[0001] Fabric conditioners are widely used to soften fabrics after washing in anionic detergents.
As used herein the term refers to cationic organic compounds such as amine salts or
quaternary nitrogen compounds, all of which have two long chain (e.g. C₁₅₋₂₂) alkyl
and/or alkenyl groups, and especially two C₁₆₋₁₈ alkyl and/or alkenyl groups (e.g.
tallowyl, oleyl, palmityl and/or stearyl groups).
[0002] Among the types of fabric conditioners which have been used are included quaternary
ammonium salts and, in particular, distearyl dimethyl ammonium chloride, amido imidazoline
salts, quaternised amido imidazolines, amido amine salts quaternised amido amines
and ethoxylated amido amines. The amido imidazoline salts and quaternised amido imidazolines
may be derived from amido amines by cyclisation. For convenience therefore, amido
amine salts, amido imidazoline salts and their quaternised and/or alkoxylated derivatives
are referred to collectively herein as "amido amine derivatives". Although they are
only very sparingly soluble in water, fabric softeners can be fairly easily dispersed
to form dilute aqueous dispersions with concentrations of up to about 20%. However
a major problem encountered in the handling and formulation of fabric conditioners
is the high viscosity of even the more dilute of such aqueous dispersions.
[0003] This is a particular problem for the manufacturer who supplies cationic fabric conditioners
in bulk to the formulator, since it is difficult to obtain concentrated dispersions
of fabric conditioners in a readily pourable and stable form. The manufacturer is
thus concerned to reduce the viscosity of the bulk products, and at the same time
to maintain and, if possible increase the relative concentration, in order to reduce
the cost and inconvenience of transporting and storing large volumes of water.
[0004] The problem for the formulator is more complicated. There is an obvious need for
a compromise between increased cost per unit volume and greater difficulty in pouring,
on the one hand and increased effectiveness, per unit volume, on the other as the
concentration is increased. However, consideration must also be given to the prejudice
of the consumer who believes that more viscous products are necessarily more concentrated
and therefore more effective, and may purchase a more viscous, but more dilute product
despite its being less cost effective and harder to pour.
[0005] Control of viscosity, both in concentrated products, and on dilution, is therefore
of crucial importance in making and formulating fabric conditioners.
[0006] The formulator normally sells compositions containing 3 to 7% fabric conditioner
which represents the maximum concentration at which the formulation is sufficiently
pourable, although higher concentrations e.g. up to about 15% can be achieved by adding
trace amounts, usually of the order 100 to 1,500ppm, of calcium ion, e.g. as calcium
chloride, which tends to reduce the viscosity. Concentrations greater than about 20%
can only be achieved by using water soluble organic solvents. Manufacturers who need
to achieve concentrations of greater than 50%, preferably 75 to 90%, for efficient
distribution to the formulators, have therefore had to make substantially anhydrous
concentrates in organic solvents such as lower alcohols. In practice the solvent most
commonly used is isopropanol, which is expensive, flammable, odourous and may produce
undesirable effects in the final formulation, such as variation of dispersion viscocity
on ageing. Isopropanol has, however, generally been considered essential to obtain
a pourable and concentrated composition.
[0007] The concentrate containing the water miscible solvents can be dispersed by stirring
in hot water and blended with fatty alcohols, non-ionic surfactants, colouring, perfumes
and traces of soluble calcium salts such as calcium chloride, in order to obtain a
pourable formulation acceptable to the consumer.
[0008] The difficulty of handling concentrates, the need to use hot water and the disadvantages
of solvent, have all led manufacturers for many years to look for alternative ways
of preparing concentrates, but hitherto without success. It is possible to alleviate
some of the problems by using an unsaturated or partly unsaturated feedstock such
as oleyl or soft tallow to provide the long chain alkyl/alkenyl group of the fabric
conditioner and products have been prepared using feedstocks of a high iodine value
(ie high degree of unsaturation).
[0009] Unfortunately it has been found that the higher the iodine value of the feedstock,
the poorer is the fabric softening effect, and the more prone is the product to oxidation
leading to discolouration and malodour.
[0010] We have now discovered a novel physical state of aqueous cationic fabric conditioners
which enables them to be obtained as mobile creams of high concentration. We have
discovered that when electrolytes are included in certain critical concentrations
in aqueous dispersions of cationic fabric conditioners a characteristic spherulitic
structure is obtained, which typically undergoes spontaneous creaming. The cream is
a mobile concentrated aqueous dispersion with good fabric softening properties, which
is rapidly dispersible in cold water by stirring or shaking. It is possible to use
alkyl feedstocks with low iodine values without sacrificing mobility. The rediluted
creams can be obtained in a stable form of satisfactory viscosity.
Creams having a similar structure and composition to those obtained by allowing a
dilute system to cream can also be prepared directly by mixing an electrolyte solution
with the concentrate, until the desired cream concentration is achieved. However the
properties of products so prepared are usually inferior to those obtained by actual
creaming of a diluted solution. They are, nevertheless, within the scope of our invention
and may be preferred in some cases due to their ease of preparation. In general we
have found that creams of our invention can be identified by a characteristic spherulitic
appearance under the optical microscope. The spherulites show crosses when viewed
between cross polarisers. The creams also exhibit characteristic neutron scattering
paterns, with peaks at around 50 and 25 Angstroms.
[0011] According to one embodiment our invention therefore provides a composition comprising:
water and at least one cationic fabric conditioner having two C₁₅₋₂₂ alkyl or alkenyl
groups dispersed in the water, in the presence of dissolved electrolyte in a concentration
sufficient (i) to provide an optically anisotropic spherulitic composition and/or,
(ii) to cause creaming of a more dilute dispersion of said fabric conditioner.
[0012] According to a second embodiment our invention provides a cream formed by the inclusion
of sufficient of a water soluble electrolyte in an aqueous dispersion of a cationic
fabric conditioner, to cause creaming of the dispersed phase, and separating the cream
from remainder of the liquid.
[0013] According to a third embodiment our invention provides a composition comprising water,
a dissolved electrolyte in a concentration greater than 1% by weight of the composition,
and a cationic fabric conditioner comprising at least 40% by weight, based on the
total active weight, of an amido amine derivative having two C₁₅₋₂₂ alkyl or alkenyl
groups dispersed in the aqueous electrolyte as optically anisotropic spherulites in
a concentration between 18 and 50% by weight.
[0014] According to a further embodiment our invention provides a method of manufacture
of a fabric conditioner cream which comprises forming a dispersion in water of at
least one creamable cationic fabric conditioner, in the presence of a water soluble
electrolyte in an amount sufficient to cause the fabric conditioner to cream, and
separating the cream from the remainder of the aqueous dispersion. Preferably the
creaming is accelerated by centrifuging. The dispersion is conveniently formed by
adding a concentrate of the fabric conditioner in a water miscible, organic solvent
to an aqueous electrolyte.
[0015] Alternatively, our invention provides a method of preparing a fabric softener cream
which comprises mixing together an aqueous electrolyte and a solution of from 50 to
80% by weight of a cationic fabric conditioner comprising at least 40% by weight,
based on the total active weight, of an amido amine derivative having two C₁₅₋₂₂ alkyl
or alkenyl groups in a water miscible organic solvent to provide a final electrolyte
concentration of from 1 to 10% by weight of the composition and a fabric conditioner
concentration from 18% to 40% active matter by weight of the composition.
[0016] According to our invention we prefer to use quaternised imidazoline fabric conditioners
having two long chain, e.g. C 15-20, alkyl and/or alkenyl groups such as ditallowyl
or distearyl imidazolinium methosulphate. Unquaternised imidazolinium salts, having
two C15-20 alkyl groups are also useful as are mono or di-alkylated diamidoammonium
salts having two C1-4 alkyl groups and two C15-20 alkyl groups. Examples include bis
(tallowamidoethyl) ammonium, or bis (stearylamidoethyl) ammonium, mono or di-methosulphates.
Generally speaking tetra alkyl ammonium fabric conditioners such as dimethyl ditallowyl
ammonium chloride are difficult to cream, tending to form coagulated masses which
are difficult to disperse, unless the initial active concentration of the dilute dispersion,
and the electrolyte concentration, are relatively dilute, e.g. from 4 to 8% by weight
and from 0.3% to 0.5% respectively. The creamed concentrates of such quaternary ammonium
salts are correspondingly dilute, compared to amidoamine derivative creams, and therefore
of less commercial value. Mixtures of amido amine derivatives with other quaternary
fabric conditioners in which the former component is present in concentrations of
about 40% or more of the total active weight will generally form acceptable creams
according to the invention.
[0017] For instance we have creamed mixtures of amido imidazolines with ditallowyl, or distearyl,
mon-or di-(lower, e.g. C₁to ₄, alkyl) ammonium salts, such as distearyl dimethyl ammonium
chloride, or with ditallowyl or distearyl benzalkonium or pyridinium salts or with
alkoxylated (e.g. ethoxylated) amido amines or imidazolines, such as a bis (tallowamidoethyl)
mono (1 to 8 mole) polyoxyethylammonium salt or quaternised ammonium salt.
[0018] For all the foregoing fabric conditioners the counter ion is usually chloride, sulphate,
phosphate methosulphate, ethosulphate, or an organic ion such as formate, acetate,
citrate, tartrate, or lactate.
[0019] The C15-22 groups (usually predominantly C16 and/or C18 groups) are preferrably straight
chain or less preferrably branched chain alkyl groups, which may contain a proportion,
preferably minor, of alkenyl groups such as oleyl groups. For maximum softening we
prefer to use hard tallow or other alkyl groups having an iodine number less than
10, preferrably less than 5. However for ease of manufacture the partially unsaturated
feedstocks are more usually selected.
[0020] Preferably, according to our invention, 1 to 20% e.g. 2 to 18%, typically 3 to 16%
of cationic fabric conditioner, based on the total weight of the dispersion, is dispersed
in water. The water preferably has an elevated temperature between 40°C and boiling
e.g. 50 to 80°C. The fabric conditioner is preferably added as a concentrate in a
water miscible organic solvent e.g. a mono-or dihydric alcohol or ether alcohol such
as methanol, ethanol, propanol, isopropanol, ethylene glycol, ethylene glycol mono
methylether, diethylene glycol or diethylene glycol mono methyl ether. The concentrate
preferably has a concentration of greater than 50% e.g. 75 to 95% preferably 90% of
the fabric conditioner based on the weight of the concentrate. Generally the higher
the concentration, the better, consistent with adequate mobility to permit dispersion
in, or mixing with, the aqueous electrolyte.
[0021] The initial concentration of the fabric conditioner in the dispersion is important
to obtain satisfactory creaming and in determining the maximum achievable concentration.
[0022] Typically, where the fabric conditioner comprises an amidoamine derivative we prefer
that the initially prepared aqueous dispersion has a concentration of from 5 to 15%.
the exact concentration will depend on the particular fabric conditioner and the desired
final concentration. If the initial concentration is above a critical maximum (typically
about 17% in the case of amido amine derivatives, or 8% in the case of tetra alkyl
amonium salts) spontaneous creaming may not occur.
However the maximum achievable concentration of the cream is usually about double
the initial concentration. Accordingly we prefer to employ initial concentrations
close to the maximum e.g. 10 to 15% by weight, in the case of amido amine derivatives
or 6 to 8% in the case of tetra alkyl ammonium salts.
[0023] Before or after addition of the fabric conditioner concentrate an electrolyte is
dissolved in the water. The electrolyte may be a water soluble, non-flocculating,
inorganic, alkali metal or ammonium salt which salts surfactants out of solution,
such as lithium, sodium, potassium or ammonium chloride, sulphate, nitrate, acid phosphate,
bromide, iodide, phosphonate, bicarbonate, acid silicate, borate, sulphite or phosphite,
a water soluble alkaline earth metal salt such as calcium chloride or bicarbonate,
or a water soluble alkali metal organic salt which salts surfactants out of solution
such as sodium formate or acetate. The electrolyte should preferably not be strongly
alkaline. Preferably the addition of the electrolyte to the aqueous dispersion results
in pH of less than 10, more preferably less than 9, e.g. less than 8.5. Alkaline electrolytes
such as sodium carbonate, sodium tripolyphosphate, trisodium phosphate or alkaline
silicate tend to flocculate the fabric conditioner.
[0024] The concentration of the electrolyte required to promote creaming depends on the
particular conditioner. In the case of imidazolinium fabric conditioners the concentraton
is preferably between 3 and 15% by weight of the dispersion, more preferably 5 to
12% by weight e.g. 6 to 10%. In the case of tetra alkyl ammonium fabric conditioners
electrolyte concentrations of from 0.3 to 0.5, eg 0.4% are preferred.
[0025] Creaming occurs after a few hours standing and proceeds rapidly until the concentration
has risen to approximately double the initial concentration e.g. usually about 25
to 40% of the fabric conditioner by weight of the cream.
Usually this occurs within 24 hours. The cream is preferably separated from the clear
aqueous phase in which a substantial proportion of the solvent and of the water soluble
organic impurities remain, leaving a purified fabric conditioner. Preferably the cream
has a fabric conditioner content of from 20 to 40% eg 25 to 35% by weight of the cream.
[0026] Creaming may continue at a reduced rate for several weeks, but the cream can easily
be redispersed by gentle stirring or shaking.
[0027] Centrifuging for a short period at 20 to 1,000G preferably 40 to 800G e.g. 50 to
500G may be used to provide a more stable cream more rapidly with reduced tendencies
to undergo further creaming. More vigourous centrifuging e.g. at 20,000G for 2 hours
gives a thick, stable, relatively immobile paste which , however, is readily dispersible
in water. Preferably the centrifugation is effected on material immediately after
mixing. The centrifugation is particularly rapid at elevated temperatures eg 30 to
80°C preferably 50 to 70°C.
[0028] It is possible to prepare compositions, having substantially similar compositions
to the cream, directly by mixing together the aqueous electrolyte and the concentrated
solution of the fabric conditioner in water-miscible organic solvent, in a proportion
adapted to provide the desired final concentration. The term "cream" as used herein
includes such directly formed composition, where the context so permits. The product
differs from that obtained by creaming of a more dilute product in that it normally
contains more solvent, and is less homogeneous, more viscous and less readily dispersible.
Normally the fabric conditioner is added to the electrolyte solution with stirring
until the desired active concentration has been achieved.
[0029] The cream produced may be blended directly with perfumes, colourings, and/or other
minor ingredients such as preservatives, stabilisers, clays such as bentonite and/or
a small amount of the original fabric conditioner concentrate in solvent to stabilise
it or enhance its effectiveness, and sold to the consumer as a high concentration
product, or it may be dispersed in water, before or after addition of any such additives,
to provide more conventional concentrations of the conditioner. The dispersions in
water are generally non-creaming provided the electrolyte concentration is sufficiently
reduced by dilution, e.g. below 3% by weight.
[0030] According to a preferred embodiment of our invention creamed fabric conditioners
may be incorporated in liquid detergents, especially non-ionic based liquid detergents.
[0031] Preferably a softened liquid detergent according to our invention comprises: up to
30% by weight e.g. 5 to 25% by weight, preferably 8 to 20% by weight of surfactant,
which is preferably at least predominantly non-ionic and/or amphoteric surfactant;
and up to 15%, preferably 1 to 10%, by weight of active matter, based on the weight
of the composition, of fabric conditioner cream.
[0032] The detergent may contain sufficient electrolyte to form a solids-supporting structure,
e.g. up to 15% in solution, and preferably includes a builder in an amount up to 40%
by weight e.g. 5 to 30% of zeolite, sodium tripolyphosphate, potassium pyrophosphate,
N.T.A., E.D.T.A. or citrate.
[0033] The structure of our novel fabric conditioner cream can readily be identified with
an optical microscope. Compositions of our invention show a predominantly spherulitic
structure. When the spherulites are observed between crossed polarisers each spherulite
shows evidence of a dark cross, similar to the so called "Maltese Cross" texture which
is a characteristic of a liquid crystal 'G' phase. Electron microscopy suggests a
substructure possibly entailing smaller spherulites agregated in concentric layers
to form larger spherulites.
[0034] Neutron scattering studies on samples prepared in D₂O at 30% active concentration
show two peaks, the first corresponding to a structured feature repeating with a periodicity
of about 50 to 60 Angstrom and the second at about half the periodicity of the first
e.g. 25 to 30 Angstrom. A conventional fabric conditioner e.g. containing only 100
ppm electrolyte gave peaks corresponding to double these periodicities e.g. 100-120
Angstrom and 50 to 60 Angstrom respectively.
[0035] The invention is illustrated by the following examples:
Example 1
[0036] An initial concentrate consisting of a 90% by weight solution of ditallowyl imidazolinium
methosulphate in isopropanol was added to a solution of 5% by weight calcium chloride
in water at 60°C and stirred for 15 minutes to give a 15% by weight active dispersion.
After the dispersion had been allowed to stand for 7 days, a mobile cream was separated
from a clear aqueous phase.
[0037] The cream gave highly effective softening performance compared with a conventional
5% dispersion of the imidazoline in water at equivalent active dosage.
[0038] The cream contained 42.3% by weight total solids (57.7% loss of weight on drying)
and 0.9% by weight isopropanol.
Example 2
[0039] A composition was prepared according to claim 1 but using D₂ O to dilute the initial
concentrates and concentrating to 30% active concentration by adding 7% calcium chloride
and centrifuging. The composition was submitted to neutron scattering which showed
peaks at angles which correspond to regularly repeating structural features at a separation
of 57 and 30 Angstrom respectively.
Comparative Example
[0040] A sample of a non-creamed fabric softener, prepared by diluting the initial concentrate
directly to 30% with D₂O and including conventional levels of electrolyte, i.e. 1000ppm
Ca Cl₂, showed peaks corresponding to periodic features with a spacing of 112 and
56 Angstroms respectively, the product showed no evidence under the optical microscope
of spherulites, was immobile and very difficult to disperse in water at ambient temperature.
Example 3
[0041] A cream type formulation was prepared by adding the initial concentrate directly
to aqueous Ca Cl₂ to provide the same active and electrolyte content as the product
of example 1. The product was more viscous than Example 1, (see table 1) and was less
readily dispersible. It was however substantially more mobile and more readily dispersible
than the comparative example. The product had a slightly non-homogeneous "lumpy" appearance.
Example 4
[0042] Example 1 was repeated with various electrolytes in place of calcium chloride. The
following electrolytes gave compositions which were clearly defined spherulitic compositions
under the optical microscope, and which dispersed rapidly in water:-
(NH₄)₂ SO₄, K₂HPO₄, NaHCO3, (NH₄)₂ SO₃, Na₂ SO₃, K₂SO₄, LiCl, KH₂PO₄, (NH₄) Cl, KCl,
Na₂ SO₄, NaCl, NaHSO₄, KHSO₃.
[0043] The following electrolytes gave compositions which showed evidence of lamellar structure
in addition to spherulites, but which were relatively easily dispersed:-
KBr, Na Br, NaI, NH₄NO₃, Na₂B₄O₇
[0044] The following electrolytes gave compositions which showed evidence of flocculation,
and which were more difficult to disperse:-
K₂CO₃, Na₂ CO₃ Na₅P₃O₁₀, NaSiO₃ (alkaline).
[0045] It was observed that the alkaline electrolytes, with a pH of 9 or greater tended
to cause flocculation. When a flocculated product was prepared in D₂O and examined
by neutron scattering peaks, corresponding to periodicities of 52 and 28 Angstrom
were observed.
Example 5
[0046] A number of samples prepared following the method of example 1, all containing 30%
fabric conditioner and 7.5% CaCl₂, together with the comparative example (made up
in water instead of D₂O) were examined using a "Carrimed" controlled stress rheometer.
[0047] The results were analysed using the Herschel-Bulkley model for the Yield Point and
the Bingham Body Model for the viscosity averaged over the range: 0 to 700 sec.⁻¹
shear and are shown in the table. The results were obtained at 20°C using a cone with
a horizontal angle of 2° and base diameter of 4cm and a plate with a 56.6u gap.
Example 6
[0048] A fabric softener cream was prepared by the method of example 1 using bis(tallowylamidoethyl)
amine hydrochloride as the fabric conditioner. The product was a mobile 30% active
cream which dispersed readily in water and was spherulitic under the optical microscope.
Example 7
[0049] A 6% by weight aqueous dispersion of ditallowyldimethylammonium chloride and 0.4%
CaCl₂ was spherulitic under the microscope, mobile, and readily dispersible in water.
It underwent slow creaming but failed to give a clear separation. For comparison a
15% dispersion containing 7.5% CaCl₂ underwent rapid separation to provide a clear
oil having a concentration of 30% which solidified on cooling, and gave an immobile
waxy slab (see Table 1) which appeared as a fibrous floc under the microscope and
dispersed in water with difficulty. The process was repeated with mixtures of the
ditallowyl dimethylammonium chloride (DDAC) and ditallowylimidazoline methosulphate
(DIM) in various proportions.
[0050] The products showed under the microscope as mixtures of spherulites and floc in substantially
the same relative proportions as the proportion of DIM to DDAC.
[0051] Up to 50% of DDAC the mixtures were mobile and readily dispersible, (see Table 2),
but above 70% DDAC they were immobile pastes.
TABLE I
FABRIC CONDITIONER 30% ACTIVE CREAM |
INITIAL YIELD NM⁻² (H. BULKLEY) |
DYNAMIC YIELD NM⁻² (H. BULKLEY) |
PLASTIC YIELD (BINGHAM) |
PLASTIC VISCOCITY (BINGHAM) |
ditallowylimidazoline methosulphate |
4.77 |
4.044 |
19.66 |
0.184 |
ditallowylimidazoline acetate |
10.44 |
10.08 |
18.56 |
0.1657 |
ditallowylimidazoline methosulphate + 1% bentonite |
- |
- |
12.14 |
0.223 |
ditallowylimidazoline-methosulphate (Ex.3) |
28.35 |
25.38 |
42.99 |
2.112 |
bis(tallowamidoethyl) ammonium methosulphate |
19.68 |
18.88 |
25.70 |
0.6334 |
polyethylene oxy bis-tallow-amidoethyl) ammonium methosulphate |
1.79 |
1.335 |
6.925 |
0.1666 |
ditallowyl(dimethylammonium chloride |
22.98 |
19.21 |
43.31 |
0.896 |
Comparative Example |
- |
- |
71.91 |
4.67 |
TABLE II
WT% DIM |
WT% DDAC |
INITIAL YIELD HERSCHEL BULKLEY |
DYNAMIC YIELD HERSCHEL BULKLEY |
100 |
0 |
4.774 |
4.044 |
90 |
10 |
12.53 |
10.04 |
80 |
20 |
17.9 |
14.23 |
50 |
50 |
22.98 |
18.51 |
1. A composition comprising: water; at least one cationic fabric conditioner having
two C₁₅₋₂₂ alkyl and/or alkenyl groups, dispersed in the water; and dissolved electrolyte
in a concentration sufficient (i) to form said fabric conditioner into an optically
anisotropic spherulitic composition, and/or (ii) to cause creaming if it were present
at said concentration in a more dilute dispersion of said fabric conditioner.
2. A composition formed by dispersing at least one cationic fabric conditioner having
two C₁₅₋₂₂ alkyl and/or alkenyl groups in water in the presence of sufficient electrolyte
to cause creaming thereof, and separating the cream so formed from the rest of the
liquid.
3. A composition according to claim 2 wherein said separation is effected by centrifuging
the dispersion.
4. A composition comprising: water; electrolyte dissolved in said water in a concentration
greater than 1% by weight of said composition; and a cationic fabric conditioner comprising
at least 40% by weight, based on the total active weight, of an amidoamine derivative
having two C₁₅₋₂₂ alkyl and/or alkenyl groups, dispersed in the water as optically
anisotropic spherulites.
5. A composition according to any foregoing claim wherein said fabric conditioner
comprises at least 40% by weight of an amidoamine derivative, based on the total active
weight, and is present in a concentration of from 18 to 50% by weight of said composition.
6. A composition according to claim 5 wherein the concentration of said fabric conditioner
is from 20 to 40% by weight of said composition.
7. A compostion according to claim 6 wherein said fabric conditioner is present in
a concentration of from 25 to 35% by weight of said composition.
8. A composition according to any foregoing claim wherein said fabric conditioner
comprises at least 40% by weight of an amidoamine derivative, based on the total active
weight, and said electrolyte is present in a concentration of from 3 to 15% by weight
of the composition.
9. A composition according to claim 8 wherein said electrolyte is present in a concentration
of from 5 to 12% by weight of said composition.
10. A method of preparing a creamed fabric conditioner which comprises forming a dispersion
of a cationic fabric conditioner in water in the presence of sufficient electrolyte
to effect creaming of the fabric conditioner, and separating the cream so formed.
11. A method according to claim 10 wherein said dispersion initally contains from
2 to 18% by weight, based on the total weight of the dispersion of a fabric conditioner
comprising at least 40%, based on the total active weight, of an amidoamine derivative.
12. A method according to claim 11 wherein the electrolyte is present in a concentration
of from 3 to 15% by weight of said dispersion.
13. A method according to any of claims 10 to 12 wherein said separation is effected
by centrifuging.
14. A method of preparing a concentrated fabric conditioner which comprises mixing
together: a cationic fabric conditioner comprising at least 40%, based on the total
active weight, of an amidoamine derivative; water; and electrolyte; in proportions
adapted to provided a concentration of from 18 to 50% by weight, based on the total
weight of the composition, of said fabric conditioner and from 1 to 15% based on the
total weight of the composition of said electrolyte.
15. A liquid detergent comprising water, from 5 to 25% by weight of nonionic and/or
amphoteric surfactant and a composition according to any of claims 1 to 9, added in
a proportion of from 1 to 10% expressed as weight of active matter based on the total
weight of the detergent.
16. A composition according to claim 14 containing from 5 to 30% by weight of a builder.
17. A composition according to any of claims 1 to 10 substantially as described herein
with reference to any one of the examples.