EP0339120A1 - Isotropic laundry detergents - Google Patents

Isotropic laundry detergents Download PDF

Info

Publication number
EP0339120A1
EP0339120A1 EP19880106946 EP88106946A EP0339120A1 EP 0339120 A1 EP0339120 A1 EP 0339120A1 EP 19880106946 EP19880106946 EP 19880106946 EP 88106946 A EP88106946 A EP 88106946A EP 0339120 A1 EP0339120 A1 EP 0339120A1
Authority
EP
European Patent Office
Prior art keywords
weight percent
formula
alkyl
composition according
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP19880106946
Other languages
German (de)
French (fr)
Inventor
Ernest Bernarducci
Kenneth Allen Harrison
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
STWB Inc
Original Assignee
Sterling Drug Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US06/935,658 priority Critical patent/US4755327A/en
Application filed by Sterling Drug Inc filed Critical Sterling Drug Inc
Priority to EP19880106946 priority patent/EP0339120A1/en
Publication of EP0339120A1 publication Critical patent/EP0339120A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/75Amino oxides
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723Polyamines or polyalkyleneimines

Definitions

  • This invention relates to isotropic liquid laundry detergents containing polymeric quaternary ammonium salts in combination with one or more nonionic surfactants.
  • U.S. Patent 3,771,989 discloses poly­meric polyelectrolytes, useful as algicides, having the formula: where n is an integer from 4 to 40, with molecular weights ranging from 1,000 to 10,000, which are chemically desig­nated poly[oxyethylene(dimethyliminio)ethylene(dimethyl­iminio)ethylene dichloride]. As far as is presently known, compounds of this class are not known to have useful bactericidal properties nor are they known to be useful for incorporation in laundry detergents.
  • U.S. Patents 3,931,319; 4,001, 432 and 4,012,446 disclose so-called "capped” polymers useful as "microbiocidal” agents, which have linear polymeric quaternary chains terminated by quaternary ammonium moieties, having the formula: where X ⁇ is halide and "n is an integer from about 2 to about 30; where R′ and R ⁇ may be either (1) a primary or secondary alkyl radical having from 1 to 20 carbon atoms, (2) hydroxy or dihydroxy derivatives of R′ and R ⁇ , (3) benzyl, or (4) benzyl containing at least one alkyl group...; where Z consists of from one to three aliphatic divalent radicals, each of which has 2 to 10 carbon atoms, each aliphatic radical containing 0 to 2 double bonds and 0 to 2 hydroxy substituents" and where "R III , R IV and R V may be either (1) primary or secondary alkyl containing from 1 to 20 carbon atoms, or (2) hydroxy­
  • the compounds are said to be effective against bacteria and algae and to a lesser extend against fungi. They are also stated to be non-foaming, a property which is said to be important in anti-microbial agents used in products and processes where the generation of foam is undesirable.
  • U.S. Patent 4,091,113 discloses "ran­domly terminated” capped linear quaternary ammonium poly­mers prepared in the same manner as described in U.S. Patent 4,027,020 supra .
  • the quaternaries are said to be "uniquely excellent hair conditioning agents" which are "compatible in binary or tertiary systems with most of the lathering and cleansing surfactants used in hair conditioning consumer products".
  • the patentee states that 40% aqueous solutions are non-irritating to the skin and that 4% aqueous solutions are non-irritating to the eyes.
  • the quaternaries are described as being compatible with surfactants and emulsi­fiers of the cationic, nonionic, amine oxide, alkylol­amide, amphoteric, aminoacetic or ⁇ -aminopropionic acid and betaine or betaine salt classes.
  • the compositions are exemplified in Examples 28, 29 and 30 by formulations containing the polymeric quaternary which is produced by reaction of 1,4-bis-dimethylamino-2-butene, triethan­olamine and 1,4-dichloro-2-butene in water in combination with surfactants of the cationic (AMMONYX®4, i.e.
  • stearal­konium chloride -Example 30 nonionic (TERGITOL® 15-S-12, i.e. pareth-15-12 - Example 29), alkylolamide (ONYXOL® 42, i.e. stearyl diethanolamide - Example 30 and SUPER AMIDE® GR, i.e. cocoyldiethanolamide - Example 28), ampho­teric (MIRANOL® C-2M-SF, i.e. cocoamphocarboxypropionate and SANDOPAN® TFL, i.e. oleoamphopropylsulfonate - both Example 28) and anionic (MAPROFIX® 60S, i.e.
  • U.S. Patent 4,333,862 discloses, as one possible cationic surfactant in liquid detergent compositions containing an anionic, a cationic and a nonionic surfactant, polyammonium salts of the formula: where R3 is C8-C20 alkyl, alkenyl or aralkyl; each R4 is C1-C4 alkyl or hydroxyalkyl; n is from 1 to 6; and m is from 1 to 3.
  • polymeric linear quaternary ammonium salts of the structural types represented by those dis­closed in U.S. Patents 3,771,989; 3,931,319; 4,001,432; 4,012,446; 4,027,020 and 4,091,113 are not known to have been incorporated in laundry detergents.
  • polymeric quaternary ammonium salts of those classes when formulated in an aqueous medium with one or more nonionic surfactants, provide stable, isotropic liquid laundry detergents and sanitizer compositions having good detergency and bactericidal properties, which, in addition, are moderately irritating to the eyes and practically non-irritating to the skin.
  • the invention resides in stable, isotropic liquid laundry detergent and sanitizer composi­tions comprising: (A) a polymeric linear quaternary ammo­nium salt selected from the group consisting of a poly[oxy­ethylene)di-lower-alkyliminio)ethylene(di-lower-alkyliminio)-­ethylene dihalide] and a polymeric quaternary ammonium halide corresponding to formula IB hereinbelow; (B) one or more nonionic surfactants selected from the group consisting of the polyethylene glycol long chain alkyl ether, polyethylene glycol alkylphenyl ether, N-alkyl-­N,N-di-lower-alkylamine-N-oxide and alkyl polyglycoside classes; and (C) water.
  • A a polymeric linear quaternary ammo­nium salt selected from the group consisting of a poly[oxy­ethylene)di-lower-alkyli
  • the isotropic liquid laundry detergent and sanitizer compositions of the invention comprise: (A) a polymeric linear quaternary ammonium salt selected from the group consisting of a poly[oxy­ethylene)di-lower-alkyliminio)ethylene(di-lower-alkyl­iminio)ethylene dihalide] having the formula: where R1 is lower-alkyl having from one to four carbon atoms, a is an integer from 4 to 40, with an average value of 19, and X ⁇ is halide, and a polymeric quaternary ammonium halide having the formula: where R2 is hydroxy-lower-alkyl having from two to four carbon atoms, b is an integer from 27 to 57 and R1 and X ⁇ have the meanings given above; (B) one or more nonionic surfactants selected from the group consisting of a polyethylene glycol long chain alkyl ether having the formula: R4 OCH2CH2) c OH IIA where R4 is C
  • the polymeric quaternary ammonium salts of for­mulas IA and IB used to prepare the compositions of the invention are well known classes of compounds.
  • the poly­[oxyethylene)di-lower-alkyliminio)ethylene(di-lower-alkyl­iminio)ethylene dihalide] quaternaries of formula IA include, for example, poly[oxyethylene(dimethyliminio)­ethylene(dimethyliminio)ethylene dichloride] sold under the trade name BUSAN® 77 by Buckman Laboratories, Memphis, Tennessee as a 60% actives solution in water which is identified as WSCP (water soluble cationic polymer).
  • the polymeric quaternary ammonium halides of for­mula IB include, for example, poly(dimethylbutenyl ammo­nium chloride) - ⁇ , ⁇ -bis triethanolammonium chloride (as named by the manufacturer) sold under the trade names ONYXSPERSE® 12S and ONAMER® M by the Onyx Chemical Company, Jersey City, New Jersey, now owned by The Stepan Company, Northfield, Illinois.
  • ONYXSPERSE® and ONAMER® are aqueous solutions of the salt each containing, respec­tively, 28.5% and 29.5% actives and 12% and 1% sodium chloride respectively.
  • nonionic surfactants of formulas IIA, IIB and IIC and the nonionic alkyl polyglycoside surfactants used in the practice of the present invention are well known in commerce.
  • examples of the polyethylene glycol long chain alkyl ethers of formula IIA are sold under the Union Carbide (Danbury, Connecticut) trade name TERGITOL® or the Shell Chemical Company (Houston, Texas) trade name NEODOL® and are identified by the CTFA adopted name, pareth.
  • Suitable members of the group for the practice of the present invention are pareth-15-5, pareth-15-7, pareth-15-9, pareth-15-12, pareth-23-7, pareth-25-5, pareth-25-7, pareth-25-9, pareth-25-12, pareth-45-7, pareth-45-11 and pareth-45-13, where the first given numbers 15, 23, 25 and 45 indicate R4 alkyl chain lengths from 11 to 15, 12 to 13, 12 to 15 and 14 to 15 carbon atoms, respectively, and the second given numbers 5, 7, 9, 11, 12 and 13 indicate the average number (c) of ethyleneoxy groups.
  • polyethylene glycol alkyl phenyl ethers of formula IIB are available, for example, under the Rohm and Haas (Philadelphia, Pennsylvania) trade names TRITON® X and TRITON® N or the GAF Corporation (Wayne, New Jersey) trade names IGEPAL® CA and IGEPAL® CO and are identified by the CTFA adopted names of octoxynols and nonoxynols.
  • octoxynol-7 octoxynol-10 and octoxynol-13
  • R5 in formula IIB is C8 alkyl and d has an average value of 7, 10 and 13, respectively
  • R5 in formula IIB is C9 alkyl, and d has an average value of 7, 8, 9 and 13, respectively.
  • alkylamine oxides of formula IIC are sold under the trade name AMMONYX® by the Onyx Chemical Com­pany (Jersey City, New Jersey) and include, for example, lauramine oxide, myristylamine oxide, palmitamine oxide and stearamine oxide which are the CTFA adopted names for the compounds of formula IIC and R1 in each in­stance is methyl and the alkyl group has 12, 14, 16 and 18 carbon atoms respectively.
  • nonionic alkyl polyglycoside surfactants are sold by Staley Industrial Products of the A. E. Staley Manufacturing Company (Decatur, Illinois) and include, for example, APG-23-3 which is a surfactant of the alkyl polyglycoside class having an alkyl chain derived from a C12-C13 straight chain alcohol and an average of 3 glucose units in the polyglycoside moiety.
  • compositions of the invention contain from about 5.5 to about 20 weight percent of the polymeric quat­ernary ammonium salt of formulas IA and IB and from about 5 to about 50 weight percent of the nonionic surfactant, all amounts being based on total weight of the composi­tion.
  • Preferred ranges are from about 5 to about 10 weight percent of the polymeric quaternary salt and from about 5 to about 17 weight percent of the nonionic surfactant, and particularly preferred amounts are about 5.5 to about 6.5 weight percent of the polymeric quaternary salt and from about 7 to about 12 weight percent of the nonionic surfactant.
  • compositions may, in order to provide addi­tional benefits, optionally contain nonessential ingred­ients such as fragrances, dyes, pH adjusters such as triethylamine, brighteners, solvents such as eth­anol, and thickners.
  • nonessential ingred­ients such as fragrances, dyes, pH adjusters such as triethylamine, brighteners, solvents such as eth­anol, and thickners.
  • fragrances may be used in amounts up to about 0.7 weight percent
  • dyes in amounts up to about 0.02 weight percent
  • pH adjusters in amounts up to about 4 weight percent
  • brighteners in amounts up to about 0.5 weight percent
  • ethanol in amounts up to about 7 weight percent
  • thickners in amounts up to about 2.0 weight percent.
  • compositions are prepared by addition to water, with stirring and heating as necessary, of the nonionic surfactants(s), followed by alcohol if desired, followed by the polymeric quaternary ammonium salt, followed by the dyes, fragrances, brightners, pH adjusters or thickeners, stirring being continued at each stage to effect complete solution or homogeneous dispersion.
  • compositions of the invention possess very good detergency and bactericidal properties and further­more have very low eye and skin irritancy. They are therefore particularly valuable in household sanitizing and cleaning operations where such properties are desir­able, such as in laundry detergents and hard surface cleaners.
  • a number of formulations, composed as indicated in Table 1, each containing a quaternary ammonium salt and at least one nonionic surfactant were prepared using the procedure described above.
  • Formulations A-K each containing a polymeric quaternary of formulas IA or IB and one or more nonionic surfactants of formulas IIA, IIB or IIC or an alkyl poly­glycoside, are formulated in accordance with the inven­tion as described above and are within the ambit of the invention, whereas formulations L-O, each containing a monomeric quaternary halide, i.e. CYNCAL® 80, and a nonionic surfactant, were prepared for comparative pur­poses and are outside the scope of the invention.
  • Skin irritation scores are expressed in terms of Primary Irritation Index (P.I.I.) also in accordance with the standard FIFRA method. The lower the score thus obtained, the less irritating is the formulation.
  • P.I.I. Primary Irritation Index
  • formulations A, C and D prepared in accordance with the invention are markedly superior in detergency properties, as determined in both EMPA and Krefeld detergency test, to any of comparative formulations L, M and N.
  • Formulations A, B and C are also shown to be equally or more effective in antimicro­bial activity to comparative formulations L, M, N and O, and Formulation A is shown to have lower eye and skin irritancy than comparative formulation N.
  • the liquid laundry detergent formulations of the invention are formulated as concentrates. In use the concentrate is added to the wash water in such amounts as to provide good cleaning and sanitization. It has been found that about 1/2 cup (about 4 ounces) of concen­trate per wash load (or about 4 ounces per 16 gallons), which provides a use dilution of around 1:500, is ade­quate to achieve such purposes.

Landscapes

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

Abstract

Stable, isotropic liquid laundry detergent and sanitizer compositions comprising a polymeric linear quaternary ammonium salt, one or more nonionic surfactants and water.

Description

  • This invention relates to isotropic liquid laundry detergents containing polymeric quaternary ammonium salts in combination with one or more nonionic surfactants.
  • INFORMATION DISCLOSURE STATEMENT
  • U.S. Patent 3,771,989 discloses poly­meric polyelectrolytes, useful as algicides, having the formula:
    Figure imgb0001
    where n is an integer from 4 to 40, with molecular weights ranging from 1,000 to 10,000, which are chemically desig­nated poly[oxyethylene(dimethyliminio)ethylene(dimethyl­iminio)ethylene dichloride]. As far as is presently known, compounds of this class are not known to have useful bactericidal properties nor are they known to be useful for incorporation in laundry detergents.
  • U.S. Patents 3,931,319; 4,001, 432 and 4,012,446 disclose so-called "capped" polymers useful as "microbiocidal" agents, which have linear polymeric quaternary chains terminated by quaternary ammonium moieties, having the formula:
    Figure imgb0002
    where X⁻ is halide and "n is an integer from about 2 to about 30; where R′ and R˝ may be either (1) a primary or secondary alkyl radical having from 1 to 20 carbon atoms, (2) hydroxy or dihydroxy derivatives of R′ and R˝, (3) benzyl, or (4) benzyl containing at least one alkyl group...; where Z consists of from one to three aliphatic divalent radicals, each of which has 2 to 10 carbon atoms, each aliphatic radical containing 0 to 2 double bonds and 0 to 2 hydroxy substituents" and where "RIII, RIV and RV may be either (1) primary or secondary alkyl containing from 1 to 20 carbon atoms, or (2) hydroxy­ethyl ....",
  • U.S. Patent 4,027,020 discloses so-­called "randomly terminated" capped linear quaternary ammonium polymers generally similar to those described in U.S. Patents 3,931,319; 4,001,432 and 4,012,446 above prepared by reaction of a 1,4-dihalo-2-butene, XCH₂CH=­CHCH₂X, where X is halogen, with a mixture of a difunc­tional tertiary amine:
    Figure imgb0003
    and a monofunctional tertiary amine:
    Figure imgb0004
    The compounds are said to be effective against bacteria and algae and to a lesser extend against fungi. They are also stated to be non-foaming, a property which is said to be important in anti-microbial agents used in products and processes where the generation of foam is undesirable.
  • U.S. Patent 4,091,113 discloses "ran­domly terminated" capped linear quaternary ammonium poly­mers prepared in the same manner as described in U.S. Patent 4,027,020 supra. The quaternaries are said to be "uniquely excellent hair conditioning agents" which are "compatible in binary or tertiary systems with most of the lathering and cleansing surfactants used in hair conditioning consumer products". The patentee states that 40% aqueous solutions are non-irritating to the skin and that 4% aqueous solutions are non-irritating to the eyes. More specifically, the quaternaries are described as being compatible with surfactants and emulsi­fiers of the cationic, nonionic, amine oxide, alkylol­amide, amphoteric, aminoacetic or β-aminopropionic acid and betaine or betaine salt classes. The compositions are exemplified in Examples 28, 29 and 30 by formulations containing the polymeric quaternary which is produced by reaction of 1,4-bis-dimethylamino-2-butene, triethan­olamine and 1,4-dichloro-2-butene in water in combination with surfactants of the cationic (AMMONYX®4, i.e. stearal­konium chloride -Example 30), nonionic (TERGITOL® 15-S-12, i.e. pareth-15-12 - Example 29), alkylolamide (ONYXOL® 42, i.e. stearyl diethanolamide - Example 30 and SUPER AMIDE® GR, i.e. cocoyldiethanolamide - Example 28), ampho­teric (MIRANOL® C-2M-SF, i.e. cocoamphocarboxypropionate and SANDOPAN® TFL, i.e. oleoamphopropylsulfonate - both Example 28) and anionic (MAPROFIX® 60S, i.e. sodium laureth sulfate - Example 28) classes. As far as is presently known the compounds of the structural type disclosed in U.S. Patents 3,931,319; 4,001,432; 4,012,446; 4,027,020 and 4,091,113 above are not known to have been previously incorporated in laundry detergents.
  • U.S. Patent 4,333,862 discloses, as one possible cationic surfactant in liquid detergent compositions containing an anionic, a cationic and a nonionic surfactant, polyammonium salts of the formula:
    Figure imgb0005
    where R₃ is C₈-C₂₀ alkyl, alkenyl or aralkyl; each R₄ is C₁-C₄ alkyl or hydroxyalkyl; n is from 1 to 6; and m is from 1 to 3.
  • As noted above, polymeric linear quaternary ammonium salts of the structural types represented by those dis­closed in U.S. Patents 3,771,989; 3,931,319; 4,001,432; 4,012,446; 4,027,020 and 4,091,113 are not known to have been incorporated in laundry detergents. We have dis­covered that polymeric quaternary ammonium salts of those classes, when formulated in an aqueous medium with one or more nonionic surfactants, provide stable, isotropic liquid laundry detergents and sanitizer compositions having good detergency and bactericidal properties, which, in addition, are moderately irritating to the eyes and practically non-irritating to the skin.
  • Accordingly, the invention resides in stable, isotropic liquid laundry detergent and sanitizer composi­tions comprising: (A) a polymeric linear quaternary ammo­nium salt selected from the group consisting of a poly[oxy­ethylene)di-lower-alkyliminio)ethylene(di-lower-alkyliminio)-­ethylene dihalide] and a polymeric quaternary ammonium halide corresponding to formula IB hereinbelow; (B) one or more nonionic surfactants selected from the group consisting of the polyethylene glycol long chain alkyl ether, polyethylene glycol alkylphenyl ether, N-alkyl-­N,N-di-lower-alkylamine-N-oxide and alkyl polyglycoside classes; and (C) water.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • More specifically the isotropic liquid laundry detergent and sanitizer compositions of the invention comprise: (A) a polymeric linear quaternary ammonium salt selected from the group consisting of a poly[oxy­ethylene)di-lower-alkyliminio)ethylene(di-lower-alkyl­iminio)ethylene dihalide] having the formula:
    Figure imgb0006
    where R₁ is lower-alkyl having from one to four carbon atoms, a is an integer from 4 to 40, with an average value of 19, and X⁻ is halide, and a polymeric quaternary ammonium halide having the formula:
    Figure imgb0007
    where R₂ is hydroxy-lower-alkyl having from two to four carbon atoms, b is an integer from 27 to 57 and R₁ and X⁻ have the meanings given above; (B) one or more nonionic surfactants selected from the group consisting of a polyethylene glycol long chain alkyl ether having the formula:
    R₄
    Figure imgb0008
    OCH₂CH₂)cOH      IIA
    where R₄ is C₁₁-C₁₅ alkyl and c is an integer from 5 to 15, a polyethylene glycol alkylphenyl ether having the formula:
    Figure imgb0009
    where R₅ is C₈-C₉ alkyl and d is an integer from 7 to 13; an N-alkyl-N,N-di-lower-alkylamine-N-oxide having the formula:
    Figure imgb0010
    where R₁ has the meaning given above and an alkyl poly­glycoside; and (C) water.
  • The polymeric quaternary ammonium salts of for­mulas IA and IB used to prepare the compositions of the invention are well known classes of compounds. The poly­[oxyethylene)di-lower-alkyliminio)ethylene(di-lower-alkyl­iminio)ethylene dihalide] quaternaries of formula IA include, for example, poly[oxyethylene(dimethyliminio)­ethylene(dimethyliminio)ethylene dichloride] sold under the trade name BUSAN® 77 by Buckman Laboratories, Memphis, Tennessee as a 60% actives solution in water which is identified as WSCP (water soluble cationic polymer).
  • The polymeric quaternary ammonium halides of for­mula IB include, for example, poly(dimethylbutenyl ammo­nium chloride) -α,ω-bis triethanolammonium chloride (as named by the manufacturer) sold under the trade names ONYXSPERSE® 12S and ONAMER® M by the Onyx Chemical Company, Jersey City, New Jersey, now owned by The Stepan Company, Northfield, Illinois. ONYXSPERSE® and ONAMER® are aqueous solutions of the salt each containing, respec­tively, 28.5% and 29.5% actives and 12% and 1% sodium chloride respectively.
  • The nonionic surfactants of formulas IIA, IIB and IIC and the nonionic alkyl polyglycoside surfactants used in the practice of the present invention are well known in commerce. Examples of the polyethylene glycol long chain alkyl ethers of formula IIA are sold under the Union Carbide (Danbury, Connecticut) trade name TERGITOL® or the Shell Chemical Company (Houston, Texas) trade name NEODOL® and are identified by the CTFA adopted name, pareth. Suitable members of the group for the practice of the present invention are pareth-15-5, pareth-15-7, pareth-15-9, pareth-15-12, pareth-23-7, pareth-25-5, pareth-25-7, pareth-25-9, pareth-25-12, pareth-45-7, pareth-45-11 and pareth-45-13, where the first given numbers 15, 23, 25 and 45 indicate R₄ alkyl chain lengths from 11 to 15, 12 to 13, 12 to 15 and 14 to 15 carbon atoms, respectively, and the second given numbers 5, 7, 9, 11, 12 and 13 indicate the average number (c) of ethyleneoxy groups.
  • The polyethylene glycol alkyl phenyl ethers of formula IIB are available, for example, under the Rohm and Haas (Philadelphia, Pennsylvania) trade names TRITON® X and TRITON® N or the GAF Corporation (Wayne, New Jersey) trade names IGEPAL® CA and IGEPAL® CO and are identified by the CTFA adopted names of octoxynols and nonoxynols. These include, for example, octoxynol-7, octoxynol-10 and octoxynol-13, where R₅ in formula IIB is C₈ alkyl and d has an average value of 7, 10 and 13, respectively, and nonoxynol-7, nonoxynol-8, nonoxynol-9 and nonoxynol-­13, etc. where R₅ in formula IIB is C₉ alkyl, and d has an average value of 7, 8, 9 and 13, respectively.
  • The alkylamine oxides of formula IIC are sold under the trade name AMMONYX® by the Onyx Chemical Com­pany (Jersey City, New Jersey) and include, for example, lauramine oxide, myristylamine oxide, palmitamine oxide and stearamine oxide which are the CTFA adopted names for the compounds of formula IIC and R₁ in each in­stance is methyl and the alkyl group has 12, 14, 16 and 18 carbon atoms respectively.
  • The nonionic alkyl polyglycoside surfactants are sold by Staley Industrial Products of the A. E. Staley Manufacturing Company (Decatur, Illinois) and include, for example, APG-23-3 which is a surfactant of the alkyl polyglycoside class having an alkyl chain derived from a C₁₂-C₁₃ straight chain alcohol and an average of 3 glucose units in the polyglycoside moiety.
  • Although it is preferred in the practice of the present invention to include either one or the other of the polymeric quaternary ammonium salts represented by formulas IA and IB, it is also contemplated that mix­tures of salts of those two structural types can, if desired, be used in the liquid laundry detergent formula­tions of the invention.
  • The compositions of the invention contain from about 5.5 to about 20 weight percent of the polymeric quat­ernary ammonium salt of formulas IA and IB and from about 5 to about 50 weight percent of the nonionic surfactant, all amounts being based on total weight of the composi­tion. Preferred ranges are from about 5 to about 10 weight percent of the polymeric quaternary salt and from about 5 to about 17 weight percent of the nonionic surfactant, and particularly preferred amounts are about 5.5 to about 6.5 weight percent of the polymeric quaternary salt and from about 7 to about 12 weight percent of the nonionic surfactant.
  • The compositions may, in order to provide addi­tional benefits, optionally contain nonessential ingred­ients such as fragrances, dyes, pH adjusters such as triethylamine, brighteners, solvents such as eth­anol, and thickners. Generally fragrances may be used in amounts up to about 0.7 weight percent, dyes in amounts up to about 0.02 weight percent, pH adjusters in amounts up to about 4 weight percent, brighteners in amounts up to about 0.5 weight percent, ethanol in amounts up to about 7 weight percent, and thickners in amounts up to about 2.0 weight percent.
  • The compositions are prepared by addition to water, with stirring and heating as necessary, of the nonionic surfactants(s), followed by alcohol if desired, followed by the polymeric quaternary ammonium salt, followed by the dyes, fragrances, brightners, pH adjusters or thickeners, stirring being continued at each stage to effect complete solution or homogeneous dispersion.
  • The compositions of the invention possess very good detergency and bactericidal properties and further­more have very low eye and skin irritancy. They are therefore particularly valuable in household sanitizing and cleaning operations where such properties are desir­able, such as in laundry detergents and hard surface cleaners.
  • The manner and process of making and using the invention, and the best mode contemplated by the inven­tors for carrying out the invention, will now be described so as to enable any person skilled in the art to which it pertains to make and to use the same.
  • EXAMPLES
  • A number of formulations, composed as indicated in Table 1, each containing a quaternary ammonium salt and at least one nonionic surfactant were prepared using the procedure described above.
  • Formulations A-K, each containing a polymeric quaternary of formulas IA or IB and one or more nonionic surfactants of formulas IIA, IIB or IIC or an alkyl poly­glycoside, are formulated in accordance with the inven­tion as described above and are within the ambit of the invention, whereas formulations L-O, each containing a monomeric quaternary halide, i.e. CYNCAL® 80, and a nonionic surfactant, were prepared for comparative pur­poses and are outside the scope of the invention. Table 1
    Formulation (Amts. in weight % of actives)
    Ingredient A B C D E F G H I J K L M N O
    ONAMER® M (29.5) 6.4 - - - - 6 - - - - - - - - -
    ONYXSPERSE® 12S (28.5%) - 5.5 - - 6 - 6 6 6 5.5 5.5 - - - -
    BUSAN® 77 (60%) - - 6.4 6.4 - - - - - - - - - - -
    CYNCAL® 80 (80%) - - - - - - - - - - - 6.4 6.4 6.4 5.5
    pareth-23-7 - - 12 - 5 - - - - - - 17 12 - -
    pareth-45-7 12 - - 12 - 12 - - - - - - - 12 -
    TERGITOL-24-L-98 NMW - 10 - - - - - 9 - - - - - - 10
    pareth-15-12 - - - - - - 9 - 5 - - - - - -
    pareth-15-9 - - - - - - - - - 5 8.3 - - - -
    nonoxynol-9 - - - - - - - - - 2.6 - - - - -
    AMMONYX® LO - - - - 2 - - - - - 3 - - - -
    APG 23-3 (46%) - - - - - - - - 7 2.6 - - - - -
    EtOH - - - - 7 - - 5 - - - - - - -
    Dye, fragrance, water q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s. q.s.
  • The formulations of the invention and the compar­ative formulations were tested for cleaning efficacy using the standard EMPA and Krefeld detergency tests; for germicidal activity against K. pneumoniae ATCC 4352 and S. aureus ATCC 6538 using the EPA-approved Petrocci-­Clark test procedure [Proposed Test Method for Antimicro­bial Laundry Additives, Petrocci and Clark, J. Ass. Offic. Anal. Chem. 52(4), 836-842 (1969)] which is a simu­lated in-use test method (see EPA Publication DIS/TSS-­13, May 2, 1979); for eye irritation in rabbits using the standard FIFRA method (described at 40 C.F.R. 163.81-­4); and for skin irritation using the standard FIFRA dermal irritation test in rabbits (NAS 1138 modification described at 40 C.F.R. 163.81-5).
  • The EMPA and Krefeld detergency tests used in the present study are described in U.S. Patent 4,576,729 except that the temperature of the wash and rinse water was 105°F instead of 120°-130°F. In the EMPA test (a test by the Swiss Federal Testing Station in Switzerland), the standard soil is an India ink and olive oil emollient (an oily type soil), and in the Krefeld test (a test by the Wascherei Foschungs Institute of Krefeld, West Germany), the soil is 84% clay, 8% lamp black, 4% black iron oxide and 2% yellow iron oxide oversprayed with a solution of 3.4% lanolin dissolved in carbon tetra­chloride and salt solution (the salt to resemble human perspiration). The cleaning efficacy, expressed as % Soil Removal, was calculated in each test procedure for the test swatches as follows, the values obtained for any given detergent formulation being the average of the individual values so determined:
    Figure imgb0011
    where:
    Rw = Average reflectance of washed soiled cloths
    Rs = Average reflectance of unwashed soiled cloths
    Ro = Average reflectance of unsoiled cloths before washing
    Thus the higher the value for % Soil Removal, the greater the detergency.
  • In the germicidal activity test, EPA protocols require a germ reduction of at least 99.90% for laundry sanitizers against the two test organisms, K. pneumoniae and S. aureus.
  • Eye irritation results are expressed in terms of Draize scores in accordance with the standard FIFRA method.
  • Skin irritation scores are expressed in terms of Primary Irritation Index (P.I.I.) also in accordance with the standard FIFRA method. The lower the score thus obtained, the less irritating is the formulation.
  • The results obtained are set forth in Tables 2, 3 and 4 where EMPA and Krefeld detergency results are expressed in terms of soil removal values; the antimicro­bial activity is expressed in terms of percent germ reduc­tion and antimicrobial effectiveness based on the above-­noted EPA protocols; eye irritation is expressed in terms of Draize scores; and skin irritation is expressed as P.I.I. values. Table 2
    (EMPA/Krefelt Detergency)
    Formulation EMPA Krefeld
    A 35 43
    C 36.4 40.6
    D 36 40
    L 27.0 9.2
    M 22.8 7.9
    N 26 10
    Table 3
    (Antimicrobial Activity vs. K. pneumoniae and S. aureus)
    Formulation % Germ Reduction Sanitization Result
    A 99.9 Effective
    B 99.9 Effective
    C 99.9 Effective
    L 99.9 Effective
    M 99.9 Effective
    N 99.9 Effective
    O 99.7 Not Effective
    Table 4
    (Irritancy Scores)
    Formulation Eye Irritancy (Highest mean Draize Score) Skin Irritancy (P.I.I.)
    A 16.3 (unwashed) 0.71
    7.7 (washed)
    N 73 (unwashed) 2.78
    58 (washed)
  • These results show that formulations A, C and D prepared in accordance with the invention are markedly superior in detergency properties, as determined in both EMPA and Krefeld detergency test, to any of comparative formulations L, M and N. Formulations A, B and C are also shown to be equally or more effective in antimicro­bial activity to comparative formulations L, M, N and O, and Formulation A is shown to have lower eye and skin irritancy than comparative formulation N.
  • The liquid laundry detergent formulations of the invention are formulated as concentrates. In use the concentrate is added to the wash water in such amounts as to provide good cleaning and sanitization. It has been found that about 1/2 cup (about 4 ounces) of concen­trate per wash load (or about 4 ounces per 16 gallons), which provides a use dilution of around 1:500, is ade­quate to achieve such purposes.

Claims (10)

1. A liquid laundry detergent and sanitizing composition comprising: (A) a polymeric linear quaternary ammonium salt which is a compound having the formula:
Figure imgb0012
where R₁ is lower-alkyl having from one to four carbon atoms, a is an integer from 4 to 40 and X⁻ is halide, or a compound having the formula:
Figure imgb0013
where R₂ is hydroxy-lower-alkyl having from two to four carbon atoms, b is an integer from 27 to 57 and R₁ and X⁻ have the meanings given above; (B) one or more compound nonionic surfactants, said nonionic surfactants being a compound having the formula:
R₄(OCH₂CH₂)cOH      IIA
where R₄ is C₁₁-C₁₅ alkyl and c is an integer from 5 to 15, a compound having the formula:
Figure imgb0014
where R₅ is C₈-C₉ alkyl and d is an integer from 7 to 13, or a compound having the formula:
Figure imgb0015
where R₁ has the meaning given above, and an alkyl polyglycoside; and (C) water.
2. A composition according to claim 1, wherein the quaternary ammonium salt is a compound of formula IA.
3. A composition according to claim 1, wherein the quaternary ammonium salt is a compound of formula IB.
4. A composition according to any one of the preceding claims, containing from about 5.5 to about 20 weight percent of the quaternary ammonium salt and from about 5 to about 50 weight percent of the nonionic surfactant.
5. A composition according to claim 4, which contains from about 5.5 to about 10 weight percent of the quaternary ammonium salt and from about 5 to about 17 weight percent of the nonionic surfactant.
6. A composition according to any one of the preceding claims, which contains a nonionic surfactant of formula IIA.
7. A composition according to any one of the preceding claims, which contains a mixture of nonionic surfactants of formulas IIA and IIC.
8. A composition according to claim 1, containing about 6 weight percent of poly[oxyethylene(dimethylimino)ethylene (dimethyliminio)ethylene dichloride] and about 12 weight percent of pareth-45-7.
9. A composition according to claim 1, containing about 6 weight percent of poly(dimethyl butenyl ammonium chloride)-­α,ω-bis-triethanolammonium chloride and about 12 weight percent of pareth-45-7.
10. A composition according to claim 6 or 9, which includes up to about 7 weight percent of ethanol.
EP19880106946 1986-11-26 1988-04-29 Isotropic laundry detergents Withdrawn EP0339120A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US06/935,658 US4755327A (en) 1986-11-26 1986-11-26 Isotropic laundry detergents containing polymeric quaternary ammonium salts
EP19880106946 EP0339120A1 (en) 1988-04-29 1988-04-29 Isotropic laundry detergents

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP19880106946 EP0339120A1 (en) 1988-04-29 1988-04-29 Isotropic laundry detergents

Publications (1)

Publication Number Publication Date
EP0339120A1 true EP0339120A1 (en) 1989-11-02

Family

ID=8198931

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19880106946 Withdrawn EP0339120A1 (en) 1986-11-26 1988-04-29 Isotropic laundry detergents

Country Status (1)

Country Link
EP (1) EP0339120A1 (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3771989A (en) * 1971-11-26 1973-11-13 Buckman Labor Inc Method of controlling the growth of algae
FR2271840A1 (en) * 1974-05-21 1975-12-19 Procter & Gamble
FR2345997A1 (en) * 1976-03-29 1977-10-28 Kao Corp TRANSPARENT COMPOSITION FOR RINSING THE HAIR
US4091113A (en) * 1975-09-04 1978-05-23 Kewanee Industries, Inc. Randomly terminated capped polymers
EP0000224A1 (en) * 1977-06-29 1979-01-10 THE PROCTER & GAMBLE COMPANY Liquid detergent composition for improved greasy soil removal
EP0076136A2 (en) * 1981-09-28 1983-04-06 Alcon Laboratories, Inc. Ophthalmic solutions
EP0133900A2 (en) * 1983-08-10 1985-03-13 Sterling Drug Inc. Liquid disinfectant laundry detergents

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3771989A (en) * 1971-11-26 1973-11-13 Buckman Labor Inc Method of controlling the growth of algae
FR2271840A1 (en) * 1974-05-21 1975-12-19 Procter & Gamble
US4091113A (en) * 1975-09-04 1978-05-23 Kewanee Industries, Inc. Randomly terminated capped polymers
FR2345997A1 (en) * 1976-03-29 1977-10-28 Kao Corp TRANSPARENT COMPOSITION FOR RINSING THE HAIR
EP0000224A1 (en) * 1977-06-29 1979-01-10 THE PROCTER & GAMBLE COMPANY Liquid detergent composition for improved greasy soil removal
EP0076136A2 (en) * 1981-09-28 1983-04-06 Alcon Laboratories, Inc. Ophthalmic solutions
EP0133900A2 (en) * 1983-08-10 1985-03-13 Sterling Drug Inc. Liquid disinfectant laundry detergents

Similar Documents

Publication Publication Date Title
CA2281753C (en) Ultramild antibacterial cleaning composition for frequent use
JP5615708B2 (en) Formulation containing antimicrobial composition
US4597975A (en) Iodine surface active compositions
US3849348A (en) Detergent compositions
EP0214868B1 (en) Surfactants for use in cleaning compositions
CA1131096A (en) Detergent compositions
AU614317B2 (en) Stable, liquid laundry detergents
US4456543A (en) Bisbiguanide based antibacterial cleansing products
NO802408L (en) SOLUTION COMPOUNDS.
JPS59161496A (en) Detergent composition
US6339057B1 (en) High foaming detergent composition having a non-ionic surfactant base
US4755327A (en) Isotropic laundry detergents containing polymeric quaternary ammonium salts
WO1999019438A1 (en) High foaming detergent composition having non-ionic surfactant base
AU680536B2 (en) Disinfectant-detergent composition
JPH0393711A (en) Shampoo composition
JPH08512145A (en) Contact lens cleaning solution containing quaternary ammonium substituted phosphate ester
US4091113A (en) Randomly terminated capped polymers
JPH0633405B2 (en) Cleaning composition
AU604275B2 (en) Isotropic laundry detergents containing polymeric quaternary ammonium salts
CA2014991A1 (en) Fabric softener composition
IE52291B1 (en) Amphoteric fatty acid,amino acid salts and their use in detergent compounds and compositions
JP2003040719A (en) Antibacterial agent
EP0339120A1 (en) Isotropic laundry detergents
JP3082386B2 (en) Shampoo composition
AU748069B2 (en) High foaming detergent composition having a non-ionic surfactant base

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE ES FR GB GR IT LI NL SE

17P Request for examination filed

Effective date: 19900427

17Q First examination report despatched

Effective date: 19920609

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19921228