990, 5 incorporated herein by reference.
  • Suitable polymeric soil release agents include the ethyl- or methyl-capped 1,2-propylene terephthalate-polyoxy- ethylene terephthalate polyesters of U.S. Patent 4,711,730, issued December 8, 1987 to Gosselink et al., the anionic end-capped 10 oligomeric esters of U.S. Patent 4,721,580, issued January 26, 1988 to Gosselink, wherein the anionic end-caps comprise sulfo-polyethoxy groups derived from polyethylene glycol (PEG), the block polyester oligomeric compounds of U.S.
  • PEG polyethylene glycol
  • Patent 4,702,857 issued October 27, 1987 to Gosselink, having polyethoxy end-caps 15 of the formula X-(0CH2CH2)rr wherein n is from 12 to about 43 and X is a C1-C4 alkyl, or preferably methyl, all of these patents being incorporated herein by reference.
  • Additional soil release polymers include the soil release polymers of U.S. Patent 4,877,896, issued October 31, 1989 to Q Maldonado et al., which discloses anionic, especially sulfoaroyl, end-capped terephthalate esters, said patent being incorporated herein by reference.
  • the terephthalate esters contain unsymmet- rically substituted oxy-1,2-alkyleneoxy units.
  • soil release agents will generally comprise from 5 about 0.01% to about 10.0%, preferably from about 0.1% to about 5.0%, more preferably from about 0.2% to about 3.0% by weight of the laundry detergent compositions of the present invention.
  • the laundry detergent compositions of the present invention 0 may also optionally contain one or more iron and manganese chelat ⁇ ing agents as a builder adjunct material.
  • Such chelating agents can be selected from the group consisting of amino carboxylates, amino phosphonates, polyfunctionally-substituted aromatic chelat ⁇ ing agents and mixtures thereof, all as hereinafter defined. ⁇ Without intending to be bound by theory, it is believed that the benefit of these materials is due in part to their exceptional ability to remove iron and manganese ions from washing solutions by formation of soluble chelates.
  • Amino carboxylates useful as optional chelating agents in compositions of the invention can have one or more, preferably at least two, units of the substructure
  • M is hydrogen, alkali metal, ammonium or substituted ammonium (e.g. ethanolamine) and x is from 1 to about 3, pref- 0 erably 1.
  • these amino carboxylates do not contain alkyl or alkenyl groups with more than about 6 carbon atoms.
  • Operable amine carboxylates include ethylenediaminetetraacetates, N-hydroxyethylethylenediaminetriacetates, nitri1otriacetates, ethylenediamine tetraproprionates, triethylenetetraaminehexa- 5 acetates, diethylenetriaminepentaacetates, and ethanoldiglycines, alkali metal, ammonium, and substituted ammonium salts thereof and mixtures thereof.
  • Amino phosphonates are also suitable for use as chelating agents in the laundry detergent compositions of the present f) invention when at least low levels of total phosphorus are permitted in detergent compositions.
  • Compounds with one or more, preferably at least two, units of the substructure are also suitable for use as chelating agents in the laundry detergent compositions of the present f) invention when at least low levels of total phosphorus are permitted in detergent compositions.
  • M is hydrogen, alkali metal, ammonium or substituted ammonium and x is from 1 to about 3, preferably 1, are useful and include ethylenediaminetetrakis (methylenephosphonates), nitrilo- 0 tris (methylenephosphonates) and diethylenetriaminepentakis (methylenephosphonates).
  • these amino phosphonates do not contain alkyl or alkenyl groups with more than about 6 carbon atoms.
  • Alkylene groups can be shared by substructures.
  • Polyfunctionally-substituted aromatic chelating agents are 5 also useful in the compositions herein. These materials can comprise compounds having the general formula R wherein at least one R is -SO3H or -COOH or soluble salts thereof and mixtures thereof.
  • Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as l,2-dihydroxy-3,5-disulfobenzene.
  • Alkaline detergent compositions can contain these materials in the form of alkali metal, ammonium or substituted ammonium (e.g.
  • these chelating agents will generally comprise from about 0.1% to about 10% by weight of the laundry detergent compositions of the present invention. More preferably chelating agents will comprise from about 0.1% to about 3.0% by weight of such compositions.
  • Clay Soil Removal/Anti-redeposition Agents will generally comprise from about 0.1% to about 10% by weight of the laundry detergent compositions of the present invention. More preferably chelating agents will comprise from about 0.1% to about 3.0% by weight of such compositions.
  • Clay soil removal/anti-redeposition agents useful in the laundry detergent compositions of the present invention include polyethylene glycols and water-soluble ethoxylated amines having clay soil removal and anti-redeposition properties.
  • Polyethylene glycol compounds useful in the laundry detergent compositions of the present invention typically have a molecular weight in the range of from about 400 to about 100,000, preferably from about 1,000 to about 20,000, more preferably from about 2,000 to about 12,000, most preferably from about 4,000 to about 8,000.
  • Such compounds are commercially available and are sold as Carbowax®, which is available from Union Carbide, located in Danbury, Conn.
  • the water-soluble ethoxylated amines are preferably selected from the group consisting of: (l) ethoxylated monoamines having the formula:
  • R is H or C1-C4 alkyl or hydroxyalkyl
  • Rl is C2-C12 alkylene, hydroxyalkyl ene, alkenyl ene, aryl ene or alkarylene, or a
  • each R 2 is C1-C4 or hydroxyalkyl, the moiety -L-X, or two R 2 together form the moiety -(CH2)r> -A 2 -(CH2)s-.
  • a 2 is -0- or -CH2-, r is 1 or 2, s is 1 or 2, and r + s is 3 or 4;
  • X is a nonionic group, an anionic group or mixture thereof;
  • R 3 is a substituted C3-C12 alkyl, hydroxyalkyl, alkenyl, aryl, or alkaryl group having substitution sites;
  • R 4 is C1-C12 alkylene, hydroxyalkyl ene, alkenylene, arylene or alkarylene, or a C2-C3 oxyalkylene moiety having from 2 to about 20 oxyalkylene units provided that no 0-0 or 0-N bonds are formed;
  • L is a hydrophilic chain which contains the polyoxyalkyl ⁇ ene moiety -[(R 5 0) m (CH2CH2 ⁇ ) n ]-, wherein R5 is C3-C4 alkylene or hydroxyalkyl ene and m and n are numbers such that the
  • the most preferred soil release and anti-redeposition agent is ethoxylated tetraethylenepentamine.
  • Exemplary ethoxylated amines are further described in U.S. Patent 4,597,898, VanderMeer, issued July 1, 1986, incorporated herein by reference.
  • Another group of preferred clay soil removal/anti- redeposition agents are the cationic compounds disclosed in European Patent Application 111,965, Oh and Gosselink, published June 27, 1984, incorporated herein by reference.
  • clay soil removal/anti-redeposition agents which can be used include the ethoxylated amine polymers disclosed in European Patent Applica- tion 111,984, Gosselink, published June 27, 1984; the zwitterionic polymers disclosed in European Patent Application 112,592, Gosselink, published July 4, 1984; and the amine oxides disclosed in U.S. Patent 4,548,744, Connor, issued October 22, 1985, all of which are incorporated herein by reference.
  • the most preferred soil release and anti-redeposition agents are ethoxylated tetraethylenepentamine and the polyethylene glycols having a molecular weight in the range of from about 4,000 to about 8,000.
  • Granular detergent compositions which contain such compounds typically contain from about 0.01% to about 10.0% by weight of the clay removal agent; liquid detergent compositions typically contain from about 0.01% to about 5.0% by weight.
  • Polymeric Dispersing Agents typically contain from about 0.01% to about 10.0% by weight of the clay removal agent; liquid detergent compositions typically contain from about 0.01% to about 5.0% by weight.
  • Polymeric polycarboxylate dispersing agents can advanta- geously be utilized in the laundry detergent compositions of the present invention. These materials can aid in calcium and magne ⁇ sium hardness control. In addition to acting as a builder adjunct analogously to the polycarboxylate described above in the Builder description, it is believed, though it is not intended to be limited by theory, that these higher molecular weight dispersing agents can further enhance overall detergent builder performance by inhibiting crystal growth of inorganics, by particulate soil peptization, and by antiredepositions, when used in combination with other builders including lower molecular weight polycarboxylates.
  • polycarboxylate materials which can be employed as the polymeric polycarboxylate dispersing agent are these polymers or copolymers which contain at least about 60% by weight of segments with the general formula
  • X, Y, and Z are each selected from the group consisting of hydrogen, methyl, carboxy, carboxymethyl, hydroxy and hydroxy- methyl ; a salt-forming cation and n is from about 30 to about 400.
  • X is hydrogen or hydroxy
  • Y is hydrogen or carboxy
  • Z is hydrogen
  • M is hydrogen, alkali metal, ammonia or substituted ammonium.
  • Polymeric polycarboxylate materials of this type can be prepared by polymerizing or copolymerizing suitable unsaturated monomers, preferably in their acid form.
  • Unsaturated monomeric acids that can be polymerized to form suitable polymeric poly ⁇ carboxylates include acrylic acid, maleic acid (or maleic anhydride), fumaric acid, itaconic acid, aconitic acid, mesaconic acid, citraconic acid and methylenema!onic acid.
  • the presence in the polymeric polycarboxylates herein of monomeric segments, containing no carboxylate radicals such as vinyl ethyl ether, styrene, ethylene, etc. is suitable provided that such segments do not constitute more than about 40% by weight.
  • Particularly suitable polymeric polycarboxylates can be derived from acrylic acid.
  • acrylic acid-based polymers which are useful herein are the water-soluble salts of polymerized acrylic acid.
  • the average molecular weight of such polymers in the acid form ranges from about 2,000 to 10,000, more preferably from about 4,000 to 7,000 and most preferably from about 4,000 to 5,000.
  • Water-soluble salts of such acrylic acid polymers can include, for example, the alkali metal, ammonium and substituted ammonium salts. Soluble polymers of this type are known materials. Use of polyacrylates of this type in detergent compositions has been disclosed, for example, in Diehl, U.S. Patent No. 3,308,067, issued March 7, 1967. This patent is incorporated herein by reference.
  • Acrylic/maleic-based copolymers may also be used as a preferred component of the dispersing agent.
  • Such materials include the water-soluble salts of copolymers of acrylic acid and maleic acid.
  • the average molecular weight of such copolymers in the acid form ranges from about 5,000 to 100,000, preferably from about 6,000 to 60,000, more preferably from about 7,000 to 60,000.
  • the ratio of acrylate to maleate segments in such copolymers will generally range from about 30:1 to about 1:1, more preferably from about 10:1 to 2:1.
  • Water-soluble salts of such acrylic acid/ maleic acid copolymers can include, for example, the alkali metal, ammonium and substituted ammonium salts. Soluble acryl te/ aleate copolymers of this type are known materials which are described in European Patent Application No. 66915, published December 15, 1982, which publication is incorporated herein by reference.
  • the polymeric dispersing agents will generally comprise from about 0.2% to about 10%, preferably from about 1% to about 5% by weight of the laundry detergent compositions.
  • Brightener preferably from about 1% to about 5% by weight of the laundry detergent compositions.
  • Optical brighteners or other brightening or whitening agents known to those skilled in the art can be incorporated into the laundry detergent compositions of the present invention.
  • the choice of brightener will depend upon a number of factors, such as the type of detergent, the nature of other components present in the detergent composition, the temperatures of wash water, the degree of agitation, and the ratio of the material washed to tub size.
  • the brightener selection is also dependent upon the type of material to be cleaned, e.g., cottons, synthetics, etc. Since most laundry detergent products are used to clean a variety of fabrics, the detergent compositions should contain a mixture of brighteners which will be effective for a variety of fabrics. It is of course necessary that the individual components of such a brightener mixture be compatible.
  • Commercial optical brighteners can be classified into subgroups which include, but are not necessarily limited to, derivatives of stilbene, pyrazoline, coumarin, carboxylic acid, methinecyanines, dibenzothiphene-5,5-dioxide, azoles, 5- and 6-membered-ring heterocycles, and other miscellaneous agents. Examples of such brighteners are disclosed in "The Production and Application of Fluorescent Brightening Agents", M. Zahradnik, Published by John Wiley & Sons, New York (1982), the disclosure of which is incorporated herein by reference.
  • Stilbene derivatives include, but are not necessarily limited to, derivatives of bis(triazinyl)amino-stilbene; bisacylamino derivatives of stilbene; triazole derivatives of stilbene; oxadia- zole derivatives of stilbene; oxazole derivatives of stilbene; and styryl derivatives of stilbene.
  • bis(triazinyl)aminostilbene may be prepared from 4,4'-diamine-stilbene-2,2'-disulfonic acid.
  • Coumarin derivatives include, but are not necessarily limited to, derivatives substituted in the 3-position, in the 7-position, and in the 3- and 7-positions.
  • Carboxylic acid derivatives include, but are not necessarily limited to, fumaric acid derivatives; benzoic acid derivatives; p-phenylene-bis-acrylic acid derivatives; naphthalenedicarboxylic acid derivatives; heterocyclic acid derivatives; and cinnamic acid derivatives.
  • Cinnamic acid derivatives can be further subclassified into groups which include, but are not necessarily limited to, cinnamic acid derivatives, styrylazoles, styrylbenzofurans, styryloxadia- zoles, styryltriazoles, and styrylpolyphenyls, as disclosed on page 77 of the Zahradnik reference.
  • the styrylazoles can be further subclassified into styryl- benzoxazoles, styrylimidazoles and styrylthiazoles, as disclosed on page 78 of the Zahradnik reference. It will be understood that these three identified subclasses may not necessarily reflect an exhaustive list of subgroups into which styrylazoles may be subclassified.
  • optical brighteners are the derivatives of dibenzothio- phene-5,5-dioxide disclosed at page 741-749 of The Kirk-Othmer Encyclopedia of Chemical Technology. Volume 3, pages 737-750 (John Wiley & Son, Inc., 1962), the disclosure of which is incorporated herein by reference, and include 3,7-diaminodibenzothiophene-2,8- disulfonic acid 5,5 dioxide.
  • optical brighteners are azoles, which are derivatives of 5-membered ring heterocycles. These can be further subcategor- ized into monoazoles and bisazoles. Examples of monoazoles and bisazoles are disclosed in the Kirk-Othmer reference.
  • Still other optical brighteners are the derivatives of 6-membered-ring heterocycles disclosed in the Kirk-Othmer refer- ence. Examples of such compounds include brighteners derived from pyrazine and brighteners derived from 4-aminonaphthalamide.
  • miscellane ⁇ ous agents may also be useful as brighteners.
  • miscellaneous agents are disclosed at pages 93-95 of the Zahradnik reference, and include l-hydroxy-3,6,8-pyrenetri- sulfonic acid; 2,4-dimethoxy-1,3,5-triazin-6-yl-pyrene; 4,5-di- phenylimidazol- onedisulfonic acid; and derivatives of pyrazoline- quinoline.
  • optical brighteners are those identified in U.S. Patent 4,790,856, issued to Wixon on December 13, 1988, the disclosure of which is incorporated herein by reference. These brighteners include the PhorwhiteTM series of brighteners from Verona.
  • Tinopal UNPA Tinopal CBS and Tinopal 5BM
  • Ciba-Geigy available from Ciba-Geigy
  • Arctic White CC available from Hilton-Davis, located in Italy
  • 2-(4-styryl- phenyl)-2H-naphthol[l,2-d]triazoles 4,4'-bis-(l,2,3-triazol-2- yl)-stilbenes
  • 4,4'-bis(styryl)bisphenyls 4,4'-amino- coumarins.
  • these brighteners include 4-methyl-7-diethylamino coumarin; l,2-bis(-benzimidazol-2-yl)- ethylene; 1,3-diphenylphrazolines; 2,5-bis(benzoxazol-2-yl)- thiophene; 2-styryl-naphth-[l,2-d]-oxazole; and 2-(stilbene-4-yl)- 2H-naphtho[l,2-d]triazole.
  • Still other optical brighteners include those disclosed in U.S. Patent 3,646,015, issued February 29, 1972 to Hamilton, the disclosure of which is incorporated herein by reference.
  • optical brighteners will generally comprise
  • laundry detergent compositions of the present invention 10 laundry detergent compositions of the present invention.
  • Suds suppressors can be desirable because the polyhydroxy fatty acid amide surfactants hereof can increase suds stability of the detergent compositions. Suds suppression can be of particular importance
  • detergent compositions include a relatively high sudsing surfactant in combination with the polyhydroxy fatty acid amide surfactant. Suds suppression is particularly desirable for compositions intended for use in front loading automatic washing machines. These machines are typically characterized by having
  • Suds suppressors are well known to those skilled in the art. They are generally described, for example, in Kirk Oth er Encyclopedia of Chemical Technology, Third Edition, Volume 7, pages 430-447
  • One category of suds suppressor of particular interest encompasses monocarboxylic fatty acids and soluble salts thereof. These materials are discussed in U.S. Patent 2,954,347, issued September 27, 1960 to Wayne St. John, said patent being incorporated herein by reference.
  • the monocar- c boxylic fatty acids, and salts thereof, for use as suds suppressor typically have hydrocarbyl chains of 10 to about 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. These materials are a preferred category of suds suppressor for detergent compositions.
  • the laundry detergent compositions of the present invention may also contain non-surfactant suds suppressors.
  • non-surfactant suds suppressors include, for example, high molecular weight hydrocarbons such as paraffin, fatty acid esters (e.g., fatty acid triglycerides), fatty acid esters of monovalent alcohols, aliphatic C18-C40 ketones (e.g. stearone), etc.
  • suds inhibitors include N-alkylated amino triazines such as tri- to hexa-alkylmelamines or di- to tetra- alkyldiamine chlortriazines formed as products of cyanuric chlor ⁇ ide with two or three moles of a primary or secondary amine containing 1 to 24 carbon atoms, propylene oxide, and monostearyl phosphates such as monostearyl alcohol phosphate ester and mono ⁇ stearyl di-alkali metal (e.g., sodium, potassium, lithium) phos- phates and phosphate esters.
  • the hydrocarbons, such as paraffin and haloparaffin can be utilized in liquid form.
  • the liquid hydrocarbons will be liquid at room temperature and atmospheric pressure, and will have a pour point in the range of about -40*C and about 5 * C, and a minimum boiling point not less than about 110'C (atmospheric pressure). It is also known to utilize waxy hydrocarbons, preferably having a melting point below about lOO'C.
  • the hydrocarbons constitute a preferred category of suds suppres ⁇ sor for detergent compositions. Hydrocarbon suds suppressors are described, for example, in U.S. Patent 4,265,779, issued May 5, 1981 to Gandolfo, et al., incorporated herein by reference.
  • the hydrocarbons thus, include aliphatic, alicyclic, aromatic, and heterocyclic saturated or unsaturated hydrocarbons having from about 12 to about 70 carbon atoms.
  • the term "paraffin,” as used in this suds suppressor discussion, is intended to include mix- tures of true paraffins and cyclic hydrocarbons.
  • Non-surfactant suds comprises silicone suds suppressors.
  • This category includes the use of polyorganosiloxane oils, such as polydimethylsiloxane, dispersions or emulsions of polyorganosiloxane oils or resins, and combinations of polyorganosiloxane with silica particles wherein the polyorganosiloxane is chemisorbed of fused onto the silica.
  • Silicone suds suppressors are well known in the art and are, for example, disclosed in U.S. Patent 4,265,779, issued May 5, 1981 to Gandolfo et al . and European Patent Application No. 89307851.9, published February 7, 1990, by Starch, M. S., both incorporated herein by reference.
  • silicone and silanated silica are described, for instance, in German Patent Application DOS 2,124,526.
  • Silicone defoamers and suds controlling agents in granular detergent compositions are disclosed in U.S. Patent 3,933,672, Bartolotta et al., and in U.S. Patent 4,652,392, Baginski et al., issued March 24, 1987.
  • An exemplary silicone based suds suppressor for use herein is a suds suppressing amount of a suds controlling agent consisting essentially of:
  • the laundry detergent compositions of the present invention will generally comprise from 0% to about 5% of suds suppressor.
  • suds suppressors When utilized as suds suppressors, monocarboxylic fatty acids, and salts thereof, will be present typically in amounts up to about 5%, by weight, of the detergent composition.
  • Silicone suds suppressors are typically utilized in amounts up to about 2.0%, by weight, of the detergent composition, although higher amounts may be used. This upper limit is practical in nature, due primarily to concern with keeping costs 5 minimized and effectiveness of lower amounts for effectively controlling sudsing.
  • silicone suds suppressor Preferably from about 0.01% to about 1% of silicone suds suppressor is used, more preferably from about 0.25% to about 0.5%.
  • these weight percentage values include any silica that may be utilized in combination with 10 polyorganosiloxane, as well as any adjunct materials that may be utilized.
  • Monostearyl phosphates are generally utilized in amounts ranging from about 0.1% to about 2% by weight of the compositions.
  • Hydrocarbon suds suppressors are typically utilized in -- amounts ranging from about 0.01% to about 5.0%, although higher levels can be used.
  • Other Ingredients are typically utilized in -- amounts ranging from about 0.01% to about 5.0%, although higher levels can be used.
  • a wide variety of other ingredients which can be included in the laundry detergent compositions of the present invention 2 ⁇ include other active ingredients, carriers, hydrotropes, process ⁇ ing aids, dyes or pigments, solvents for liquid formulations, etc.
  • Liquid detergent compositions can contain water and other solvents as carriers. Low molecular weight primary or secondary alcohols exemplified by methanol, ethanol, propanol, and iso- propanol are suitable.
  • Monohydric alcohols are preferred for solubilizing surfactant, but polyols such as those containing from about 2 to about 6 carbon atoms and from about 2 to about 6 hydroxy groups (e.g., propylene glycol, ethylene glycol, glycerine, and 1,3-propanediol) can also be used.
  • polyols such as those containing from about 2 to about 6 carbon atoms and from about 2 to about 6 hydroxy groups (e.g., propylene glycol, ethylene glycol, glycerine, and 1,3-propanediol) can also be used.
  • the laundry detergent compositions of the present invention will preferably be formulated such that during use in aqueous cleaning operations, the wash water will have a pH of between about 6.5 and about 11, preferably between about 7.5 and about 10.5.
  • Liquid product formulations preferably have a pH between
  • This invention further provides a method for cleaning sub ⁇ strates, such as fibers, fabrics, hard surfaces, skin, etc., by contacting said substrate with a detergent composition containing the nonionic surfactant system of the present invention, wherein the weight ratio of polyhydroxy fatty acid amide to additional surfactant in the nonionic surfactant system is in the range of from about 1:5 to about 5:1, in the presence of a solvent such as water or a water-miscible solvent (e.g., primary and secondary alcohols). Agitation is preferably provided for enhancing cleaning. Suitable means for providing agitation include rubbing by hand preferably with the aid of a brush, or other cleaning device, automatic laundry washing machines, automatic dishwashers, etc.
  • EXPERIMENTAL This exemplifies a process for making a N-methyl, 1-deoxy- glucityl lauramide surfactant for use herein.
  • one suitable apparatus for use herein comprises a three-liter four-necked flask fitted with a motor-driven paddle stirrer and a thermometer of length sufficient to contact the reaction medium.
  • the other two necks of the flask are fitted with a nitrogen sweep and a wide-bore side- arm (caution: a wide-bore side-arm is important in case of very rapid methanol evolution) to which is connected an efficient collecting condenser and vacuum outlet.
  • the latter is connected to a nitrogen bleed and vacuum gauge, then to an aspirator and a trap.
  • a 500 watt heating mantle with a variable transformer temperature controller (“Variac”) used to heat the reaction is so placed on a lab-jack that it may be readily raised or lowered to further control temperature of the reaction.
  • N-methylglucamine 195 g., 1.0 mole, Aldrich, M4700-0
  • methyl laurate Procter & Gamble CE 1270, 220.9 g., 1.0 mole
  • the solid/liquid mixture is heated with stirring under a nitrogen sweep to form a melt (approximately 25 minutes).
  • catalyst anhydrous powdered sodium carbonate, 10.5 g., 0.1 mole, J. T. Baker
  • reaction temperature is held at 150* C by adjusting the Variac and/or by raising or lowering the mantle.
  • a surfactant paste is initially formed by combining any ° desired surfactants with water and alcohol.
  • the surfactants contained in this surfactant paste include the polyhydroxy fatty acid amides of the present invention. Ideally the surfactant paste should be pumpable at room or elevated temperatures.
  • non-aqueous solvents, the surfactant paste or 5 solution, melted fatty acids, aqueous solutions of polycarboxylate builders and other salts, aqueous ethoxylated tetraethylenepent ⁇ amine, buffering agents, caustic, and water are combined in a mixing vessel.
  • the pH is adjusted using either an aqueous citric acid solution or sodium hydroxide solution to a level of about 0 8.5.
  • the final ingredients such as soil release agents, enzymes, colorants and perfume, are added. The resulting mixture is stirred until a single phase compositions is obtained.
  • Examples of heavy-duty liquid detergent compositions contain ⁇ ing an alkylpolysaccharide as the additional nonionic surfactant in the nonionic surfactant systems are as follows. These examples are intended for wash temperatures below about 50°C, and a pre ⁇ ferred usage concentration of about 2,000 ppm, on a wash water weight basis, and are prepared in the same manner as the composi ⁇ tions of Examples 1-10.
  • An alternate method for preparing the polyhydroxy fatty acid amides used herein is as follows.
  • a reaction mixture consisting of 84.87g. fatty acid methyl ester (source: Procter & Gamble methyl ester CE1270), 75g. N-methyl-D-glucamine (source: Aldrich Chemical Company M4700-0), 1.04g. sodium methoxide (source: Aldrich Chemical Company 16,499-2), and 68.51g. methyl alcohol is used.
  • the reaction vessel comprises a standard reflux set-up fitted with a drying tube, condenser and stir bar. In this procedure, the N-methyl glucamine is combined with methanol with stirring under argon and heating is begun with good mixing (stir bar; reflux).
  • the ester and sodium methoxide catalyst are added. Samples are taken periodically to monitor the course of the reaction, but it is noted that the solution is completely clear by 63.5 minutes. It is judged that the reaction is, in fact, nearly complete at that point.
  • the reaction mixture is maintained at reflux for 4 hours. After removal of the methanol, the recovered crude product weighs 156.16 grams. After vacuum drying and purification, an overall yield of 106.92 grams purified product is recovered. However, percentage yields are not calculated on this basis, inasmuch as regular sampling throughout the course of the reaction makes an overall percentage yield value meaningless.
  • the reaction can be carried out at 80% and 90% reactant concentrations for periods up to 6 hours to yield products with extremely small by-product formation.
  • polyhydroxy fatty acid amides are, by virtue of their amide bond, subject to some instability under highly basic or highly acidic conditions. While some decomposition can be tolerated, it is preferred that these materials not be subjected to pH's above about 11, preferably 10, nor below about 3 for unduly extended periods. Final product pH (liquids) is typically 7.0-9.0.
  • the detergent formulator will recognize that it is a simple and convenient matter to use an acid which provides an anion that is otherwise useful and desirable in the 5 finished detergent composition.
  • citric acid can be used for purposes of neutralization and the resulting citrate ion (ca. 1%) be allowed to remain with a ca. 40% polyhydroxy fatty acid amide slurry and be pumped into the later manufacturing stages of the overall detergent-manufacturing process.
  • the acid 10 forms of materials such as oxydisuccinate, nitrilotriacetate, ethylenediaminetetraacetate, tartrate/succinate, and the like, can be used similarly.
  • the polyhydroxy fatty acid amides derived from coconut alkyl fatty acids are more soluble than their i5 tallow alkyl (predominantly C 16 -C 18 ) counterparts. Accordingly, the C 12 -C 14 materials are somewhat easier to formulate in liquid compositions, and are more soluble in cool-water laundering baths. However, the C 16 -C 18 materials are also quite useful, especially under circumstances where warm-to-hot wash water is used. Indeed,
  • the C 16 -C 1B materials may be better detersive surfactants than their C 12 -C 1 counterparts. Accordingly, the formulator may wish to balance ease-of-manufacture vs. performance when selecting a particular polyhydroxy fatty acid amide for use in a given formulation.
  • solubility of the polyhydroxy fatty acid amides can be increased by having points of unsaturation and/or chain branching in the fatty acid moiety.
  • materials such as the polyhydroxy fatty acid amides derived from oleic acid and iso-stearic acid are more soluble than their
  • polyhydroxy fatty acid amides prepared from disaccharides, trisaccharides, etc. will ordinarily be greater than the solubility of their monosaccharide-derived counterpart materials. This higher solubility can be of particu- " lar assistance when formulating liquid compositions.
  • polyhydroxy fatty acid amides wherein the polyhydroxy group is derived from maltose appear to function especially well as deter ⁇ gents when used in combination with conventional alkylbenzene sulfonate ("LAS") surfactants.
  • LAS alkylbenzene sulfonate
  • the polyhydroxy fatty acid amides can be manufactured not only from the purified sugars, but also from hydrolyzed starches, e.g., corn starch, potato starch, or any other convenient plant- derived starch which contains the mono-, di-, etc. saccharide desired by the formulator. This is of particular importance from the economic standpoint. Thus, "high glucose” corn syrup, "high maltose” corn syrup, etc. can conveniently and economically be used. De-lignified, hydrolyzed cellulose pulp can also provide a raw material source for the polyhydroxy fatty acid amides.
  • polyhydroxy fatty acid amides derived from the higher saccharides such as maltose, lactose, etc.
  • the more soluble polyhydroxy fatty acid amides can help solubilize their less soluble counterparts, to varying degrees.
  • the formulator may elect to use a raw material comprising a high glucose corn syrup, for example, but to select a syrup which contains a modicum of maltose (e.g., 1% or more).
  • the resulting mixture of polyhydroxy fatty acids will, in general, exhibit more preferred solubility properties over a broader range of temperatures and concentrations than would a "pure" glucose- derived polyhydroxy fatty acid amide.
  • the polyhydroxy fatty acid amides prepared from mixed sugars can offer very substantial advantages with respect to performance and/or ease-of-formulation.
  • some loss of grease removal performance may be noted at fatty acid maltamide levels above about 25% and some loss in sudsing above about 33% (said percentages being the percentage of maltamide-derived polyhydroxy fatty acid amide vs. glucose-derived polyhydroxy fatty acid amide in the mixture). This can vary somewhat, depending on the chain length of the fatty acid moiety.
  • the formulator electing to use such mixtures may find it advantageous to select polyhydroxy fatty acid amide mixtures which contain ratios of monosaccharides (e.g., glucose) to di- and higher saccharides (e.g., maltose) from about 4:1 to about 99:1.
  • monosaccharides e.g., glucose
  • di- and higher saccharides e.g., maltose
  • the formulator of, for example, solid, typically granular, detergent compositions may find it convenient to run the process at 30 * C-90'C in solvents which comprise ethoxylated alcohols, such as the ethoxylated (EO 3-8) C 12 -C 14 alcohols, such as those available as NEODOL 23 E06.5 (Shell).
  • ethoxylated alcohols such as the ethoxylated (EO 3-8) C 12 -C 14 alcohols, such as those available as NEODOL 23 E06.5 (Shell).
  • EO 3-8 ethoxylated (EO 3-8) C 12 -C 14 alcohols, such as those available as NEODOL 23 E06.5 (Shell).
  • ethoxylates it is preferred that they not contain substantial amounts of unethoxylated alcohol and, most preferably, not contain substantial amounts of mono-ethoxylated alcohol.
  • T designation.
  • the industrial scale reaction sequence for preparing the preferred acyclic polyhydroxy fatty acid amides will comprise: Step 1 - preparing the N-alkyl polyhydroxy amine derivative from the desired sugar or sugar mixture by formation of an adduct of the N-alkyl amine and the sugar, followed by reaction with hydrogen in the presence of a catalyst; followed by Step 2 - reacting the aforesaid polyhydroxy amine with, preferably, a fatty ester to form an amide bond.
  • Step 2 of the reaction sequence can be prepared by various art-disclosed processes, the following process is convenient and makes use of economical sugar syrup as the raw material. It is to be understood that, for best results when using such syrup raw materials, the manufacturer should select syrups that are quite light in color or, preferably, nearly colorless ("water-white").
  • the Gardner Color for the adduct is much worse as the temperature is raised above about 30*C and at about 50'C, the time that the adduct has a Gardner Color below 7 is only about 30 minutes. For longer reaction, and/or holding times, the temperature should be less than about 20*C.
  • the Gardner Color should be less than about 7, and preferably less than about 4 for good color glucamine.
  • the time to reach substantial equilibrium concentration of the adduct is shortened by the use of higher ratios of amine to sugar.
  • equilibrium is reached in about two hours at a reaction temperature of about 30*C.
  • the time is at least about three hours.
  • the combination of amine:sugar ratio; reaction temperature; and reaction time is selected to achieve substantially equilibrium conversion, e.g., more than about 90%, preferably more than about 95%, even more preferably more than about 99%, based upon the sugar, and a color that is less than about 7, preferably less than about 4, more preferably less than about 1, for the adduct.
  • substantially equilibrium conversion e.g., more than about 90%, preferably more than about 95%, even more preferably more than about 99%, based upon the sugar, and a color that is less than about 7, preferably less than about 4, more preferably less than about 1, for the adduct.
  • the starting sugar material must be very near colorless in order to consistently have adduct that is acceptable.
  • the adduct is sometimes acceptable and sometimes not accept ⁇ able.
  • the Gardner Color is above 1 the resulting adduct is unacceptable.
  • the better the initial color of the sugar, the better is the color of the adduct. ⁇ . Hvdrooen Reaction - Adduct from the above having a Gardner Color of 1 or less is hydrogenated according to the following procedure.
  • the resulting product in each case is greater than about 95% N-methyl glucamine; has less than about 10 ppm Ni based upon the glucamine; and has a solution color of less than about Gardner 2.
  • the crude N-methyl glucamine is color stable to about 140'C for a short exposure time.
  • adduct that has low sugar content (less than about 5%, preferably less than about 1%) and a good color (less than about 7, preferably less than about 4 Gardner, more preferably less than about 1).
  • adduct is prepared starting with about 159 g of about 50% methylamine in water, which is purged and shielded with N 2 at about 10-20'C. About 330 g of about 70% corn syrup (near water-white) is degassed with N 2 at about 50*C and is added slowly to the methylamine solution at a temperature of less than about 20 * C. The solution is mixed for about 30 minutes to give about 95% adduct that is a very light yellow solution. About 190 g of adduct in water and about 9 g of United Catalyst G49B Ni catalyst are added to a 200 ml autoclave and purged three times with H 2 at about 20 * C.
  • the H 2 pressure is raised to about 200 psi and the temperature is raised to about 50 ⁇ C.
  • the pressure is raised to 250 psi and the temperature is held at about 50-55'C for about three hours.
  • the product, which is about 95% hydrogenated at this point, is then raised to a temperature of about 85"C for about 30 minutes and the product, after removal of water and evaporation, is about 95% N-methyl glucamine, a white powder. It is also important to minimize contact between adduct and catalyst when the H 2 pressure is less than about 1000 psig to minimize Ni content in the glucamine.
  • the nickel content in the N-methyl glucamine in this reaction is about 100 ppm as compared to the less than 10 ppm in the previous reaction.
  • the following reactions with H 2 are run for direct comparison of reaction temperature effects.
  • Adduct for use in making glucamine is prepared by combining about 420 g of about 55% glucose (corn syrup) solution (231 g glucose; 1.28 moles) (the solution is made using 99DE corn syrup from CarGill, the solution having a color less than Gardner 1) and 5 about 119 g of 50% methylamine (59.5 g MMA; 1.92 moles) (from Air Products).
  • the adduct is used for the hydrogen reaction right after making, or is stored at low temperature to prevent further degradation.
  • TM The glucamine adduct hydrogen reactions are as follows:
  • the preparation of the tallow (hardened) fatty acid amide of N-methyl maltamine for use in detergent compositions according to this invention is as follows.
  • Step 1 - Reactants Maltose onohydrate (Aldrich, lot 01318KW); methylamine (40 wt% in water) (Aldrich, lot 03325TM); Raney nickel, 50% slurry (UAD 52-73D, Aldrich, lot 12921LW).
  • the reactants are added to glass liner (250 g maltose, 428 g methylamine solution, 100 g catalyst slurry - 50 g Raney Ni) and placed in 3 L rocking autoclave, which is purged with nitrogen (3X500 psig) and hydrogen (2X500 psig) and rocked under H 2 at room temperature over a weekend at temperatures ranging from 28*C to 50 ⁇ C.
  • the crude reaction mixture is vacuum filtered 2X through a glass microfiber filter with a silica gel plug.
  • the filtrate is concentrated to a viscous material.
  • the final traces of water are azetroped off by dissolving the material in methanol and then removing the ethanol/water on a rotary evaporator.
  • a silica gel slurry in 100% methanol is loaded into a funnel and washed several times with 100% methanol.
  • a concentrated sample of the product (20 g in 100 ml of 100% methanol) is loaded onto the silica gel and eluted several times using vacuum and several methanol washes.
  • the collected eluant is evaporated to dryness (rotary evaporator). Any remaining tallow ester is removed by trituration in ethyl acetate overnight, followed by filtration. The filter cake is vacuum dried overnight.
  • the product is the tallowalkyl N-methyl maltamide.
  • Step 1 of the foregoing reaction sequence can be conducted using commercial corn syrup comprising glucose or mixtures of glucose and, typically, 5%, or higher, maltose.
  • the resulting polyhydroxy fatty acid amides and mixtures can be used in any of the detergent compositions herein.
  • Step 2 of the foregoing reaction sequence can be carried out in 1,2-propylene glycol or NEODOL.
  • the propylene glycol or NEODOL need not be removed from the reaction product prior to its use to formulate detergent compositions.
  • the methoxide catalyst can be neutralized by citric acid to provide sodium citrate, which can remain in the polyhydroxy fatty acid amide.
  • the compositions herein can contain more or less of various suds control agents.
  • various suds control agents For dishwashing high sudsing is desirable so no suds control agent will be used.
  • a wide variety of suds control agents are known in the art and can be routinely selected for use herein. Indeed, the selection of suds control agent, or mixtures of suds control agents, for any specific detergent composition will depend not only on the presence and amount of polyhydroxy fatty acid amide used therein, but also on the other surfactants present in the formulation.
  • silicone-based suds control agents of various types are more efficient (i.e., lower levels can be used) than various other types of suds control agents.
  • the silicone suds control agents available as X2-3419 and Q2-3302 (Dow Corning) are particularly useful herein.
  • the formulator of fabric laundering compositions which can advantageously contain soil release agent has a wide variety of known materials to choose from (see, for example, U.S. Patents 3,962,152; 4,116,885; 4,238,531; 4,702,857; 4,721,580 and 4,877,896).
  • Additional soil release materials useful herein include the nonionic oligomeric esterification product of a reaction mixture comprising a source of C 1 -C 4 alkoxy-terminated polyethoxy units (e.g., CH 3 [0CH 2 CH 2 ] 16 0H), a source of tere- phthaloyl units (e.g., dimethyl terephthalate); a source of poly(oxyethylene)oxy units (e.g., polyethylene glycol 1500); a source of oxyiso-propyleneoxy units (e.g., 1,2-propylene glycol); and a source of oxyethyleneoxy units (e.g., ethylene glycol) especially wherein the mole ratio of oxyethyleneoxy units:oxyiso- propyleneoxy units is at least about 0.5:1.
  • a source of C 1 -C 4 alkoxy-terminated polyethoxy units e.g., CH 3 [0CH 2 CH 2 ] 16 0H
  • l ( C ) lk l i ll h l y are each integers from about 6 to about 100; m is an integer of from about 0.75 to about 30; n is an integer from about 0.25 to about 20; and R 2 is a mixture of both H and CH 3 to provide a mole ratio of oxyethyleneoxy:oxyisopropyleneoxy of at least about 0.5:1.
  • soil release agent useful herein is of the general anionic type described in U.S. Patent 4,877,896, but with the condition that such agents be substantially free of monomers of the HOROH type wherein R is propylene or higher alkyl.
  • the soil release agents of U.S. Patent 4,877,896 can comprise, for example, the reaction product of dimethyl terephthalate, ethylene glycol, 1,2-propylene glycol and 3-sodiosulfobenzoic acid
  • these additional soil release agents can comprise, for example, the reaction product of dimethyl terephthalate, ethylene glycol, 5-sodiosulfoisophthalate and 3-sodiosulfobenzoic acid.
  • Such agents are preferred for use in granular laundry detergents.
  • the formulator may also determine that it is advantageous to include a non-perborate bleach, especially in heavy-duty granular laundry detergents.
  • a non-perborate bleach especially in heavy-duty granular laundry detergents.
  • peroxygen bleaches are avail ⁇ able, commercially, and can be used herein, but, of these, per ⁇ carbonate is convenient and economical.
  • the compositions herein can contain a solid percarbonate bleach, normally in the form of the sodium salt, incorporated at a level of from 3% to 20% by weight, more preferably from 5% to 18% by weight and most preferably from 8% to 15% by weight of the composition.
  • Sodium percarbonate is an addition compound having a formula corresponding to 2Na 2 C0 3 . 3H 2 0 2 , and is available commercially as a crystalline solid. Most commercially available material includes a low level of a heavy metal sequestrant such as EDTA,
  • the percarbonate can be incorporated into detergent compositions without additional protection, but preferred embodiments of the invention utilize a stable form of
  • silicate can also be used and a chelant such as one of those mentioned above can also be included in the coating.
  • the particle size range of the crystalline percarbonate is from 350 micrometers to 450 micrometers with a mean of approximately 400 micrometers. When coated, the crystals have a
  • the total level of iron, copper and manganese ions in the product should not exceed 25 ppm and preferably should be less than 20 ppm in order to avoid an unacceptably adverse effect on percarbonate stability.
  • lipase and cellulase enzymes can be protected from degradation by protease enzymes.
  • lipase stability is still relatively poor in the presence of alkylbenzene sulfonate (“LAS") surfactants.
  • LAS alkylbenzene sulfonate
  • liquid detergent compositions containing lipase, protease and cellulase enzymes, together. It is particu ⁇ larly challenging to provide such tertiary enzyme systems in stable liquid detergents together with an effective blend of detersive surfactants. Additionally, it is difficult to incorporate peroxidase and/or amylase enzymes stably in such compositions.
  • the liquid detergents herein preferably comprise binary mixtures of the AES and polyhydroxy fatty acid amides of the type disclosed herein. While minimal amounts of LAS can be present, it will be appreciated that the stability of the enzymes will be lessened thereby. Accordingly, it is preferred that the liquid compositions be substantially free (i.e., contain less than about 10%, preferably less than about 5%, more preferably less than about 1%, most preferably 0%) of LAS.
  • the present invention provides a liquid detergent composition comprising:
  • R 1 is H l t C x -C hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl, or a mixture thereof
  • R 2 is C 5 -C 31 hydrocarbyl
  • Z is a polyhydroxylhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to said chain, or an alkoxylated derivative thereof;
  • a nonionic surfactant especially about l%-20% of an alkoxylated C 12 -C 18 alcohol with 3-10 EO groups; and wherein the composition is substantially free of alkylbenzene sulfonate.
  • the water-soluble anionic surfactant herein preferably comprises (“AES”):
  • R0(A) m S0 3 M wherein R is an unsubstituted C 10 -C 24 alkyl or hydroxyalkyl ( ⁇ o-C 2 ) group, A is an ethoxy or propoxy unit, m is an integer greater than 0 and M is hydrogen or a cation.
  • R is an unsubstituted C 12 -C 18 alkyl group, A is an ethoxy unit, m is from about 0.5 to about 6, and M is a cation.
  • the cation is preferably a metal cation (e.g., sodium-preferred, potassium, lithium, calcium, magnesium, etc.) or an ammonium or substituted ammonium cation.
  • the ratio of the above surfactant ("AES”) to the polyhydroxy fatty acid amide herein be from about 1:2 to about 8:1, preferably about 1:1 to about 5:1, most preferably about 1:1 to about 4:1.
  • the liquid compositions herein may alternatively comprise polyhydroxy fatty acid amide, AES, and from about 0.5% to about 5% of the condensation product of C 8 -C 22 (preferably C 10 -C 20 ) linear alcohol with between about 1 and about 25, preferably between about 2 and about 18, moles of ethylene oxide per mole of alcohol.
  • the liquid compositions herein preferably have a pH in a 10% solution in water at 20 ⁇ C of from about 6.5 to about 11.0, preferably from about 7.0 to about 8.5.
  • the instant compositions preferably further comprise from about 0.1% to about 50% of detergency builder.
  • compositions preferably comprise from about 0.1% to about 20% of citric acid, or water-soluble salt thereof, and from about 0.1% to about 20% of a water-soluble succinate tartrate, especially the sodium salt thereof, and mixtures thereof, or from about 0.1% to about 20% by weight of oxydisuccinate or mixtures thereof with the aforesaid builders. 0.1%-50% of alkenyl succinate can also be used.
  • the preferred liquid compositions herein comprise from about 0.0001% to about 2%, preferably about 0.0001% to about 1%, most preferably about 0.001% to about 0.5%, on an active basis, of detersive enzyme.
  • detersive enzymes are preferably selected from the group consisting of protease (preferred), lipase (preferred), amylase, cellulase, peroxidase, and mixtures thereof.
  • Preferred are compositions with two or more classes of enzymes, most prefer ⁇ ably where one is a protease.
  • lipases of interest include Amano AKG and Bacillis Sp lipase (e.g., Solvay enzymes). Also, see the lipases described in EP A 0399681, published November 28, 1990, EP A 0 218272, published April 15, 1987 and PCT/DK 88/00177, published May 18, 1989, all incorporated herein by reference. Suitable fungal lipases include those producible by Humicola lanuginosa and Thermo yces lanuginosus.
  • lipase obtained by cloning the gene from Humicola lanuginosa and expressing the gene in Aspergi l lus oryzae, as described in European Patent Application 0258068, incorporated herein by reference, commercially available under the trade name LIPOLASE. From about 2 to about 20,000, preferably about 10 to about 6,000, lipase units of lipase per gram (LU/g) of product can be used in these compositions.
  • a lipase unit is that amount of lipase which produces 1 ⁇ mol of titratable butyric acid per minute in a pH stat, where pH is 7.0, temperature is 30 ⁇ C, and substrate is an emulsion tributyrin and gum arabic, in the presence of Ca ++ and NaCl in phosphate buffer.
  • EXAMPLES 18 A-C The following Examples illustrate light duty liquid detergent compositions which are especially adapted for dishwashing and other hard surface cleaning operations.
  • the surfactants comprise various alkyl ethoxy sulfate surfactants which, using standard terminology, are abbreviated to indicate their average degree of ethoxylation; thus C 12 _ 13 E0(0.8) sulfate indicates a sulfated mixed C 12 -C 13 alcohol fraction having an average degree of ethoxylation of 0.8.
  • These anionic ethoxy sulfates are preferably used in their Na+ or NH 4 + salt form.
  • the C 12 . 13 amine oxide is a mixed C 12 . 13 (average) dimethyl amine oxide.
  • the C 12 - 14 AP betaine is C 12 / 14 H 25 / 29 C0NH(CH 2 ) 3 N + (CH 3 ) 2 - CH 2 C0 2 H.
  • the C 12 . 14 AP sultaine is C 12 / 14 H 25 / 29 C0NH(CH 2 ) 3 N + - (CH 3 ) 2 CH 2 CH(0H)CH 2 S0 3 H.
  • the C 12 . 14 DM betaine is C 12 / 14 H 25 / 29 N+- (CH 3 ) 2 CH 2 C0 2 H.
  • the ethoxylated nonionic surfactant designated Cg-iEOf ⁇ ) refers to Cg-C ⁇ alcohols ethoxylated with an average of 8 moles of ethylene oxide.
  • the Ca ++ and Mg ++ cations are conven ⁇ iently introduced into the compositions as CaCl 2 and MgCl 2 .
  • the balance of the compositions comprises water and citrate/propylene glycol present in the glucamide surfactant (1-5%) and 1-3% cumene sulfonate or xylene sulfonate hydrotrope.
  • the pH is typically 6.8-7.4 (NH 4 + salts) or 7-8.2 (Na+ salts).
  • a liquid laundry detergent composition suitable for use at the relatively high concentrations common to front-loading auto ⁇ matic washing machines, especially in Europe, and over a wide range of temperatures is as follows.
  • Amylase from NOVO; percentage at 300 KNU/g. ⁇ Lipase, from NOVO; percentage at 100 KLU/g. 5 Cellulase from NOVO; percentage at 5000 CEVU/1. 6 AvaiTable from Monsanto. 7 From BASF as LUTENS0L P6105. ⁇ BLANKOPHOR CPG766, Bayer. 9 Silane corrosion inhibitor, available as A1130 from Union Carbide or DYNASYLAN TRIAMINO from H ⁇ ls.
  • Silicone suds control agent available as Q2-3302 from Dow Corning.
  • fatty acid is topped palm kernel, comprising 12% oleic and 2% each of stearic and linoleic.
  • a granular laundry detergent composition suitable for use at the relatively high concentrations common to front-loading automatic washing machines, especially in Europe, and over a wide range of temperatures is as follows. In g redient Wt. %
  • • ⁇ OKALAN is sodium poly-acrylate/maleate available from Hoechst. 2 Monsanto brand of pentaphosphonomethyl diethylenetriamine. 3 0ptical brightener available from Ciba Geigy. Trade name FINNFIX available from Metasaliton. 5 LIP0LASE lipolytic enzyme from NOVO. 6 SAVINASE protease enzyme from NOVO. 7 X2-3419 is a silicone suds suppressor available from Dow Corning.
  • the procedure for preparing the granules comprises various tower-drying, agglomerating, dry-additions, etc., as follows. The percentages are based on the finished composition. A. Crutched and Blown Through the Tower
  • B. Surfactant Agglomerates Bl. Agglomeration of Sodium Salt.of Tallow Alkyl Sulfate and Sodium Salt of C-, ? -*,* ⁇ . E0(3) Sulfate Pastes - A 50% active paste of tallow alkyl sulfate and a 70% paste of C 12 -C 15 EO(3) sulfate are agglomerated with Zeolite A and sodium carbonate according to the following formula (contribution to the detergent formulation after the drying of the agglomerate).
  • a surfactant mixture of 20% DOBANOL C 12 . 15 E0(3) and 80% C 16 -C 18 N-methyl glucose amide is obtained and coagglomerated with 10% sodium carbonate.
  • the above particle is then coagglomerated with a high active paste (70%) of a sodium salt of C 1 -C 15 alkyl sulfate and
  • Ci 6 -C 18 N-methyl glucose amide Ci 6 -C 18 N-methyl glucose amide.
  • the overall formulation of this particle (contribution to the detergent formulation after the drying of the agglomerate) is: C 16 -C 18 N-methyl glucose amide 4.1% DOBANOL C 12 . 15 E0(3) 0.94%
  • the silicone suds suppressor X2-3419 (95%-97% high molecular weight starch; 3%-5% hydrophobic silica) ex Dow Corning is coagglomerated with Zeolite A (2-5 ⁇ size), starch and stearyl alcohol binder.
  • This particle has the following formulation: Zeolite A 0.22%
  • the detergent preparation exhibits excellent solubility, superior performance and excellent suds control when used in European washing machine, e.g., using 85 g detergent in a AEG- brand washing machine in 30 ⁇ C, 40 * C, 60 ⁇ C and 90*C cycles.
  • the fatty acid glucamide surfactant can be replaced by an equivalent amount of the malt- amide surfactant, or mixtures of glucamide/ altamide surfactants derived from plant sugar sources.
  • the use of ethanolamides appears to help cold temperature stability of the finished formulations.
  • the use of sulfobetaine (aka "sultaine") surfactants provides superior sudsing.
  • the formulator of high sudsing compositions will desirably avoid the introduction of suds- suppressing amounts of such fatty acids into high sudsing composi ⁇ tions with the polyhydroxy fatty acid amides, and/or avoid the formation of C 1 and higher fatty acids on storage of the finished compositions.
  • One simple means is to use C 12 ester reactants to prepare the polyhydroxy fatty acid amides herein. Fortunately, the use of amine oxide or sulfobetaine surfactants can overcome some of the negative sudsing effects caused by the fatty acids.
  • anionic optical brighteners to liquid detergents containing relatively high concentrations (e.g., 10% and greater) of anionic or polyanionic substituents such as the polycarboxylate builders may find it useful to pre-mix the bright ⁇ ener with water and the polyhydroxy fatty acid amide, and then to add the pre-mix to the final composition.
  • Polyglutamic acid or polyaspartic acid dispersants can be usefully employed with zeolite-built detergents.
  • AE fluid or flake and DC-544 are other examples of useful suds control agents herein.

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Abstract

Systèmes tensioactifs non ioniques comprenant: (a) un ou plusieurs amides d'acides gras de polyhydroxy de formule (I), dans laquelle R1 est H, un hydrocarbyle C¿1?-C4, 2-hydroxy éthyle, 2-hydroxy propyle, ou des mélanges de ces composés, R?2¿ est un hydrocarbyle C¿5?-C31, et Z est un polyhydroxy hydrocarbyle possédant une chaîne hydrocarbyle linéaire présentant au moins trois groupes hydroxyle reliés directement à la chaîne, ou un dérivé alcoxylé de ce composé; et (b) un ou plusieurs tensioactifs non ioniques supplémentaires. Le rapport pondéral entre l'amide d'acide gras polyhydroxy (a) et le tensioactif non ionique supplémentaire (b) se situe entre environ 1:5 et environ 5:1. La présente invention permet également de produire des compositions détergentes contenant les systèmes tensioactifs non ioniques susmentionnées. Lorsqu'ils sont inclus dans des compositions détergentes pour lessive, ces systèmes tensioactifs non ioniques améliorent de manière inattendue le pouvoir détachant desdites compositions et permettent de traiter des taches d'huile ou de graisse dans une vaste gamme de conditions de lessive. Est également décrit un procédé permettant d'accroître le pouvoir détachant des compositions détergentes par l'incorporation dans ces compositions des systèmes tensioactifs non ioniques susmentionnés.
PCT/US1991/006980 1990-09-28 1991-09-25 Systemes tensioactifs non ioniques contenant des amides d'acides gras de polyhydroxy et un ou plusieurs tensioactifs non ioniques supplementaires WO1992006160A1 (fr)

Priority Applications (9)

Application Number Priority Date Filing Date Title
DE69127449T DE69127449T2 (de) 1990-09-28 1991-09-25 Polyhydroxyfettsäureamide und ein oder mehrere zusätzliche nichtionische tenside enthaltende nichtionische tensidsysteme
SK24493A SK24493A3 (en) 1990-09-28 1991-09-25 Nonionic sulphactany systems containing polyhydroxy fatty acid amides and one or more additional nonionic surfactants
AU86469/91A AU664356B2 (en) 1990-09-28 1991-09-25 Nonionic surfactant systems containing polyhydroxy fatty acid amides and one or more additional nonionic surfactants
EP91917564A EP0550606B1 (fr) 1990-09-28 1991-09-25 Systemes tensioactifs non ioniques contenant des amides d'acides gras de polyhydroxy et un ou plusieurs tensioactifs non ioniques supplementaires
CS93432A CZ43293A3 (en) 1990-09-28 1991-09-25 Process for improving dirt-removing properties of a cleansing preparation containing one or a plurality of non-ionogenic detergent surface-active agents and optionally auxiliary detergent agents
BR919106934A BR9106934A (pt) 1990-09-28 1991-09-25 Sistemas tensoativos nao-jonicos contendo amidas de acidos graxos poliidroxi e um ou mais tensoativos nao-ionicos adicionais
JP03516294A JP3119873B2 (ja) 1990-09-28 1991-09-25 ポリヒドロキシ脂肪酸アミドと１種以上の追加の非イオン界面活性剤とを含有する非イオン界面活性剤系
NO93931019A NO931019L (no) 1990-09-28 1993-03-22 Ikke-ioniske overflateaktive middelsystemer inneholdende polyhydroksy-fettsyreamider og et eller flere ytterligere ikke-ioniske overflateaktive midler
FI931360A FI931360A (fi) 1990-09-28 1993-03-26 System foer icke-joniska ytaktiva substanser, vilka innehaoller polyhydroxifettsyraamider och en eller flere ytterligare icke-jonisk ytaktiv substans

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US755,894 1976-12-30
US58976090A 1990-09-28 1990-09-28
US589,760 1990-09-28
US73037591A 1991-07-11 1991-07-11
US730,375 1991-07-11
US75589491A 1991-09-06 1991-09-06

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AR (1) AR244322A1 (fr)
AT (1) ATE157392T1 (fr)
AU (1) AU664356B2 (fr)
BR (1) BR9106934A (fr)
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DE (1) DE69127449T2 (fr)
FI (1) FI931360A (fr)
HU (1) HU213522B (fr)
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WO1994005680A1 (fr) * 1992-09-03 1994-03-17 Henkel Kommanditgesellschaft Auf Aktien Agents dispersants
EP0593406A1 (fr) * 1992-10-13 1994-04-20 The Procter & Gamble Company Compositions détergentes liquides non aqueuses
WO1994012511A1 (fr) * 1992-11-25 1994-06-09 Unilever Plc Aldonamides et leur utilisation comme tensioactifs
WO1994021226A1 (fr) * 1993-03-24 1994-09-29 Henkel Kommanditgesellschaft Auf Aktien Melanges de detergents presentant des caracteristiques d'avivage ameliorees
WO1994021771A1 (fr) * 1993-03-24 1994-09-29 Henkel Kommanditgesellschaft Auf Aktien Melanges de detergents
DE4323253C1 (de) * 1993-07-12 1995-01-05 Henkel Kgaa Verwendung von Fettsäure-N-alkylpolyhydroxyalkylamiden als Klarspülmittel für die maschinelle Reinigung harter Oberflächen
WO1995007968A1 (fr) * 1993-09-13 1995-03-23 The Procter & Gamble Company Compositions detergentes granulaires comprenant un tensioactif non ionique, et procede de fabrication de ces compositions
EP0673993A2 (fr) * 1994-03-23 1995-09-27 Amway Corporation Composition nettoyante liquide ou base tensio-active, procédé pour la fabrication et méthode de nettoyage
WO1996003482A1 (fr) * 1994-07-28 1996-02-08 The Procter & Gamble Company Procede de production de detergents granulaires et compositions de detergents comprenant un agent tensioactif non ionique
US5500155A (en) * 1994-03-18 1996-03-19 Henkel Kommanditgesellschaft Auf Aktien Detergent mixtures of fatty acid isethionate salts and fatty alcohols
WO1996013564A1 (fr) * 1994-10-28 1996-05-09 The Procter & Gamble Company Compositions non aqueuses comprenant des amides d'acides gras polyhydroxyles
WO1997000930A1 (fr) * 1995-06-21 1997-01-09 The Procter & Gamble Company Composes pour le lavage de la vaisselle a la main
WO1997002335A1 (fr) * 1995-07-04 1997-01-23 Henkel Kommanditgesellschaft Auf Aktien Concentres de tensioactifs non ioniques
DE19529590A1 (de) * 1995-08-11 1997-02-13 Henkel Kgaa Milde Detergensgemische
EP0776653A1 (fr) 1995-11-30 1997-06-04 Henkel Kommanditgesellschaft auf Aktien Compositions cosmétiques et/ou pharmaceutiques contenant des amides d'acides gras polyhydroxyle
EP0780464A2 (fr) 1995-12-21 1997-06-25 Henkel Kommanditgesellschaft auf Aktien Procédé pour la préparation des concentrés d'agents tensio-actifs de couleur claire à basse viscosité
US5698510A (en) * 1993-09-13 1997-12-16 The Procter & Gamble Company Process for making granular detergent compositions comprising nonionic surfactant
US5712235A (en) * 1993-09-15 1998-01-27 Henkel Kommanditgesellschaft Auf Aktien Bar soaps
US5741314A (en) * 1995-10-19 1998-04-21 Daly; Christopher Newton Embedded data link and protocol
EP0849354A1 (fr) * 1996-12-20 1998-06-24 Unilever Plc Compositions adoucissantes
WO1998032416A1 (fr) * 1997-01-27 1998-07-30 The Procter & Gamble Company Procede de demaquillage de la peau
US5789372A (en) * 1994-01-12 1998-08-04 Henkel Kommanditgesellschaft Auf Aktien Surfactant mixtures having improved surface-active properties
DE19749155A1 (de) * 1997-10-24 1999-05-20 Cheng Wen Lin Mehrzweck-Reinigungsmittel
WO1999025796A2 (fr) * 1997-11-18 1999-05-27 Unilever Plc Compositions detergentes en poudre contenant des activateurs de blanchiment du type glucamide
US5932535A (en) * 1995-12-21 1999-08-03 Henkel Kommanditgesellschaft Auf Aktien Process for the production of light-colored, low-viscosity surfactant concentrates
EP0984055A1 (fr) * 1998-09-04 2000-03-08 Clariant GmbH Mélanges solides de tensioactifs contenant des polyhydroxyamides d'acides gras
EP1078978A1 (fr) * 1999-08-24 2001-02-28 Clariant GmbH Mélanges de tensioactifs de N-alkyl polyhydroxyamides et amides alcoxylés d'acides gras
US6264961B1 (en) 1995-09-11 2001-07-24 Henkel Kommanditgesellschaft Auf Aktien Oil-water emulsifiers
US6339057B1 (en) * 1997-04-14 2002-01-15 Stepan Company High foaming detergent composition having a non-ionic surfactant base
US6471945B2 (en) 2000-03-10 2002-10-29 Warner-Lambert Company Stain removing chewing gum and confectionery compositions, and methods of making and using the same
US6485739B2 (en) 2000-03-10 2002-11-26 Warner-Lambert Company Stain removing chewing gum and confectionery compositions, and methods of making and using the same
US6630437B1 (en) 1998-12-16 2003-10-07 Unilever Home & Personal Care Usa , Division Of Conopco, Inc. Transparent/translucent liquid compositions in clear bottles comprising colorant and fluorescent dye or UV absorber
US6846796B2 (en) 2000-04-15 2005-01-25 Cognis Deutschland Gmbh & Co. Kg Method for producing non-ionic tenside granulates
DE102005025933B3 (de) * 2005-06-06 2006-07-13 Centrotherm Photovoltaics Gmbh + Co. Kg Dotiergermisch für die Dotierung von Halbleitern
US7390518B2 (en) 2003-07-11 2008-06-24 Cadbury Adams Usa, Llc Stain removing chewing gum composition
US7445769B2 (en) 2002-10-31 2008-11-04 Cadbury Adams Usa Llc Compositions for removing stains from dental surfaces and methods of making and using the same
WO2009076201A1 (fr) * 2007-12-07 2009-06-18 Fontana Technology Procédé et composition pour le nettoyage des plaquettes
US7641892B2 (en) 2004-07-29 2010-01-05 Cadburry Adams USA, LLC Tooth whitening compositions and delivery systems therefor
EP2157162A1 (fr) 2008-08-13 2010-02-24 The Procter and Gamble Company Composition de blanchiment particulaire comportant des enzymes
US7727565B2 (en) 2004-08-25 2010-06-01 Cadbury Adams Usa Llc Liquid-filled chewing gum composition
WO2011144921A2 (fr) 2010-05-20 2011-11-24 Reckitt & Colman (Overseas) Limited Composition et procédé associé
US8133476B2 (en) 2006-04-05 2012-03-13 Cadbury Adams Usa Llc Calcium phosphate complex and salts in oral delivery systems
US8252269B2 (en) 2006-04-05 2012-08-28 Cadbury Adams Usa, Llc Impact of calcium phosphate complex on dental caries
US9011946B2 (en) 2011-04-29 2015-04-21 Intercontinental Great Brands Llc Encapsulated acid, method for the preparation thereof, and chewing gum comprising same
US9198448B2 (en) 2005-02-07 2015-12-01 Intercontinental Great Brands Llc Stable tooth whitening gum with reactive ingredients
US9271904B2 (en) 2003-11-21 2016-03-01 Intercontinental Great Brands Llc Controlled release oral delivery systems
US20210230511A1 (en) * 2020-01-28 2021-07-29 The Procter & Gamble Company Cleaning product

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JPH0625522U (ja) * 1992-08-31 1994-04-08 三菱重工業株式会社 ２サイクルエンジン
WO2013178670A2 (fr) * 2012-05-30 2013-12-05 Clariant International Ltd. Utilisation de n-méthyl-n-acylglucamines comme stabilisateurs au froid dans des solutions tensioactives
JP6220652B2 (ja) * 2013-11-26 2017-10-25 日華化学株式会社 医療器具用洗浄剤組成物
EP3241887A1 (fr) * 2016-08-01 2017-11-08 Clariant International Ltd Composition comprenant un éthoxylate d'alcool et de glucamide
US20190110472A1 (en) * 2017-10-12 2019-04-18 Clariant International, Ltd. Active ingredient compositions comprising n-alkenoyl-n-alkylglucamides and the use thereof
CN114191323B (zh) * 2021-12-24 2024-03-26 岳阳科罗德联合化学工业有限公司 一种Gemini谷氨酸氨基酸表面活性剂组合物及其制备方法和应用
WO2023128951A1 (fr) * 2021-12-27 2023-07-06 Eczacibasi Tuketim Urunleri Sanayi Ve Ticaret Anonim Sirketi Composition de détergent à lessive ayant une propriété d'adoucissement et détergent à lessive comprenant ladite composition

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EP0220676A1 (fr) * 1985-10-29 1987-05-06 Süddeutsche Zucker-Aktiengesellschaft Amides d'acides gras d'aminopolyols comme tensio-actifs non ionogènes
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EP0264615A1 (fr) * 1986-09-22 1988-04-27 Henkel Kommanditgesellschaft auf Aktien Agent de lavage ayant une teneur réduite en phosphate contenant d'acide gras d'amides-N alcoxylé
EP0285768A1 (fr) * 1987-04-08 1988-10-12 Hüls Aktiengesellschaft Utilisation de N-polyhydroxyalkyl d'amides d'acides gras comme agents épaississants pour systèmes tensio-actifs liquides aqueux

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EP0220676A1 (fr) * 1985-10-29 1987-05-06 Süddeutsche Zucker-Aktiengesellschaft Amides d'acides gras d'aminopolyols comme tensio-actifs non ionogènes
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Cited By (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994005680A1 (fr) * 1992-09-03 1994-03-17 Henkel Kommanditgesellschaft Auf Aktien Agents dispersants
EP0593406A1 (fr) * 1992-10-13 1994-04-20 The Procter & Gamble Company Compositions détergentes liquides non aqueuses
WO1994012511A1 (fr) * 1992-11-25 1994-06-09 Unilever Plc Aldonamides et leur utilisation comme tensioactifs
WO1994021226A1 (fr) * 1993-03-24 1994-09-29 Henkel Kommanditgesellschaft Auf Aktien Melanges de detergents presentant des caracteristiques d'avivage ameliorees
WO1994021771A1 (fr) * 1993-03-24 1994-09-29 Henkel Kommanditgesellschaft Auf Aktien Melanges de detergents
US5691300A (en) * 1993-07-12 1997-11-25 Henkel Kommanditgesellschaft Auf Aktien Rinse aids for the machine washing of hard surfaces
DE4323253C1 (de) * 1993-07-12 1995-01-05 Henkel Kgaa Verwendung von Fettsäure-N-alkylpolyhydroxyalkylamiden als Klarspülmittel für die maschinelle Reinigung harter Oberflächen
WO1995007968A1 (fr) * 1993-09-13 1995-03-23 The Procter & Gamble Company Compositions detergentes granulaires comprenant un tensioactif non ionique, et procede de fabrication de ces compositions
US5698510A (en) * 1993-09-13 1997-12-16 The Procter & Gamble Company Process for making granular detergent compositions comprising nonionic surfactant
US5712235A (en) * 1993-09-15 1998-01-27 Henkel Kommanditgesellschaft Auf Aktien Bar soaps
US5789372A (en) * 1994-01-12 1998-08-04 Henkel Kommanditgesellschaft Auf Aktien Surfactant mixtures having improved surface-active properties
US5500155A (en) * 1994-03-18 1996-03-19 Henkel Kommanditgesellschaft Auf Aktien Detergent mixtures of fatty acid isethionate salts and fatty alcohols
EP0673993A2 (fr) * 1994-03-23 1995-09-27 Amway Corporation Composition nettoyante liquide ou base tensio-active, procédé pour la fabrication et méthode de nettoyage
EP0673993A3 (fr) * 1994-03-23 1998-02-25 Amway Corporation Composition nettoyante liquide ou base tensio-active, procédé pour la fabrication et méthode de nettoyage
WO1996003482A1 (fr) * 1994-07-28 1996-02-08 The Procter & Gamble Company Procede de production de detergents granulaires et compositions de detergents comprenant un agent tensioactif non ionique
WO1996013564A1 (fr) * 1994-10-28 1996-05-09 The Procter & Gamble Company Compositions non aqueuses comprenant des amides d'acides gras polyhydroxyles
WO1997000930A1 (fr) * 1995-06-21 1997-01-09 The Procter & Gamble Company Composes pour le lavage de la vaisselle a la main
WO1997002335A1 (fr) * 1995-07-04 1997-01-23 Henkel Kommanditgesellschaft Auf Aktien Concentres de tensioactifs non ioniques
DE19529590A1 (de) * 1995-08-11 1997-02-13 Henkel Kgaa Milde Detergensgemische
DE19529590C2 (de) * 1995-08-11 1999-06-02 Henkel Kgaa Milde Haarshampoos
US6264961B1 (en) 1995-09-11 2001-07-24 Henkel Kommanditgesellschaft Auf Aktien Oil-water emulsifiers
US5741314A (en) * 1995-10-19 1998-04-21 Daly; Christopher Newton Embedded data link and protocol
EP0776653A1 (fr) 1995-11-30 1997-06-04 Henkel Kommanditgesellschaft auf Aktien Compositions cosmétiques et/ou pharmaceutiques contenant des amides d'acides gras polyhydroxyle
EP0780464A2 (fr) 1995-12-21 1997-06-25 Henkel Kommanditgesellschaft auf Aktien Procédé pour la préparation des concentrés d'agents tensio-actifs de couleur claire à basse viscosité
US5932535A (en) * 1995-12-21 1999-08-03 Henkel Kommanditgesellschaft Auf Aktien Process for the production of light-colored, low-viscosity surfactant concentrates
EP0849354A1 (fr) * 1996-12-20 1998-06-24 Unilever Plc Compositions adoucissantes
WO1998028390A1 (fr) * 1996-12-20 1998-07-02 Unilever Plc Compositions de produit d'assouplissement
WO1998032416A1 (fr) * 1997-01-27 1998-07-30 The Procter & Gamble Company Procede de demaquillage de la peau
US5942238A (en) * 1997-01-27 1999-08-24 The Procter & Gamble Company Method for removing make-up from skin
US6339057B1 (en) * 1997-04-14 2002-01-15 Stepan Company High foaming detergent composition having a non-ionic surfactant base
DE19749155A1 (de) * 1997-10-24 1999-05-20 Cheng Wen Lin Mehrzweck-Reinigungsmittel
WO1999025796A2 (fr) * 1997-11-18 1999-05-27 Unilever Plc Compositions detergentes en poudre contenant des activateurs de blanchiment du type glucamide
WO1999025796A3 (fr) * 1997-11-18 1999-07-29 Unilever Plc Compositions detergentes en poudre contenant des activateurs de blanchiment du type glucamide
US6165972A (en) * 1998-09-04 2000-12-26 Clariant Gmbh Solid surfactant mixtures comprising fatty acid polyhydroxyamides
EP0984055A1 (fr) * 1998-09-04 2000-03-08 Clariant GmbH Mélanges solides de tensioactifs contenant des polyhydroxyamides d'acides gras
US6630437B1 (en) 1998-12-16 2003-10-07 Unilever Home & Personal Care Usa , Division Of Conopco, Inc. Transparent/translucent liquid compositions in clear bottles comprising colorant and fluorescent dye or UV absorber
EP1078978A1 (fr) * 1999-08-24 2001-02-28 Clariant GmbH Mélanges de tensioactifs de N-alkyl polyhydroxyamides et amides alcoxylés d'acides gras
US6471945B2 (en) 2000-03-10 2002-10-29 Warner-Lambert Company Stain removing chewing gum and confectionery compositions, and methods of making and using the same
US6485739B2 (en) 2000-03-10 2002-11-26 Warner-Lambert Company Stain removing chewing gum and confectionery compositions, and methods of making and using the same
US6696044B2 (en) 2000-03-10 2004-02-24 Cadbury Adams Usa Llc Stain removing chewing gum and confectionery compositions, and methods of making and using the same
US6846796B2 (en) 2000-04-15 2005-01-25 Cognis Deutschland Gmbh & Co. Kg Method for producing non-ionic tenside granulates
US7445769B2 (en) 2002-10-31 2008-11-04 Cadbury Adams Usa Llc Compositions for removing stains from dental surfaces and methods of making and using the same
US7390518B2 (en) 2003-07-11 2008-06-24 Cadbury Adams Usa, Llc Stain removing chewing gum composition
US7641927B2 (en) 2003-07-11 2010-01-05 Cadbury Adams Usa, Llc Chewing gum and confectionery compositions containing a stain removing complex, and methods of making and using the same
US9271904B2 (en) 2003-11-21 2016-03-01 Intercontinental Great Brands Llc Controlled release oral delivery systems
US7641892B2 (en) 2004-07-29 2010-01-05 Cadburry Adams USA, LLC Tooth whitening compositions and delivery systems therefor
US7727565B2 (en) 2004-08-25 2010-06-01 Cadbury Adams Usa Llc Liquid-filled chewing gum composition
US9198448B2 (en) 2005-02-07 2015-12-01 Intercontinental Great Brands Llc Stable tooth whitening gum with reactive ingredients
DE102005025933B3 (de) * 2005-06-06 2006-07-13 Centrotherm Photovoltaics Gmbh + Co. Kg Dotiergermisch für die Dotierung von Halbleitern
US8043946B2 (en) 2005-06-06 2011-10-25 Centrotherm Photovoltaics Ag Mixture for doping semiconductors
US8133476B2 (en) 2006-04-05 2012-03-13 Cadbury Adams Usa Llc Calcium phosphate complex and salts in oral delivery systems
US8252269B2 (en) 2006-04-05 2012-08-28 Cadbury Adams Usa, Llc Impact of calcium phosphate complex on dental caries
EP2229243A4 (fr) * 2007-12-07 2012-11-21 Fontana Technology Procédé et composition pour le nettoyage des plaquettes
US8226773B2 (en) 2007-12-07 2012-07-24 Fontana Technology Method and composition for cleaning wafers
EP2229243A1 (fr) * 2007-12-07 2010-09-22 Fontana Technology Procédé et composition pour le nettoyage des plaquettes
US8496757B2 (en) 2007-12-07 2013-07-30 Fontana Technology Method for cleaning wafers using a polycarboxylate solution
WO2009076201A1 (fr) * 2007-12-07 2009-06-18 Fontana Technology Procédé et composition pour le nettoyage des plaquettes
US8343907B2 (en) 2008-08-13 2013-01-01 The Procter & Gamble Company Particulate bleaching composition comprising enzymes
EP2157162A1 (fr) 2008-08-13 2010-02-24 The Procter and Gamble Company Composition de blanchiment particulaire comportant des enzymes
WO2011144921A2 (fr) 2010-05-20 2011-11-24 Reckitt & Colman (Overseas) Limited Composition et procédé associé
US9011946B2 (en) 2011-04-29 2015-04-21 Intercontinental Great Brands Llc Encapsulated acid, method for the preparation thereof, and chewing gum comprising same
US9737082B2 (en) 2011-04-29 2017-08-22 Intercontinental Great Brands Llc Chewing gum composition comprising encapsulated acid
US20210230511A1 (en) * 2020-01-28 2021-07-29 The Procter & Gamble Company Cleaning product
US11753604B2 (en) * 2020-01-28 2023-09-12 The Procter & Gamble Company Cleaning product

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JPH06501505A (ja) 1994-02-17
DE69127449D1 (de) 1997-10-02
HU9300894D0 (en) 1993-07-28
DE69127449T2 (de) 1998-03-26
NZ240042A (en) 1995-08-28
HU213522B (en) 1997-07-28
EP0550606B1 (fr) 1997-08-27
CZ43293A3 (en) 1994-04-13
AU664356B2 (en) 1995-11-16
HUT64383A (en) 1993-12-28
AU8646991A (en) 1992-04-28
FI931360A0 (fi) 1993-03-26
AR244322A1 (es) 1993-10-29
ATE157392T1 (de) 1997-09-15
FI931360A (fi) 1993-03-26
BR9106934A (pt) 1994-01-25
JP3119873B2 (ja) 2000-12-25
TW224486B (fr) 1994-06-01
MX9101356A (es) 1992-05-04
CN1035829C (zh) 1997-09-10
CN1062163A (zh) 1992-06-24
EP0550606A1 (fr) 1993-07-14

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