CA1226407A - Aqueous fabric softening composition - Google Patents

Aqueous fabric softening composition

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Publication number
CA1226407A
CA1226407A CA000479169A CA479169A CA1226407A CA 1226407 A CA1226407 A CA 1226407A CA 000479169 A CA000479169 A CA 000479169A CA 479169 A CA479169 A CA 479169A CA 1226407 A CA1226407 A CA 1226407A
Authority
CA
Canada
Prior art keywords
weight
fabric softening
softening composition
water
softener
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.)
Expired
Application number
CA000479169A
Other languages
French (fr)
Inventor
Robert M. Butterworth
John R. Martin
Edwin Willis
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.)
Unilever PLC
Original Assignee
Unilever PLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever PLC filed Critical Unilever PLC
Application granted granted Critical
Publication of CA1226407A publication Critical patent/CA1226407A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/046Salts
    • 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
    • C11D1/38Cationic compounds
    • C11D1/645Mixtures of compounds all of which are cationic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • 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
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/523Carboxylic alkylolamides, or dialkylolamides, or hydroxycarboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain one hydroxy group per alkyl group
    • 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
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/526Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 are polyalkoxylated
    • 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
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

A B S T R A C T

An aqueous fabric softening composition containing less than 10% cationic softener also includes an alkoxylated fatty acid amide containing less than 5 alkylene oxide groups per molecule, such as tallow ethanolamide or diethanolamide in an amount such as 110%, together with an ionic salt of Li+, Ca++, Mg++ or Al+++.
The compositions exhibit low viscosities which are stable on storage.

Description

1226~07 - 1 - C.3031 AQUEOUS FABRIC SOFTENING COMPOSITION

This invention relates to an aqueous fabric softening composition, in particular to a composition containing a water-insoluble cat ionic fabric softener.

British Patent Specification No GAB 1 104 441 (UNILEVER/TUNE) discloses aqueous fabric softening compositions which contain up to 10~ by weight of a water-insoluble cat ionic fabric softener together with a fatty acid ethanolamide which is included to enhance the softening effect and to provide an anti-static finish on fabrics treated therewith. Sodium carbonate may be added to these compositions to control product thickness.

As the cat ionic softener is water-insoluble, this can lead to high product viscosities, especially on storage.
We have now surprisingly discovered that products with lower viscosities, which are more stable on storage, can be obtained if the product contains specific electrolytes.

lZZ64()7
- 2 - C.3031 Thus, according to the invention there it provided an aqueous fabric softening composition comprising:

( i) an aqueous base;

( ii) at least 1% to less than 10% by weight of a water-insoluble cat ionic fabric softener;

(iii) at least I of a non ionic material which comprises an alkaline oxide adduce of a fatty acid aside, the fatty acid aside containing at least 10 carbon atoms and the adduce containing an average of less than 5 alkaline oxide groups per molecule, the total level of the cat ionic softener and the non ionic material being not more than 36% by weight, preferably not more than about 25% by weight; and ( iv) an electrolyte selected from ionic salts of lithium, magnesium, calcium, aluminum and mixtures thereof.

The level of cat ionic softener in the composition is preferably more than 6% to less than 10% by weight, most preferably from about 7% to about 9% by weight. The level of the non ionic material in the composition is preferably less than 10% by weight, most preferably from about 2% to about 8% by weight. The total level of the cat ionic softener and the non ionic material is preferably at least 12% by weight. The weight ratio of the cat ionic softener to the non ionic material is preferably at least 1:1, such as between about 1.5:1 and about 5:1.

The water-insoluble cat ionic fabric softener can be any fabric-substantive cat ionic compound which has a volubility in water at pi 2.5 and 20C of less than 10 g/l. Highly preferred materials are qua ternary ammonium ~2264()7
- 3 - C.3031 salts having two C12-C24 alkyd or alkenyl chains, optionally substituted or interrupted by functional groups such as -OH, -O-, -CON, -COO-, etc.

Well known species of substantially water-insoluble qua ternary ammonium compounds have the formula \ N / X

wherein Al and R2 represent hydrocarbyl groups from about 15 12 to about 24 carbon atoms; R3 and R4 represent hydrocarbyl groups containing from 1 to about 4 carbon atoms; and X is an anion, preferably selected from halide, methyl sulfate and ethyl sulfate radicals. Representative examples of these qua ternary softeners include disallow dim ethyl ammonium chloride; disallow dim ethyl ammonium methyl sulfate; dihexadeeyl dim ethyl ammonium chloride;
di(hydrogenated tallow alkyd) dim ethyl ammonium chloride;
dioetadeeyl dim ethyl ammonium chloride; dieicosyl dim ethyl ammonium chloride; didoeosyl dim ethyl ammonium chloride;
di(hydrogenated tallow) dim ethyl ammonium methyl sulfate;
dihexadeeyl deathly ammonium chloride; di(coconut alkyd) dim ethyl ammonium chloride. Disallow dim ethyl ammonium chloride, di(hydrogenated tallow alkyd) dim ethyl ammonium chloride, decant alkyd) dim ethyl ammonium chloride and di(coconut alkyd) dim ethyl ammonium methosulfate are preferred.

~2~6407 Another class of preferred water-insoluble cat ionic materials are the alkylimidazolinium salts believed to have the formula:

SHEA - SHEA

N No C2H4 C R7 wherein R6 is an alkyd or hydroxyalkyl group containing from 1 to 4, preferably 1 or 2 carbon atoms, R7 is an alkyd or at-Kenya group containing from 8 to 25 carbon atoms, R8 is an alkyd or alkenyl group containing from 8 to 25 carbon atoms, and Rug is hydrogen or an alkyd containing from 1 to 4 carbon atoms and A is an anion, preferably a halide, methosulfate or ethosulfate. Preferred imidazolinium salts include 1-methyl-l-ttallowylamido-) ethyl -2-tallowyl- dodder imp idazolinium methosulfate and l-methyl-l-(palmitoylamido)ethyl -2-octadecyl-4,5- dihydroimidazolinium chloride. Other useful imidazolinium materials are 2-heptadecyl-1-methyl-1- (2-stearylamido)-ethyl-imidazolinium chloride and laurel-droxyethyl-l-oleyl-imidazolinium chloride.

Representative commercially available materials of the above classes are the qua ternary ammonium compounds Argued 2HT (ox AWAKES); Noramium MUSH (ox SEIKO); Aliquat-2HT
(Trade Mark of General Mills Inch and the imidazolinium Ye I
- 5 - C.3031 compounds Varisoft 475 (Trade Mark of Shrieks Company, Columbus Ohio) and Rocket Wow (Trade Mark of REDO).

The non ionic material is or includes an alkaline oxide adduce of a fatty acid aside but may also include other alkoxylated or non-alkoxylated non ionic materials.

Alkaline oxide adduces of fatty asides useful in the present invention, preferably have the general formula ( n on ox R I -N
(CnH2n) z wherein R10 is an alkyd or alkenyl group having at least 10 carbon atoms, most preferably from 10 to 22 carbon atoms, n is 2 or 3 and x and z in total are not more than
4.0, preferably from about 0.5 to about 3.5 while one of x and z can be zero. Examples of such materials include tallow monoethanolamide and diethanolamide, and the corresponding coconut and soya compounds.
The viscosity of the product, when measured at 110 sea 1 shear rate should be less than about 150 cup, preferably between about 20 and about 100 cup and the product can be added as such to a fabric rinse liquor or may be pre-diluted with water.

Preferably, the compositions of the invention contain substantially no anionic material, in particular no anionic surface active materials. If such materials are present, the weight ratio of the cat ionic material to :~226~7 - 6 - C.3031 the anionic material should preferably be more than 10:1, such as more than 100:1.

The compositions include specific electrolytes to assist in controlling the viscosity of the product. A
suitable electrolyte level in the compositions is from 0.01% to 0.5%, most preferably from about 0.02% to about 0.2%, measured as the an hydrous salt. Examples of suitable electrolytes include lithium chloride, calcium chloride, magnesium chloride and aluminum chloride.
mixtures of two or more of these electrolytes or mixtures thereof with sodium or potassium salts may also be used.

The compositions may include low levels of solvent for the cat ionic fabric softener. Indeed, the cat ionic raw materials will often include isopropanol as a solvent.
It is preferred that the level of isopropanol or any other Cluck mandrake alcohol in the composition is less than about 5% by weight, most preferably less than about 2.5%
by weight.

Additionally, the composition can contain substances for maintaining the stability of the product on cold storage. Examples of such substances include polyhydric alcohols such as ethylene glycol, propylene glycol, glycerol and polyethylene glycol. A suitable level for such materials is from about 0.5% to about 5%, preferably about 1.0% to 2.0% by weight.

The compositions of the invention may further include other additional ingredients including colorants, perfumes, preservations, anti-foams, optical brighteners, pacifiers, pi buffers (the preferred pi for the compositions is between about 3 and about 8, such as from about 4 to about 6), further viscosity modifiers, ~640~
- 7 - C.3031 non-cationic fabric conditioning agents, anti-shrinkage agents, anti-wrinkle agents, fabric crisping agents, spotting agents, soil-release agents, germicides, anti-oxidants and anti-corrosion agents.

The compositions of the invention may be prepared by a variety of methods. One suitable method is to form a molten mixture of the cat ionic fabric softener and the non ionic material, add this molten mixture to water with stirring to form a dispersion and thereafter adding the electrolyte (such as in the form of a concentrated solution thereof) and any optional ingredients.

The invention will now be illustrated by the following Examples, where all parts and percentages are by weight. Where commercially available materials are referred to, the percentages quoted are of the active ingredients therein. Viscosities were measured in a Hake Roto-viscometer (Model RV2) at 110 sea 1 at 25C.

Compositions were prepared according to the formulations in the following Tables. The compositions were prepared by forming a molten mixture of the cat ionic and non ionic ingredients at 65C, adding to water at the same temperature, stirring to form a dispersion, adding electrolyte in the form of a saturated solution, cooling and the adding perfume. The compositions were made in batches of 100g. The dispersion was formed by stirring for 7 minutes at 500 rum.

~226407 - 8 - C.3031 EXAMPLE NO: 1 2 3 4 5 6 7 In rodent (%) g Argued 2HT1 8.0 9.09.0 7.5 5.0 9.5 6.0 Tallow diethanolamide 2.0 - - - 5.0 Soya diethanolamide - - - 7.5 - 9.5 go Coconut diethanolamide - 6.0 Coconut monoethanolamide - - 6.0 Calcium chloride 0.02 0.05 0.05 0.03 0.01 0.05 0.02 Water and minor ingredients ----------------balance-----------------1 - A commercially available di-hardened tallow dim ethyl ammonium chloride (about 82% active - balance water and isopropanol) EXAMPLE NO: 8 PA 9 PA
Ingredients (%) Arrowhead 2HT 6.0 6.0 9.0 9.0 Tallow monoethanolamide 3.0* 3.0 Tallow diethanolamide3.0 3.0 Coconut diethanolamide - - 6.0 6.0 Calcium chloride 0.05 - 0.04 Sodium chloride - 0.05 - 0.04 Water and minor ingredients ---------balance------------Initial viscosity (cup) 72 123 93 163 * I of the tallow monoethanolamide can be replaced by I hardened tallow fatty acid.

i2;~6407 - 9 - C.3031 EXAMPLE NO* 10 11 12 Ingredient I) Argued 2HT 9.0 7.5 6.0
5 SDEA2 6.0 7.5 9.0 Calcium chloride 0.05 0.05 0.05 Water and minor ingredients -balance-------Initial viscosity (cup) 72 126 148 Note 2 - Soya diethanolamide (MacKamide S ox McIntyre Co).

In order to demonstrate the influence of the number of alkaline oxide groups in the non ionic adduce, the following compositions were prepared as described in Example 1 and their viscosities measured:
EXAMPLE NO: 13 14 AYE
Ingredient (%) Argued 2HT 9.0 9.0 9.0 25 Coconut monoethanolamide 6.0 Soya diethanolamide - 6.0 Genogen COO 503 - - 6.0 Calcium chloride 0.05 0.05 0.05 Water -------balance-------Initial viscosity (cup) 85 72 >500 ~226~g:)7 - 10 - C.3031 Note:

3 - A commercially available material ox HOECHST A
which is believed to be the addition product of coconut fatty monoethanolamide with 5 mows of ethylene oxide.

This experiment shows that an ethoxylated aside, where the number of ethylene oxide groups in the molecule is lower than 5, produces a product with an acceptably low initial viscosity, whereas the product (Example AYE) where the number of ethylene oxide groups is not below 5 has an unacceptably high initial viscosity.

Claims (6)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE PROPERTY OR
PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An aqueous fabric softening composition comprising:

( i) an aqueous base;

( ii) at least 1% to less than 10% by weight of a water-insoluble cationic fabric softener;

(iii) at least 1% of a nonionic material which comprises an alkylene oxide adduct of a fatty acid amide, the fatty acid amide containing at least 10 carbon atoms and the adduct containing an average of less than 5 alkylene oxide groups per molecule, the total level of the cationic softener and the nonionic material being not more than 36% by weight.

( iv) an electrolyte selected from ionic salts of lithium, magnesium, calcium, aluminium and mixtures thereof.
2. An aqueous fabric softening composition according to Claim 1, wherein the level of said water-insoluble cationic fabric softener is more than 6% by weight of the composition.
3. An aqueous fabric softening composition according to Claim 1, wherein the level of said nonionic material is less than 10% by weight of the composition.
4. An aqueous fabric softening composition according to Claim 1, wherein the weight ratio of said water-insoluble cat ionic fabric softener to said nonionic material is at least 1:1.
5. An aqueous fabric softening composition according to Claim 1, wherein the level of said electrolyte is from 0.01% to 0.5% by weight of the composition, measured as the anhydrous salt.
6. A process for preparing an aqueous fabric softening composition according to Claim 1, the process comprising the steps of adding a molten mixture of the cationic softener and the nonionic material to water with stirring to form a dispersion and thereafter adding the electrolyte.
CA000479169A 1984-04-19 1985-04-15 Aqueous fabric softening composition Expired CA1226407A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB848410319A GB8410319D0 (en) 1984-04-19 1984-04-19 Aqueous fabric softening composition
GB8410319 1984-04-19

Publications (1)

Publication Number Publication Date
CA1226407A true CA1226407A (en) 1987-09-08

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ID=10559919

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000479169A Expired CA1226407A (en) 1984-04-19 1985-04-15 Aqueous fabric softening composition

Country Status (7)

Country Link
EP (1) EP0159922A3 (en)
JP (1) JPS60231868A (en)
AU (1) AU560746B2 (en)
CA (1) CA1226407A (en)
ES (1) ES8706195A1 (en)
GB (1) GB8410319D0 (en)
ZA (1) ZA852865B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6339874B2 (en) * 2014-06-27 2018-06-06 花王株式会社 Method for producing emulsion composition

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1104441A (en) * 1964-07-08 1968-02-28 Unilever Ltd Fabric conditioner
US3974076A (en) * 1974-01-11 1976-08-10 The Procter & Gamble Company Fabric softener
DE2605502A1 (en) * 1976-02-12 1977-08-18 Exquisit Kosmetik Gmbh Washing and rinsing composition for softening textiles - nonionic surfactant, softening agent and polyglycol difatty acid ester
DE2930061A1 (en) * 1979-07-25 1981-02-19 Hoechst Ag SOFT SOFTENER
US4439335A (en) * 1981-11-17 1984-03-27 The Procter & Gamble Company Concentrated fabric softening compositions
JPS58186674A (en) * 1982-04-23 1983-10-31 三洋化成工業株式会社 Softening finish composition
JPS58186673A (en) * 1982-04-23 1983-10-31 三洋化成工業株式会社 Softener composition for fiber product

Also Published As

Publication number Publication date
ES8706195A1 (en) 1987-06-01
AU560746B2 (en) 1987-04-16
ZA852865B (en) 1986-12-30
GB8410319D0 (en) 1984-05-31
EP0159922A2 (en) 1985-10-30
EP0159922A3 (en) 1987-03-25
JPS60231868A (en) 1985-11-18
ES542352A0 (en) 1987-06-01
AU4125285A (en) 1985-10-24

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