Fabric conditioning compositions

Abstract

A liquid fabric softening composition comprising: i) an aqueous continuous phase; ii) a disperse phase comprising a cationic softening agent; iii) a nonionic surfactant; and iv) an associative thickener, wherein the disperse phase has a phase volume of 0.75 or less and the cationic softening agent comprises 5% or greater by weight of the total composition.

Description

FIELD OF THE INVENTION

The present invention relates to fabric conditioning compositions. More specifically, the invention relates to thick and creamy fabric softening compositions comprising a softener of low phase volume and an associative thickener.

BACKGROUND OF THE INVENTION

It is well known to provide liquid fabric conditioning compositions that soften treated fabric, i.e. liquid fabric softeners. Such compositions are typically added to fabric in the rinse cycle of the wash process. Consumer preference is for liquid fabric softeners that are thick and creamy; however, attaining this goal can lead to problems, particularly with regard to the dispensing and storage stability of the composition. It is often found that thick and creamy liquid softeners dispense poorly; this can lead to wasted product and, when used in automatic washing machines, messy residues being left the dispenser draw of the machine. A further problem associated with thick and creamy fabric softeners is poor storage stability, the desirable rheological properties of the composition being lost upon storage. A particularly common rheological problem is product thickening on storage, especially at elevated temperature or low temperature.

EP 331,237 (Unilever, 1989) discloses liquid fabric softeners comprising thickening polymers that act as associative thickeners. However, this publication does not disclose compositions comprising 5% or greater of cationic. softening agent having a phase structure adjusted by nonionic surfactant and having a phase volume of less than 0.75, nor does it suggest the benefits that such micro-structure can lead to in liquid softeners comprising cationic softening agent and associative thickener (vide infra).

Numerous publications disclose liquid fabric softeners comprising a cationic softening agent and a nonionic surfactant, an example being EP 523,922 B1 (Unilever, 1992). WO 03/012019 (Unilever, 2002) also discloses associative thickener as an optional component; however, compositions comprising 5% or greater of cationic softening agent having a phase volume of less than 0.75 are not disclosed nor envisaged. WO 01/46360 (Unilever, 2000) discloses liquid fabric softeners comprising a cationic softening agent, a nonionic surfactant and an optional associative thickener; however, this publication is also silent regarding systems comprising 5% or greater of cationic softening agent that have a phase volume of less than 0.75.

OBJECTS OF THE INVENTION

It is an object of the present invention to provide a fabric conditioning composition that appears thick and creamy and yet dispenses efficiently and gives a good degree of softness to treated fabrics. It is a further object of the present invention to provide a fabric conditioning composition having the aforementioned benefits and good storage stability.

SUMMARY OF THE INVENTION

According to a first aspect of the present invention, there is provided a liquid fabric softening composition comprising:

• i). an aqueous continuous phase;
• ii). a disperse phase comprising a cationic softening agent;
• iii). a nonionic surfactant; and
• iv). an associative thickener,
  wherein the disperse phase has a phase volume of 0.75 or less and the cationic softening agent comprises 5% or greater by weight of the total composition.

According to a second aspect of the present invention, there is provided a method for the treatment of fabrics comprising contacting fabrics with a liquid fabric softening composition according to the first aspect of the invention or any of the particular variants thereof disclosed in the following description.

According to a third aspect of the present invention, there is provided a method for the manufacture of a liquid fabric softening composition comprising the steps of dispersing a cationic softening agent and a nonionic surfactant in an aqueous continuous phase, reducing the phase volume of the disperse phase, and using an associative thickener to thicken the composition, wherein the disperse phase is reduced to a phase volume of 0.75 or less and the cationic softening agent comprises 5% or greater of the total composition.

In the context of the present invention, the term “comprising” means “including” and is non-exhaustive.

DETAILED DESCRIPTION OF THE INVENTION

The compositions of the invention are highly effective fabric softeners, having 5% or greater by weight of cationic softening agent present. They appear thick and creamy and yet have surprisingly good storage stability and dispensing efficiency, leaving little or no residue in the conditioner portion of the dispenser draw of a conventional automatic washing machine. It is believed that the combination of a disperse phase comprising 5% or greater cationic softening agent and a phase volume of 0.75 or less, an associative thickener, and a non-ionic surfactant leads to a product micro-structure that enables the above benefits to be attained. The product micro-structure is believed to comprise dispersed fragments of cationic softening agent, generally in lamellar phase, stabilised by nonionic surfactant and linked together, under low shear conditions (for example, at shear rates of from 2 to 20/s), by the associative thickener.

The benefits given by the compositions of the invention relate to their rheological properties. At a shear rate relevant to the pouring of the composition from a bottle, it is important that the composition appears thick and creamy—at such a shear rate, for example at 20/s, the viscosity of the composition is preferably from 200 to 450 mPa.s. At lower shear rates such as 2/s, which are believed to be relevant to the dispensing of the formulation, the composition may have a viscosity as high as from 600 to 1100 mPa.s and yet still dispense efficiently. At higher shear rates, however, the composition will generally have a lower viscosity—at 106/s it is preferred that the viscosity is from 90 to 200 mPa.s.

Throughout this specification it should be understood that all values requiring measurement, in particular viscosity values, relate to measurements made at 20° C. and 1 atmosphere pressure.

By measuring the viscosity (η) at a range of shear rates (γ) it is possible to obtain a value for the infinite shear rate viscosity (η_∞) of a composition by using the Sisco model:
η=η_∞+Kγⁿ⁻¹
where ‘K’ is the consistency and ‘n’ is the power law index.

The infinite shear rate viscosity may then be used to obtain a value for the phase volume () of a disperse phase within a composition as a whole by using a Kreigher-Dougherty equation:
η_∞=η_c(1−/_m)⁻²
where η_c is the viscosity of the continuous phase and _m is the maximum volume fraction; the values of both of these terms can be equated to unity for the aqueous based liquid compositions of the present invention.

Details of the above equations and their usage may be found in basic rheology textbooks such as “Rheology for Chemists, An Introduction”, by J. W. Goodwin and R. W. Hughes, published by the Royal Society of Chemists in 2000 and “Colloidal Dispersions” by W. B. Russel et al, published by Cambridge University Press in 1989.

The phase volume of the disperse phase may be thought of as the volume of the total composition occupied by the disperse phase at infinite shear rate. The compositions of the present invention have a phase volume of 0.75 or less. Only at such low phase volumes can the desired efficiency of dispensing be attained. The phase volume is preferably 0.70 or less. Fabric softening compositions comprising 5% or greater of cationic softening agent do not generally have such low phase volumes, unless induced by processing and/or the additives.

The Cationic Softening Agent

The cationic softening agent is typically a quaternary ammonium compound (“QAC”), in particular one having two C_12-28 groups connected to the nitrogen head group that may independently be alkyl or alkenyl groups, preferably being connected to the nitrogen head group by at least one ester link, and more preferably by two ester links.

The average chain length of the alkyl and/or alkenyl groups is preferably at least C₁₄ and more preferably at least C₁₆. It is particularly preferred that at least half of the groups have a chain length of C₁₈. In general, the alkyl and/or alkenyl groups are predominantly linear.

A first group of QACs suitable for use in the present invention is represented by formula (I):
wherein each R is independently selected from a C_5-35 alkyl or alkenyl group; R¹ represents a C_1-4 alkyl, C_2-4 alkenyl or a C_1-4 hydroxyalkyl group; T is generally O—CO. (i.e. an ester group bound to R via its carbon atom), but may alternatively be CO.O (i.e. an ester group bound to R via its oxygen atom); n is a number selected from 1 to 4; m is a number selected from 1, 2, or 3; and X⁻ is an anionic counter-ion, such as a halide or alkyl sulphate, e.g. chloride or methylsulphate. Di-esters variants of formula I (i.e. m=2) are preferred and typically have mono- and tri-ester analogues associated with them. Such materials are particularly suitable for use in the present invention.

Especially preferred agents are di-esters of triethanolammonium methylsulphate, otherwise referred to as “TEA ester quats.”. Commercial examples include Prapagen TQL, ex Clariant, and Tetranyl AHT-1, ex Kao, (both di-[hardened tallow ester] of triethanolammonium methylsulphate), AT-1 (di-[tallow ester] of triethanolammonium methylsulphate), and L5/90 (di-[palm ester] of triethanolammonium methylsulphate), both ex Kao, and Rewoquat WE15 (a di-ester of triethanolammonium methylsulphate having fatty acyl residues deriving from C₁₀-C₂₀ and C₁₆-C₁₈ unsaturated fatty acids), ex Witco Corporation.

The second group of QACs suitable for use in the invention is represented by formula (II):
wherein each R¹ group is independently selected from C_1-4 alkyl, hydroxyalkyl or C_2-4 alkenyl groups; and wherein each R² group is independently selected from C_8-28 alkyl or alkenyl groups; and wherein n, T, and X⁻ are as defined above.

Preferred materials of this second group include 1,2 bis[tallowoyloxy]-3-trimethylammonium propane chloride, 1,2 bis [hardened tallowoyloxy]-3-trimethylammonium propane chloride, 1,2-bis [oleoyloxy]-3-trimethylammonium propane chloride, and 1,2 bis [stearoyloxy]-3-trimethylammonium propane chloride. Such materials are described in U.S. Pat. No. 4,137,180 (Lever Brothers). Preferably, these materials also comprise an amount of the corresponding mono-ester.

A third group of QACs suitable for use in the invention is represented by formula (III):
(R¹)₂—N⁺—[(CH₂)_n-T-R²]₂X⁻  (III)
wherein each R¹ group is independently selected from C_1-4 alkyl, or C_2-4 alkenyl groups; and wherein each R² group is independently selected from C_8-28 alkyl or alkenyl groups; and n, T, and X⁻ are as defined above. Preferred materials of this third group include bis(2-tallowoyloxyethyl)dimethyl ammonium chloride and hardened versions thereof.

A fourth group of QACs suitable for use in the invention is represented by formula (IV):
(R¹)₂—N⁺—(R²)₂X⁻  (IV)
wherein each R² group is independently selected from C_1-4 alkyl, or C_2-4 alkenyl groups; and wherein each R² group is independently selected from C_8-28 alkyl or alkenyl groups; and X⁻ is as defined above. Preferred materials of this fourth group include di(hardened tallow)dimethylammonium chloride.

The iodine value of the softening agent is preferably from 0 to 20, more preferably from 0 to 4, and most preferably from 0 to 2. Essentially saturated material, i.e. having an iodine value of from 0 to 1, is used in especially high performing compositions. At low iodine values, the softening performance is excellent and the composition has improved resistance to oxidation and associated odour problems upon storage. To optimise the properties of compositions having agents of low iodine value, it is preferred that the level and nature of the nonionic surfactant are carefully selected (vide infra).

Iodine value is defined as the number of grams of iodine absorbed per 100 g of test material. NMR spectroscopy is a suitable technique for determining the iodine value of the softening agents of the present invention, using the method described in Anal. Chem., 34, 1136 (1962) by Johnson and Shoolery and in EP 593,542 (Unilever, 1993).

The softening agent is present in the compositions of the invention at a level of 5% or greater by weight of the total composition. For even greater softening effect, this level may be 8% or greater; whilst for particularly high performance, this level may be 11% or greater. At these higher concentrations, which are also desirable for supply chain and environmental reasons, the low dispenser residues found with the compositions of the present invention is particularly relevant and unexpected.

For ease of formulation, the amount of softening agent is generally 50% or less, particularly 40% or less, and especially 30% or less by weight of the total composition.

The Nonionic Surfactant

Suitable nonionic surfactants include alkoxylated materials, particularly addition products of ethylene oxide and/or propylene oxide with fatty alcohols, fatty acids and fatty amines.

Preferred materials are of the general formula:
R—Y—(CH₂CH₂O)_zH
Where R is a hydrophobic moiety, typically being an alkyl or alkenyl group, said group being linear or branched, primary or secondary, and preferably having from 8 to 25, more preferably 10 to 20, and most preferably 10 to 18 carbon atoms; R may also be an aromatic group, such as a phenolic group, substituted by an alkyl or alkenyl group as described above; Y is a linking group, typically being O, CO.O, or CO.N(R¹), where R¹ is H or a C_1-4 alkyl group; and z represents the average number of ethoxylate (EO) units present, said number being 8 or more, preferably 10 or more, and most preferably 15 to 30.

Preferably the nonionic surfactant has an HLB of from 7 to 20, more preferably from 10 to 20, and most preferably from 15 to 20.

Examples of suitable nonionic surfactants include the ethoxylates of mixed natural or synthetic alcohols in the “coco” or “tallow” chain length. Preferred materials are condensation products of coconut fatty alcohol with 15-20 moles of ethylene oxide and condensation products of tallow fatty alcohol with 10-20 moles of ethylene oxide.

The ethoxylates of secondary alcohols such as 3-hexadecanol, 2-octadecanol, 4-eicosanol, and 5-eicosanol may also be used. Exemplary ethoxylated secondary alcohols have formulae C₁₂-EO(20); C₁₄-EO(20); C₁₄-EO(25); and C₁₆-EO(30).

Polyol-based nonionic surfactants may also be used, examples including sucrose esters (such as sucrose monooleate), alkyl polyglucosides (such as stearyl monoglucoside and stearyl triglucoside), and alkyl polyglycerols.

A particular nonionic surfactant may be useful in the present compositions alone or in combination with other nonionic surfactants. The preferred amounts of nonionic surfactant indicated below refer to the total amount of such materials that are present in the composition.

The nonionic surfactant is present in an amount from 0.05 to 10%, more preferably 0.1 to 5%, and most preferably 0.35 to 3.5%, based on the total weight of the composition.

When the softening agent has an iodine value from 0 to 20, particularly from 0 to 4 and especially from 0 to 2, it is preferred that nonionic surfactant having an HLB of 15-20 is present at a level of 0.05% or greater, more preferably 0.1% or greater, and most preferably 0.35% or greater, based on the total weight of the composition.

The Associative Thickener

An associative thickener is an essential component of the compositions of the invention, serving to promote the desired thick and creamy appearance. Suitable associative thickeners may be selected from hydrophobically modified cellulose ethers, as described in GB 2,043,646 (Hercules) and disclosed in fabric conditioning compositions in EP 331,237 B1 (Unilever). Such materials are typically nonionic polymers and have a sufficient degree of nonionic substitution selected from the class consisting of methyl, hydroxyethyl and hydroxypropyl to cause them to be water-soluble and which are further substituted with one or more hydrocarbon radicals having from 10 to 24 carbon atoms, in an amount from 0.2% by weight to an amount which renders the cellulose ether less than 1% by weight soluble in water. The nonionic cellulose ether that forms the ‘backbone’ of the hydrophobically modified derivative may be any nonionic water soluble cellulose ether substrate, such as hydroxyethyl cellulose (HEC), hydroxypropyl cellulose (HPC), methyl cellulose, hydroxypropyl methyl cellulose, ethyl hydroxyethyl cellulose or methyl hydroxyethyl cellulose. The preferred ‘backbone’ is HEC.

Other suitable associative thickeners include the Collacral range (ethoxylate urethanes) from BASF, the PureThix range from Sud-Chemie, the Aquaflow range (HM end-capped PEGs) from Aqualon, and the Nexton range (HMHEC), also from Aqualon.

Especially preferred associative thickeners are hydrophobically modified cellulose ethers sold under the trade names Natrosol Plus 100, 250, 331, and 430, by Hercules.

The molecular weight of the associative thickener is preferably from 1,000 to 1,000,000, more preferably from 50,000 to 500,000 and most preferably from 100,000 to 400,000.

The associative thickener is typically used at a level of at least 0.0005%, in particular at from 0.0005 to 2%, and especially at from 0.001 to 0.5% by weight of the total composition.

Aqueous Continuous Phase

The aqueous continuous phase typically comprises 80% or greater by weight of water; sometimes this figure may rise to 90% or greater, or 95% or greater. The water in the aqueous continuous phase typically comprises 40% or greater by weight of the total formulation; preferably this figure is 60% or greater, more preferably it is 70% or greater.

The aqueous continuous phase may also comprise water-soluble species, such as mineral salts or short chain (C_1-4) alcohols. The mineral salts may aid the attainment of the required phase volume for the composition, as may water soluble organic salts and cationic deflocculating polymers, as described in EP 41,698 A2 (Unilever). Such salts may be present at from 0.001 to 1% and preferably at from 0.005 to 0.1% by weight of the total composition. Examples of suitable mineral salts for this purpose include calcium chloride and magnesium chloride. Short chain alcohols that may be present include primary alcohols, such as ethanol, propanol, and butanol, secondary alcohols such as isopropanol, and polyhydric alcohols such as propylene glycol and glycerol. The short chain alcohol may be added with cationic softening agent during the preparation of the composition.

Fatty Complexing Agent

A highly preferred additional component in the compositions of the present invention is a fatty complexing agent. Such agents typically have a C₈ to C₂₂ hydrocarbyl chain present as part of their molecular structure. Suitable fatty complexing agents include C₈ to C₂₂ fatty alcohols and C₈ to C₂₂ fatty acids; of these, the C₈ to C₂₂ fatty alcohols are most preferred. A fatty complexing agent is particularly valuable in compositions comprising a QAC having a single C_12-28 group connected to the nitrogen head group, such as mono-ester associated with a TEA ester quat. or a softening agent of formula II.

It is thought that the complexing agent may bind to the single chain QAC described above in preference to the nonionic surfactant and thereby free the nonionic surfactant to stabilise the disperse phase and help reduce its phase volume. Complexing the single chain QAC may also aid the rheological stability of the composition in another manner; the presence of such single chain QACs, particular when present at levels of 10 mole % or greater of the total QAC, can lead to depletion flocculation—addition of a complexing agent has the effect of reducing their free concentration, thereby reducing or eliminating this problem. Enhanced softening performance may also result from the presence of the complex formed between the single chain QAC and the complexing agent.

Preferred fatty acid complexing agents include hardened tallow fatty acid (available as Pristerene, ex Uniqema).

Preferred fatty alcohol complexing agents include hardened tallow alcohol (available as Stenol and Hydrenol, ex Cognis, and Laurex CS, ex Albright and Wilson) and behenyl alcohol, a C₂₂ fatty alcohol, available as Lanette 22, ex Henkel.

The fatty complexing agent may be used at from 0.1% to 10%, particularly at from 0.5% to 5%, and especially at from 0.75 to 2% by weight, based on the total weight of the composition.

When a QAC having a single C_12-28 group connected to the nitrogen head group is present, the mole ratio of the fatty complexing agent to said single chain QAC is preferably from 1:3 to 3:1, more preferably 1:2 to 2:1, and most preferably 2:3 to 3:2.

Perfume

The compositions of the invention typically comprise one or more perfumes. The perfume is preferably present in an amount from 0.01 to 10% by weight, more preferably 0.05 to 5% by weight, most preferably 0.5 to 4.0% by weight, based on the total weight of the composition.

Co-Softener

Co-softeners may be used together with the cationic softening agent. When employed, they are typically present at from 0.1 to 20% and particularly at from 0.5 to 10%, based on the total weight of the composition. Preferred co-softeners include fatty esters, and fatty N-oxides.

Fatty esters that may be employed include fatty monoesters, such as glycerol monostearate, fatty sugar esters, such as those disclosed WO 01/46361 (Unilever).

Further Optional Ingredients

The compositions of the invention may contain one or more other ingredients. Such ingredients include preservatives (e.g. bactericides), pH buffering agents, perfume carriers, fluorescers, colourants, hydrotropes, antifoaming agents, anti-redeposition agents, soil-release agents, polyelectrolytes, enzymes, optical brightening agents, anti-shrinking agents, anti-wrinkle agents, anti-spotting agents, anti-oxidants, sunscreens, anti-corrosion agents, drape imparting agents, anti-static agents, ironing aids and dyes.

A particularly preferred optional ingredient is an opacifier or pearlescer. Such ingredients can serve to augment the creamy appearance of the compositions of the invention. Suitable materials may be selected from the Aqusol 0P30X range (ex Rohm and Haas), the PuriColour White range (ex Ciba) and the LameSoft™ range (ex Cognis). Such materials are typically used at a level of from 0.01 to 1% by weight of the total composition.

Product Use

The compositions of the present invention are preferably rinse conditioner compositions and may be used in the rinse cycle of a domestic laundry process.

The composition is preferably used in the rinse cycle of a home textile laundering operation, where, it may be added directly in an undiluted state to a washing machine, e.g. through a dispenser drawer or, for a top-loading washing machine, directly into the drum. Alternatively, it can be diluted prior to use. The compositions may also be used in a domestic hand-washing laundry operation.

It is also possible, though less desirable, for the compositions of the present invention to be used in industrial laundry operations, e.g. as a finishing agent for softening new clothes prior to sale to consumers.

Method of Manufacture

Formulations according to the invention may be prepared by the method of manufacture described as the third aspect of the invention. In this method, the is should be understood that the dispersing of the cationic softening agent and nonionic surfactant in the aqueous continuous phase may involve dissolution of at least some of the nonionic surfactant in the aqueous continuous phase. The required reduction in the phase volume of the disperse phase may be brought about by any of the means known in the art. Such means may comprise the addition of an electrolyte, such as a mineral salt, and/or milling of the formulation. Milling of the formulation, when employed, is typically performed until 50% or greater, in particular 100% or greater and especially 150% or greater of the batch volume has passed through the mill.

In a typical method of manufacture, the cationic softening agent, nonionic surfactant, and any optional hydrophobic components such co-softener are heated together until a co-melt is formed. Water is heated and the co-melt is added to the water with stirring. The phase volume of the disperse phase is reduced by the addition of an electrolyte and/or by milling, preferably whilst the mixture is still hot. When the cationic softening agent is present as a lamellar phase dispersion, it is preferred that milling is carried above the L_α-L_β phase transition temperature. The mixture is then thickened by the addition of associative thickener, typically added as an aqueous solution of concentration from 1 to 2% by weight, and is then allowed to cool.

EXAMPLES

The invention will now be illustrated by the following non-limiting examples. Further modifications will be apparent to the person skilled in the art.

Examples of the invention are represented by a number. Comparative examples are represented by a letter.

TABLE 1
Base Formulation for Examples A to E and 1
		Amount
	Component	(wt. %)
	Prapagen TQL	TEA ester quat., ex Clariant	12.7
	Genapol C200	Coconut alcohol polyglycol	0.4
		ether (20 EO), ex Clariant
	Stenol	Hardened tallow fatty alcohol,	1.0
		ex Cognis
	Perfume		0.7
	Water and		To 100
	minors

The base formulation indicated in Table 1 was prepared by methods standard in the art. The phase volume of the core formulation was then reduced to the levels indicated in Table 2 by shearing the formulation for the number of batch volumes (BV) indicated. Phase volumes were determined by measuring the viscosity at a range of shear rates, using these data to calculate the infinite shear rate viscosity via the Sisco model and then using using the Kreigher-Dougherty equation to get a value for the phase volume from the infinite shear rate viscosity so calculated (vide supra).

Associative thickener (Natrosol Plus 331, ex Hercules) was added to Example E to give Example 1. The sensitivity of the dispensing efficiency to the phase volume is clear from the dispenser residue figures indicated in Table 2. These figures were obtained on use of the indicated formulation in a conventional Miele Novotronic automatic washing machine. These figures indicate that by using a suitable formulation of low phase volume, it is possible to add the associative thickener without major detrimental effect upon the dispensing. The addition of the associative thickener gave a formulation of thick and creamy appearance (viscosity 245 mPa.s at 20/s, in comparison with a value of 71 mPa.s, at the same shear, rate for example E).

TABLE 2
	Polymer	Milling	Phase	Dispenser
Example	wt. %)	(BV)	volume	residue (wt. %)
A	0	0	0.81	52.5
B	0	0.5	0.79	20.9
C	0	1	0.69	4.1
D	0	1.5	0.68	2.5
E	0	2	0.65	2.5
1	0.012	2	0.64	2.9

The phase volume may also be reduced by the addition of mineral salt. Example F (Table 3) was prepared in a similar manner to that used for examples A to E, using 13% of the TEA quat., 0.6% of the nonionic surfactant, 0.6% of the fatty alcohol, and 0.75% of perfume. Calcium chloride and associative thickener were then added to give Examples 2 and 3, as shown in Table 3. The Table also shows the phase volumes for the samples and the dispenser residues resulting from their use in a conventional Miele Novotronic automatic washing machine. Examples 2 and 3 each had a thick and creamy appearance (viscosities at 20/s of 232 mPa.s and 197 mPa.s, respectively) and yet both gave low dispenser residues, in comparison with Example F.

	TABLE 3
		CaCl2	Polymer	Phase	Dispenser
	Example	(wt. %)	(wt. %)	volume	residue (wt. %)
	F	0	0	0.79	25.7
	2	0.01	0.0011	0.70	7.8
	3	0.01	0.0012	0.66	5.3
	1Natrosol Plus 331, ex Hercules, Mw. ca. 370,000.
	2Natrosol Plus 100, ex Hercules.

Examples similar to the above have also been prepared using Natrosol Plus 430 (Mw. ca. 470,000). This material also gave compositions having a thick and creamy appearance, that dispensed without leaving excessive residues; however, it was less weight effective than its lower molecular weight analogues.

In a further series of control experiments, process-thinned compositions were thickened using a continuous phase thickener: Softgel BDA, a cationically modified potato starch, ex Avebe. Thick products could be produced in this manner (having viscosities at 20/s of 290 mPa.s and above), but only at the expense of high dispenser residues (25 wt. % and above), showing the inferiority of continuous phase thickeners when compared with the associative thickeners used in conjunction with the other aspects of the present invention.

Claims

1. A liquid fabric softening composition comprising:

i) an aqueous continuous phase;

ii) a disperse phase comprising a cationic softening agent;

iii) a nonionic surfactant; and

iv) an associative thickener,

wherein the disperse phase has a phase volume of 0.75 or less and the cationic softening agent comprises 5% or greater by weight of the total composition.

2. A fabric softening composition according to claim 1, having a viscosity at 20/s of from 200 to 450 mPa.s.

3. A fabric softening composition according to claim 1, wherein the disperse phase comprises fragments of lamellar phase cationic softening agent stabilised by nonionic surfactant and linked by associative thickener.

4. A fabric softening composition according to claim 1, having a phase volume of 0.70 or less.

5. A fabric softening composition according to claim 1, wherein the cationic softening agent has an iodine value of from 0 to 20, more preferably 0 to 2.

6. A fabric softening composition according to claim 1, wherein the nonionic surfactant has an HLB of from 7 to 20, more preferably 15 to 20.

7. A fabric softening composition according to claim 1, wherein the nonionic surfactant is present at a level of 0.05% or greater, more preferably 0.35% or greater based on the total weight of the composition.

8. A fabric softening composition according to claim 1, wherein the associative thickener is a hydrophobically modified cellulose ether.

9. A fabric softening composition according to claim 1, wherein the associative thickener has a molecular weight of from 50,000 to 500,000.

10. A fabric softening composition according to claim 1, wherein the associative thickener is present at a level of from 0.001 to 0.5% by weight of the total composition.

11. A fabric softening composition according to claim 1, comprising a quaternary ammonium compound having a single C12-28 group connected to the nitrogen head group.

12. A fabric softening composition according to claim 11, wherein the mole ratio of the fatty complexing agent to the quaternary ammonium compound having a single C12-28 group connected to the nitrogen head group is from 1:3 to 3:1.

13. A method for the treatment of fabrics comprising contacting fabrics with a liquid fabric softening composition according to claim 1.

14. A method for the manufacture of a liquid fabric softening composition comprising the steps of dispersing a cationic softening agent and a nonionic surfactant in an aqueous continuous phase, reducing the phase volume of the disperse phase, and using an associative thickener to thicken the composition, wherein the disperse phase is reduced to a phase volume of 0.75 or less and the cationic softening agent comprises 5% or greater of the total composition.

15. A method according to claim 14, wherein the phase volume is reduced by the addition of an electrolyte and/or milling the formulation.