AU3217297A - Clear, concentrated liquid fabric softener compositions - Google Patents

Clear, concentrated liquid fabric softener compositions

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Publication number
AU3217297A
AU3217297A AU32172/97A AU3217297A AU3217297A AU 3217297 A AU3217297 A AU 3217297A AU 32172/97 A AU32172/97 A AU 32172/97A AU 3217297 A AU3217297 A AU 3217297A AU 3217297 A AU3217297 A AU 3217297A
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Australia
Prior art keywords
composition
softener
fatty
ammonium surfactant
diamido
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AU32172/97A
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AU737508B2 (en
Inventor
Jean-Paul Grandmaire
Anita Hermosilla
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Colgate Palmolive Co
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Colgate Palmolive Co
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Priority claimed from AU45250/96A external-priority patent/AU691720B2/en
Priority claimed from US08/662,714 external-priority patent/US5656585A/en
Application filed by Colgate Palmolive Co filed Critical Colgate Palmolive Co
Publication of AU3217297A publication Critical patent/AU3217297A/en
Application granted granted Critical
Publication of AU737508B2 publication Critical patent/AU737508B2/en
Anticipated expiration legal-status Critical
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    • 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
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic compounds
    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0017Multi-phase liquid compositions
    • C11D17/0021Aqueous microemulsions
    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/43Solvents
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/005Compositions containing perfumes; Compositions containing deodorants
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/463Compounds containing quaternary nitrogen atoms derived from monoamines
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M23/00Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
    • D06M23/10Processes in which the treating agent is dissolved or dispersed in organic solvents; Processes for the recovery of organic solvents thereof
    • 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
    • C11D1/40Monoamines or polyamines; Salts thereof
    • 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
    • C11D1/528Carboxylic amides (R1-CO-NR2R3), where at least one of the chains R1, R2 or R3 is interrupted by a functional group, e.g. a -NH-, -NR-, -CO-, or -CON- 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
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Dispersion Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

Clear. Concentrated Liquid Fabric Softener Compositions
A. BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to rinse cycle fabric softener compositions. More particularly it relates to aqueous liquid microemulsion fabric softener compositions that are clear, i.e , transparent even when highly concentrated.
2. Description of Related Art
U.S 3,892,669 issued to A.A Rapisarda et al. relates to a clear aqueous fabric softening composition containing a solubilized tetra alkyl quaternary ammonium salt having two short-chain alkyl and two long-chain alkyl groups, about 5% to about 25% of the latter having methyl and ethyl branching on the 2-carbon atom. Solubilization is effected by the presence of solubilizers comprising aryl sulfonates, diols, ethers, low molecular weight quaternaries, sulfobetaines, tauπnes, sulfoxides and non-ionic surfactants U.S 4,149,978 issued to P C.E Goffinet describes textile treatment compositions comprising a water-soluble fabric softener and a C12 - C40 hydrocarbon optionally together with a water-soluble cationic surfactant. The preferred fabric softeners are quaternary ammonium salts having two C10 - C22 alkyl chains U.S 4,351 ,737 issued to S. Billenstein describes and claims softening concentrates containing 30 - 70% of a cationic softener, 5 - 50% of a non-ionic softener, 5 - 20% of a non-ionic dispersing agent, 5 - 30% of a C1 to C3 alkanol, 5 - 30% of liquid glycol, polyglycol or alkyl ether and water and optionally perfume and dyestuffs The fabric softener prepared according to this patent is alleged to be easily dispersible in water.
U.S 4,569,800 issued to K.D. Stanley et al. teaches the use of hydrogenated tallowalkyl 2-ethylhexyl dimethylammonium salts dissolved in water and/or ethanol or in isopropanol in fabric softener compositions These compositions are clear because they form true solutions While consumer preference favors clarity in fabric softener compositions, fabric softeners are preferably brought into contact with the fabric as macroemulsions
It is an object of this invention to provide a clear liquid fabric softener composition that is environmentally acceptable
It is another object to provide such a fabric softener composition as an aqueous microemulsion concentrate.
It is also an object that this microemulsion composition be physically stable for at least about six weeks. Another object is to provide a microemulsion which upon dilution, as in a washing machine dispenser, forms a macroemulsion without gelification.
Other objects will become apparent to those skilled in the art upon a further reading of the specification
SUMMARY OF THE INVENTION
The objects cited above have been satisfied by a clear fabric softener composition comprising an aqueous microemulsion concentrate of (A) (i) a diester quaternary ammonium surfactant fabric softener selected from the group having the structural formulae as follows.
(1 )
(+) (R")4-n - N - (R-A)n X"
wherein each
A is independently C (O) O - R' or - O (O) - C - R',
R is a lower alkyl group having 1 to about 4 carbon atoms,
R' is an alkyl or alkenyl group having 8 to about 22 carbon atoms; R" is independently a lower alkyl radical having 1 to about 6 carbon atoms or hydroxyl alkyl group or H, n is an integer having a value of 1 to about 3,
X" is a softener compatible anion, preferably selected from the group consisting of halide ion and methyl or ethyl sulfate; and
(2)
(R") - N - (R)n - <B)2 wherein B independently is A or (R)n- A; and A, R, R" and n are as defined above; and
(3)
+
(R")3 - N- (R)„— R - R
I I x- A A
wherein A, R, R" and n are as defined above; and/or
(ii) a diamido ammonium surfactant fabric softener having the formula:
O H ^' H O
II I ! I II
R' — C- N- R -N -R -N- C- R'
I (R0)πH X"
wherein n, X" and R' are as defined above, R1 is a lower alkyl radical having 1 to about 4 carbon atoms or hydrogen, and R is an alkylene radical having 2 to about 4 carbon atoms, (B) an organic solvent,
(C) an optional water-immiscible oil perfume, and
(D) an optional fabric co-softener selected from the group consisting of fatty alcohols, fatty acids, fatty esters, fatty amines or amine/amides, whereby said microemulsion is convertible to a milky macroemulsion upon dilution with water. All of the ingredients of the composition delineated above, both required and optional, must be normally liquid, i.e., liquid at ambient room temperatures.
The preferred concentration of softeners in these microemulsions lies between about 40% and about 60% although as little as 10% can be used.
The microemulsion compositions of this invention can contain about 10% to about 60% of the primary softeners, diester quaternary ammonium surfactants and diamido ammonium surfactants, about 5% to about 40% of organic solvent, from 0 to about 15% of co-softener and 0 to about 10% of oil perfume, and the remainder water all on a 100% weight basis.
Most of the prior art quaternary ammonium compounds, commonly designated as Quats, are not environmentally friendly because of their toxicity to aquatic life and/or their poor biodegradability However the softeners of this invention, both the dioleyl diester Quats and the diamido ammonium compounds are environmentally friendly.
Diester quaternary ammonium surfactant fabric softeners, represented by equation (1 ) are commercially available from Stepan Co. as Stepantex and from KAO Corp. as Tetranyl but can also be synthesized by the reaction of two moles of a fatty acid with a trialkanolamine followed by alkoxylation and methylation with dimethyl sulfate or an alkyl halide such as, methyl iodide. In a preferred mode the fatty acid is oleic acid and ethylene oxide is used as the alkoxylation agent. For economical reasons it has been found that Soya fatty acids are a practical source for this purpose consisting of about 3% myristic acid, about 5% palmitic acid, about 5% palmitoleic acid, 1.5% stearic acid, 72.5% oleic acid and about 13% linoleic acid. Other sources of useful fatty acids are those obtained from the saponification of beef tallow, butter, corn oil, cottonseed oil. lard, olive oil, palm oil, peanut oil, cod liver oil, coconut oil and the like. A preferred diester quaternary ammonium surfactant fabric softener is methyl bis[ethyl(oleyl)]-2-hydroxyethyl ammonium methyl sulfate. Other diesters useful in the practice of this invention include: methyl bis-[ethyl(coconut)]-2-hydroxyethyl ammonium methyl sulfate methyl bis-[ethyl(decyl)]-2-hydroxyethyl ammonium methyl sulfate methyl bis-[ethyl(dodecyl)]-2-hydroxyethyl ammonium methyl sulfate methyl bis-[ethyl(lauryl)]-2-hydroxyethyl ammonium methyl sulfate methyl bis-[ethyl(palmityl)]-2-hydroxyethyl ammonium methyl sulfate methyl bis-[ethyl(soft-tallow)]-2-hydroxyethyl ammonium methyl sulfate, and the like. The designation of the terms coconut and soft-tallow indicate mixtures of esters corresponding to the fatty acid source.
In the preparation of the diester quaternary ammonium surfactants, a certain amount of the triester homolog may be produced as an impurity. Unlike the diester, it is not soluble in water and has to be considered as an oil to be emulsified.
A preferred diamido ammonium surfactant fabric softener is the methyl bis- (oleyl amido ethyl)-2-hydroxyethyl ammonium methyl sulfate, a quaternary. This can be synthesized by the interaction of one mole of triethylamine with two moles of oleic acid followed by ethoxylation with ethylene oxide and methylation with dimethyl sulfate. As in the case of the preparation of the diester compounds above, either pure fatty acids or mixtures obtained from the saponification of natural fats and oils can be utilized in their synthesis. These diamido quaternary ammonium surfactant fabric softeners are also commercially from Rewo as Rewopo P.
Another preferred diamido ammonium surfactant fabric softener is the diOleyl diamido amine having the structure O H H °
II I - | II
Oleyl - C-N- (CH^- N- (CH^- N~ C~ Oleyl
(CH2H4 - O -) 2 5 - H
The term "perfume" is used in its ordinary sense to refer to and include any non water-soluble fragrant substance or mixture of substances including natural (i e , obtained by extraction of flower herb, blossom or plant), artificial (i.e., a mixture of natural oils or oil constituents) and synthetic (i e , a single or mixture of synthetically produced substance) odoriferous substances Typically perfumes are complex mixtures of blends of various organic compounds, such as, esters, ketones, hydrocarbons, lactones, alcohols, aldehydes ethers, aromatic compounds and varying amounts of essential oils (e g terpenes) such as from about 0% to about 80%, usually from about 10% to 70% by weight, the essential oils themselves being volatile odoriferous compounds and also serving to dissolve the other components of the perfume The precise composition of the perfume has no particular effect on fabπc softening so long as it meets the criteria of water immiscibility and pleasant odor
Organic solvents suitable for use in this invention include, aliphatic alcohols having 1 to about 6 carbon atoms, such as ethanol, propanol, isopropanol, n- butanol, isobutanol, t-butanol, n-pentanol isopentanol, sec-pentanol, n-hexanol, isohexanol other isomers and the like aliphatic polyalcohols, such as, ethylene glycol, propylene glycol, butylene glycol diethylene glycol, dipropylene glycol, 1 ,4- butanediol 2-methyl-pentanedιol, hexane tπol tπpropylene glycol, pentaerythπtol, glycerol sorbitol, and the like; aliphatic ethers, such as, ethylene glycol monobutyl ether(EGMBE), diethylene glycol monobutyl ether(DEGMBE), diethylene glycol dimethyl ether, tπethylene dimethyl ether, ethylene glycol monomethyl ether, propylene glycol monoethyl ether, dipropylene glycol monomethyl ether, dipropylene glycolpropyl ether(DPnP), dipropylene glycolbutyl ether(DPnB), tnpropylene glycol monomethyl ether, methoxy methyl butanol, and the like, aliphatic esters, such as, methyl lactate, ethyl lactate, isopropyl lactate butyl iactate, dibasic esters of carboxylic acids, ethoxy ethyl acetate propylene glycol butyl ether acetate, and butoxy ethyl acetate
Suitable fabric co-softeners include such fatty acids as lauric acid, palmitic acid, soft-tallow acid, oleic acid, and the like such fatty alcohols as lauryl alcohol, palmityl alcohol, soft-tallowyl alcohol oleyl alcohol and the like, such fatty esters as glycerol mono oleate, glycerol di oleate, pentaerythπtol mono oleate, sorbitan oleate sucrose oleate, as well as these fatty esters where the oleate moiety is replaced by coconut, lauryl or palmityl moieties, and the like, such fatty amines as di- (ethyl-lauryl)-2-hydroxyethyl amine dι-(ethyl-soft tallow)-2-hydroxyethyl amine, and the like, and such amidoammes as dι-coconut-amιdo-ethyl-2-hydroxyethyl amine, dι-lauryl-amιdo-ethyl-2-hydroxyethylamιne, di-soft tallow-amido-ethyl-2- hydroxyethylamine and the like
The clear microemulsions of this invention have a particle size between about 10 and about 100 nanometers They also permit formulation of fabric softeners in a concentrated form amounting to about 10% to about 60% by weight of the total composition These microemulsions are shelf stable remaining as such for at least six weeks After dilution with water, either to obtain a water dispersion of about 4 to about 6% in a bottle or to obtain a rinse liquor containing about 0.2 g. of active softener per liter in the washing machine these microemulsions are converted to milky macroemulsions having a particle size of about 0 1 to about 100 micrometers in which form the softeners readily effect softening of the washed articles The step of conversion from microemulsion to macroemulsion is achieved without gelification. No special equipment is required to combine the components of these microemulsions Mixing equipment known to those skilled in the art suffices It will be also understood by those skilled in this art that the above-described composition may additionally contain as optional components such materials as dyes, foam controllers, thickeners and the like
The invention is further described in the examples which follow All parts and percentages are by weight unless otherwise specified
EXAMPLE 1. Preparation of Softener with a Dioleyl Diester Quaternary
A microemulsion was prepared by mixing 48 03 parts of water, 21.2 parts of hexyleneglycol, 2 5 parts of Dobanol 91 -8 (trade name for a nonionic surfactant alkanol having 9 to 11 carbon atoms and 8 ethoxyl groups from Shell Chemical Co ),
1 27 parts of an oil containing perfume and methylbιs-[ethyl(oleyl)]-2-hydroxyethyl ammonium methyl sulfate represented by the formula O R" O
II I II
C17H33- C- O- R- N- R- O- C- C17- H 33
I ROH
R"S04 "
wherein R= -C2H4- and R"= -CH3. The mixing operation was carried out in a beaker equipped with an electric mixer and a 4-blade impeller. A water clear microemulsion was obtained which remained stable for at least six weeks and which turned into a milky macroemulsion upon dilution with water. A dilution of about 1 part microemulsion to 1000 parts water suffices
Example 2 is a repetition of Example 1 with the exception that no oil containing perfume was charged to the mixer In this combination the microemulsion dephased and did not afford a stable microemulsion.
Examples 3-6. Influence of Organic Solvent
The procedure described in Example 1 was repeated with varying amounts of the organic solvent component. The relevant data are presented in Table 1 below with physical observations of the resultant products.
The table above shows the influence of the organic solvent in a composition containing only Dioleyi Diester Quat and water These data demonstrate the selection of suitable solvents for the preparation of microemulsions of particular combinations of softener and solvent Here it is demonstrated that hexylene glycol and butanol are preferred solvents. EGMBE (Example 4) upon dilution with water leads to a clear solution instead of the desired result, viz., a macroemulsion which is necessary for softening fabrics. Isopropyi lactate is an unsatisfactory solvent in this system since it causes dephasing upon aging even though it provides a clear microemulsion and a turbid macroemulsion
Examples 7-10. Effects of Other Organic Solvents
The effects of using a lower glycol, an ether alkanol, a higher alkyl lactate and an alkanol with Dioleyi Diester Quat to form a microemulsion were studied. The pertinent data shown in Table 2 below indicate that these combinations have limitations here.
Certain generalizations may be inferred from a comparison within solvent classes as to which solvents used in the preceding Examples give stable clear microemulsions and which give unstable products with Dioleyi Diester Quat. These are presented in TABLE 3 below In addition stability also depends on the levels of solvent and Dioleyi Diester Quat used in the examples.
TABLE 3
Solvent Stable Clear Unstable
Class Microemulsion Microemulsion
Glycols Hexylene glycol Ethylene glycol
Ethers EGMBE Methylmethoxybutanol
Esters Isopropyi lactate Butyl lactate
Alkanols Ethanol. butanol Examples 11-13. Effects of Co-Surfactant
The preparation of microemulsions was attempted using the procedure of Example 1 with the addition of a co-surfactant, viz., oleyl alcohol. The results are correlated in TABLE 4 below
As can be seen from the results above, the addition of the co-surfactant, oleyl alcohol modifies the selection of solvents used above for generating a clear microemulsion Thus hexylene glycol leads to a clear gel not a microemulsion. Isopropyi lactate is the best of the three while EGMBE is rejected as in Example 4 for not affording a milky macroemulsion upon dilution In a further extension of this invention it was found that hexylene glycol can be adapted in Example 11 to provide a clear microemulsion by the addition of 0 1 part of nitπlo tπ-methylene phosphonic acid available from Protex Co as Masquol P320 and having the structure
N ≡(CH2PO,H2h
Example 12 demonstrates the necessity for having a turbid macroemulsion after dilution with water inasmuch as it demonstrated poor fabπc softening. Softening efficacy of these compositions was measured through evaluation versus known softening control substances The evaluation procedure was carried out in paired comparison tests among six judges Fabrics treated with test substances are compared against the control substances by their presentation to judges. The judges are asked to score the softness difference between the respective samples on a scale from 0 (no difference) to 3 (very high difference) For example, the microemulsion of Example 1 at a liquor concentration of 0 2375 g/L (45%) was found to be the equivalent of a reference known softening agent consisting of a dispersion of 0.2 g/L (4.5%) of distearyl dimethyl ammonium chloride by this evaluation technique
EXAMPLES 14-17. Addition of Co-softening Agents
Co-softening agents were evaluated in the instant inventive compositions. The amounts of ingredients and physical results are presented in TABLE 5 below
Table 5
Example 14 | Example 15 Example 16 Example 17
Water 56.6 56.6 56.6 56.6
Isopropyi Alchohol 25 25 25 25
Glycerol MonoOleate 3 4 Sorbitan TnOleate 3 4 Polyethylene Glycol- 600 - MonoOleate 3.4 Sucrose Cocoate 3.4 Dioleyi Diester Quat 15 1 15 15 15
Aspect of composition Clear | Turbid Clear Clear
Aspect after dilution Turbid , Turbid Turbid Turbid Emulsion | Emulsion Emulsion Emulsion
Stability Stable 6W Dephasing Stable 6W Stable 6W
Examples 14 to 17 relate to the addition of co-softening ingredients to the primary softener, DiOleyl Diester Quat The structure of Glycerol MonoOleate is self evident from the name, where one hydroxyl group of glycerol was esterified with one mole of oleic acid. Polyethylene Glycol 600-MonoOleate is a polyethylene glycol having an approximate molecular weight of 600 esterified with one mole of oleic acid The structure of Sucrose cocoate is given below
Sorbitan tπOleate is a product obtained by esteπfing one mole of sorbitol with three moles of oleic acid All of these co-softeners are liquid at room temperature and contain olefinically unsaturated aliphatic chains The selected solvent here is isopropyi alcohol and the level of the Dioleyi Diester Quat is reduced taking advantage of the fact that the inclusion of the co-softeners provides a synergistic softening and emulsifying effect Glycerol monoOleate, Polyethylene Glycol-600 monoOleate, and sucrose cocoate afford stable microemulsions. If the number of alkenyl chains increases (HLB), the system does not lead to a microemulsion but to an unstable macro-emulsion
EXAMPLES 18-21. Emulsification of DiOleyl DiAmido Amine
A DiOleyl DiAmido Amine having the structure
O H H O
II I
Oleyl " C-N- (CH^- N- (CH^- N~ C~ Oleyl
( CH2H4 - 0 -) 2 5 - H
was emulsified to a microemulsion after conversion to a salt using the procedure of Example 1 The salt was prepared by neutralization of the free amine with Hydrochloric acid (25%), maleic acid, or lactic respectively The ingredients used and the physical results are given in TABLE 6 below
The neutralizing acid determined whether or not microemulsification took place. Maleic acid gave satisfactory results here while hydrochloric acid and lactic acid did not When the amine was not neutralized (Example 18) no emulsification at all took place.
EXAMPLES 22-24. Solvent Effect
The role of the solvent was demonstrated in a study of the microemulsification of the Dioleyi Diamidoamine/maleic acid system Pertinent data are presented in TABLE 7 together with the data from previously shown Example 20.
Hexylene glycol and DEGMBE can be seen from the above data to be preferred solvents for this system regarding the formation and stability of a microemulsion. Tert-butanol and EGMBE do not stabilize the emulsion which dephases
EXAMPLES 25-28. Stabilization of Synergistic Mixture
Examples relate to the stabilization of the synergistic mixture of DiOleylDiester Quat and DiOleylDiAmidoAmine The materials investigated are presented in TABLE 8 below.
In the series represented in Examples 25-28, n-butanol is the preferred solvent. A gel rather than a clear microemulsion was obtained with hexyleneglycol although the desired effect is obtained with the addition of 0.1 parts of Masquol P320 The addition of Dobanol 91-8 emulsifier did not help to avoid the formation of gels here but rather led to dephasing
EXAMPLES 29-32. Use of DiOleyl Diester Quat Softener
Examples 29-32 relate to the use of DiOleyl Diester Quat with n-butanol as a solvent at several concentration levels The data obtained are displayed in TABLE 9 below
These data demonstrate that microemulsions in the range of about 10% to about 35% were obtainable with n-butanol and that the level of solvent required to produce a microemulsion is not proportional to the level of active ingredient, but surprisingly, the ratio of solvent to dioleyi diester quat decreases when the level of active ingredient increases In Example 32 the ratio is 0 74 In Example 29 the ration is 0 51
It will be appreciated by those in this skilled in this art that not all possible combinations of the various components of this invention falling within the purview of the ranges given will completely satisfy every imaginable end result. Although the invention has been described with a certain amount of particularity, it is understood that the present disclosure of the preferred forms has been made only by way of example and that numerous changes and modifications can be made without departing from the spirit and scope of the invention

Claims (27)

  1. What is claimed is
    1 A clear fabric softener aqueous microemulsion concentrate composition capable of conversion to a macroemulsion upon dilution with water comprising: (A) (i) a diester quaternary ammonium surfactant fabric softener selected from the group having the structural formulae as follows:
    (1 )
    (+) (R")4-n — N - (R-A)n X"
    wherein each
    A is independently C (O) O - R' or _ O (O) - C - R'; R is a lower alkyl group having 1 to about 4 carbon atoms; R' is an alkyl or alkenyl group having 8 to about 22 carbon atoms; R" is independently a lower alkyl radical having 1 to about 6 carbon atoms or hydroxyl alkyl group or H, n is an integer having a value of 1 to about 3, and X" is a softener compatible anion, and
    (2)
    4-
    (R") - N - (R)n - (B)2 X-
    wherein B is independently A or (R)n- A and A, R, R" and n are as defined above; and
    (3)
    -+-
    (R")3 - N— (R)„— R — R
    I I x-
    A A
    wherein A R, R" and n are as defined above, and/or
    (II) a diamido ammonium surfactant fabric softener having the formula- O H ? H O
    II ι I ι ιι
    R' - C - N- R -N -R - N - C- R I (RO)nH X-
    wherem n, X" and R' are as defined above, R"1 is a lower alkyl radical having 1 to about 4 carbon atoms or hydrogen, and R is an alkylene radical having 2 to about 4 carbon atoms,
    (B) an organic solvent,
    (C) an optional water-immiscible oil perfume, and
    (D) an optional fabric co-softener selected from the group consisting of fatty alcohols, fatty acids, fatty esters, fatty amines or amine/amides, whereby said microemulsion is converted to a milky macroemulsion upon dilution with water.
  2. 2 Composition claimed in claim 1 wherein the fabric softener is a diester quaternary ammonium surfactant.
  3. 3 Composition claimed in claim 2 wherein the diester is methyl bis[ethyl(oleyl)]-2-hydroxyethyl ammonium methyl sulfate.
  4. 4 Composition claimed in claim 1 wherein the fabric softener is a combination of a diester quaternary ammonium surfactant and a diamido ammonium surfactant
  5. 5 Composition claimed in claim 4 wherein the diamido ammonium surfactant is methyl bιs-(oleyl amido ethyl)-2-hydroxyethyl ammonium methyl sulfate.
  6. 6 Composition claimed in claim 4 wherein the diamido ammonium surfactant is a salt of a diOleyl diamido amine.
  7. 7 Composition claimed in claim 1 wherein the fabric softener is a diamido ammonium surfactant.
  8. 8 Composition claimed in claim 7 wherein the diamido ammonium surfactant is methyl bιs-(oleyl amido ethyl)-2-hydroxyethyl ammonium methyl sulfate
  9. 9 Composition claimed in claim 7 wherein the diamido ammonium surfactant is a salt of a dioleyi diamino amine
  10. 10 Composition claimed in claim 9 wherein the salt is a salt of maleic acid.
  11. 1 1 Composition claimed in claim 1 wherein said composition contains a water-immiscible oil-perfume.
  12. 12 Composition claimed in claim 1 wherein the organic solvent is a lower alkanol
  13. 13 Composition claimed in claim 12 wherein the alkanol is isopropyi alcohol.
  14. 14 Composition claimed in claim 12 wherein the alkanol is a butanol.
  15. 15 Composition claimed in claim 1 wherein the organic solvent is a glycol.
  16. 16 Composition claimed in claim 15 wherein the glycol is hexylene glycol.
  17. 17 Composition claimed in claim 1 wherein the organic solvent is an aliphatic ether
  18. 18 Composition claimed in claim 17 wherein the aliphatic ether is ethylene or diethylene glycol monobutyl ether
  19. 19 Composition claimed in claim 17 wherein the aliphatic ether is dipropylene glycol methyl ether
  20. 20 Composition claimed in claim 17 wherein the aliphatic ether is dipropylene glycol butyl ether
  21. 21 Composition claimed in claim 1 wherein the fabric co-softener is a fatty alcohol
  22. 22 Composition claimed in claim 21 wherein the fatty alcohol is oleyl alcohol
  23. 23 Composition claimed in claim 1 wherein the fabric softener is a fatty ester.
  24. 24. Composition claimed in claim 23 wherein the fatty ester is glycerol monooleate.
  25. 25 Composition claimed in claim 23 wherein the fatty ester is a polyethylene glycol monooleate.
  26. 26 Composition claimed in claim 23 wherein the fatty ester is sucrose cocoate.
  27. 27. Composition claimed in claim 1 comprising about 10% to about 60% by weight of softener (A), and about 5% to about 40% of organic solvent, with the remainder being water.
    28 Composition claimed in claim 27 comprising in addition up to about 15% of a co-softener and up to about 10% of an oil perfume
AU32172/97A 1994-12-21 1997-05-28 Clear, concentrated liquid fabric softener compositions Ceased AU737508B2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US361350 1994-12-21
AU45250/96A AU691720B2 (en) 1994-12-21 1995-12-19 Clear, concentrated liquid fabric softener compositions
US08/662714 1996-06-10
US08/662,714 US5656585A (en) 1994-12-21 1996-06-10 Clear, concentrated liquid fabric softener compositions
PCT/US1997/009063 WO1997047723A2 (en) 1996-06-10 1997-05-28 Clear, concentrated liquid fabric softener compositions

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
AU45250/96A Division AU691720B2 (en) 1994-12-21 1995-12-19 Clear, concentrated liquid fabric softener compositions

Publications (2)

Publication Number Publication Date
AU3217297A true AU3217297A (en) 1998-01-07
AU737508B2 AU737508B2 (en) 2001-08-23

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
AU32172/97A Ceased AU737508B2 (en) 1994-12-21 1997-05-28 Clear, concentrated liquid fabric softener compositions

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Country Link
AU (1) AU737508B2 (en)

Also Published As

Publication number Publication date
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