Technical field
[0001] This present invention deals with concentrated aqueous dispersions or emulsions of
insoluble cationic compounds, used as fabric softeners, with an improved stability
with time, and in regards to temperature variations in relation to the viscosity and
dispersibility in water of the said dispersons. It also deals with the adequate preparation
methods for the obtention of the said dispersions.
State of the former technique
[0002] The appearance, in the last years, of more concentrated liquid fabric softener compositions
is undoubtedly due to economical motivations, and to a greater convenience to the
consumer. This fact has originated the emergence of serious technical problems related
with the increase in active matter, fundamentally insoluble cationic compounds, from
concentrations ranging between a 3% to a 7% in the traditional diluted compositions,
to proportions higher than 10% in the currently called concentrated softeners. The
primary problems have to do with the physical properties of the concentrated compositions,
essentially with their viscosity and dispersibility in water and with the variation,
in negative sense, of the said properties with temperature and time of storage, as
well as with relatively abrupt changes of temperature.
[0003] It has been known for a time, for instance in US-Patent No. 3,681,241, that the addition
of small quantities of such electrolytes as salts of divalent metals causes a considerable
decrease in viscosity. In German Patent No. 29 11 198 there has also been a description
of the use of aluminium salts, producing an anti-gelling effect. But these solutions
are only partly effective, as the quantity of electrolyte that can possibly be added
has to be very small, otherwise there could be problems caused by the formation of
clots and rupture of phases. Another attempt to solve this problem consists in substituting
soluble cationic products instead of the insoluble cationic products, as described,
for instance, in the European Patent Application No.00 406, but these compositions
do not give the required softening performance, as it is necessary for the cationic
compound to become bound to the surface of the fabric for the softening effect to
occur, and these compounds, because of their solubility in water, are dragged away
in a great proportion during the rinsing process. The European Patent Applications
Nos. 13 780 and 18 039 describe the use of non-cyclic hydrocarbons, fatty acids or
their esters, and fatty alcohols as additives to decrease viscosity and to enhance
the stability of concentrated softening compositions, but the effectivity of these
coumpounds decreases noticeably with low storage temperatures, so the solution provided
by them is only a partial one. The addition of non-ionic alkoxylated surfactants is
knows for diluted compositions, and has been applied in concentrated compositions,
for instance in the German Patent No. 29 11 198, in the French Patent No. 2 482 636
and in the US-Patent No. 3,947,076, although its utilization has not been sufficiently
specified as far as the types of products are concerned, nor as to the effect produced
therewith, and, nevertheless, their stabilizing action on viscosity has little effectivity
at high temperatures, so it also has to be considered as only a partial answer.
[0004] The utilization of alkoxylated amines in softener composition has been known now
for some time, as shown in the following documents: US-Patent No. 3,850,818, German
Patent Application No. 16 19 043, US-Patent No. 4,076,632, US-Patent No. 4,157,307,
European Patent Application No. 21 476, US
-Patent No. 4,320,013. The part played by the alkoxylated amines in the compositions
described by the documents above cited are both of fabric softening and of enhancing
the stability of the dispersion, but all of them are referred to diluted softener
compositions, and, moreover, the stabilizing action of the alkoxylated amine has to
be concurrent with the joint action of other additives, like urea or alcohols. In
European Patent Application No. 56 695 is introduced for the first time the concept
of the action of alkoxylated amines as factors to achieve a proper viscosity, as well
as a satisfactory stability, in concentrated softener compositions, provided that
it is associated to the addition of low levels of electrolyte. Nevertheless, there
is a serious limitation, as it is stated that the number of mols of oxyalkyl which
conform the two alkoxylated substituents of the amine cannot ever be higher than 14
and that preferably it has to be between 2 and 8, as otherwise it should be necessary,
to maintain the adequate viscosity, to significantly increase the presence of electrolyte,
which would be deleterious to product stability. This limitation reduces the range
of what is possible in the technique of obtention of stable concentrated softener
compositions, and does not allow the utilization of alkoxylated amines with a high
degree of alkoxylation which, moreover, are significantly lower in cost than those
of a lower degree of alkoxylation.
Vindication of the invention
[0005] The invention herein solves these problems, as in a surprising way unexpected results
are achieved in good characteristics of viscosity and a good dispersibility in water
of concentrated aqueous dispersions of insoluble cationic compounds, as well as an
extended stabilization thereof in ranges of temperatures between 0° and 50
*C, by means of the addition of amines with a high degree of alkoxylation in union
with a precise and definite system of two non-ionic components. Also, surprisingly,
the dispersions described in the invention herein exhibit an excellent adaptability
in the maintenance of their physical properties versus abrupt and wide changes of
temperature. Also inherent difficulties to the process of obention of aqueous concentrated
dispersions of cationic softeners are solved.
[0006] The fundamental object of the invention herein, then, is to achieve concentrated
aqueous dispersions of insoluble cationic softeners with adequate viscosity and dispersibility
and an improved stability in storage and in abrupt temperature changes. Another aim
of the invention is the achievement of more economically profitable concentrated softener
compositions. Another aim of the invention herein is to develop a process to obtain
the compositions hereof, easy and dependable in its results.
Description of the invention
[0007] The invention herein relates to fabric softener compositions which are basically
constituted by the following components:
1. From 10% to 20% by weight of a cationic water-insoluble softener compound, or of
a mixture of the such.
2. From 0,1% to 3% by weight of an alkoxylated tertiary amine, or of its correspondent
ammonium salt, having the general formula:

wherein R1 represents an alkyl or alkenyl group, between 10 to 20 carbon atoms, n is an integer
between 1 and 4; x and y represent numbers between 10 and 50, so that the sum thereof
be between 20 and 100 (x + y = 20 to 100).
3. 0,5% to 5% by weight of a mixture of two non-ionic surfactants pertaining to the
groups:
A) C10 to C20 alkoxylated fatty alcohols or C7 to C10 alkoxylated alkylphenols with a number of mols of alkylene oxide between 25 and 75
per mol of alcohol or phenol.
B) C10 to C20 alkoxylated fatty alcohols or C7 to C10 alkoxylated alkylphenols with a number of alkylene oxide mols between 1 and 5, per
mol of alcohol or phenol in such a way that the ration between A and B ranges between
10:1 and 1:10.
[0008] The above mentioned compounds are dispersed or dissolved in water with a pH ranging
between 3 and 5.
[0009] It is highly preferred, in the composition of the invention herein, to add small
quantities of an electrolyte, preferably salts of strong acids and divalent metals,
the effect of which is very beneficial on the viscosity parameter. The most adequate
proportions of the said electrolyte range between 0.02% and 0.15%. Below the inferior
limit, the electrolyte action is very unsubstantial, and above the upper limit, there
is risk that undesirable phenomena may appear, undermining the stability of the compositions,
due to problems of phase disruption.
[0010] The insoluble cationic compounds of the invention herein belong to the type usually
used in aqueous dispersions with softening activities on textile fabrics, preferably
those belonging to the following groups:
1 - Salts of quaternary ammonium with two long chain alk(en)yl groups, C10 to C20.
2 - Imidazolinium quaternary salts, with two long chain alk(en)yl groups C10 to C20'
and are incorporated into the compositions in a proportion ranging between a 10% to
a 20% by weight of the aforesaid composition, and in a preferred proportion of 11%
to a 16% to achieve an optimal ratio of softener activity/viscosity.
[0011] The alkoxylated tertiary amines with a number of mols of alkylene oxide higher than
20 per mol of amine, are highly important to achieve a viscosity between 50 and 900
centipoises with a good stability, during long storage terms. In contradistinction
to what was anticipated in the previous technique as expressed in the European Patent
No. 56 695, it has been possible to adjust the formula in a surprising way so as to
make it feasible that highly alkoxylated amines perform the said function with the
presence of small quantities of electrolyte in a range of 500 to 1000 ppm. Notwithstanding
the fact that the said amines can be used in proportions ranging from 0.1% to 3% by
weight, the preferred proportions are those from 0.5% to 1.5%, with a view to achieve
a good balance between the desired effect of viscosity reduction and the incidence
in the final cost of the composition.
[0012] The system of non-ionic surfactants herein shows itself to be effective to achieve
compatibility of the alkoxylated amine with a high degree of alkoxylation with the
formulation in presence of small amounts of electrolyte, and it is also basic to confer
on the dispersion its qualities of elasticity versus temperature changes during storage.
These non-ionic surfactants are selected from amongst the group of alkoxylated fatty
alcohols or alkoxylated alkylphenols with a general formula:

wherein R
2 represents an alk(en)ylic group between C
s and C
20 or phenylalkyl from C
7 to C
10, n is an integer from 1 to 4, and z is a number between 1 and 75.
[0013] For a good execution of the invention, it is necessary to use two non-ionic surfactants
which are clearly differentiated on their z value:
A) A non-ionic surfactant according to the general formula II, in which z ranges between
25 and 75.
B) A non-ionic surfactant according to the general formula II, in which z ranges between
1 and 5.
[0014] Although the proportion between A and B can have a range between 10:1 to 1:10, the
preferable proportion is between a range of 3:1 to 1:3.
[0015] The process of obtention has also a great importance to obtain good results in viscosity,
dispersibility in water, and stability. The temperature during the said process has
to be maintained with decreasing rhythm between 60°C and 30°C, but the most important
factor is the order and rate of addition of the different components. So, for example,
it is convenient to add to the water, in the first place, a molten mixture of the
alkoxylated amine together with the system of non-ionic surfactants, and to adjust
the pH by means of a strong acid between 3 and 5. The addition of the insoluble cationic
compound is performed in a fractionated way, alternating with additions, also in a
fractioned way, of the electrolyte. Small variations in the order of addition are
the cause of dispersions with a very high initial viscosity or with a bad performance
versus temperature variations.
[0016] The characteristics of the dispersions so obtained are as follows:
- pH = 3 to 5
- Specific Gravity = 0.95 to 1.05 g/cc
- Initial Viscosity = 50 to 400 cps
- Viscosity after 8 weeks at room temperature = 50 to 400 cps.
- Viscosity after 2 weeks at 0°C to 5°C: Less than 900 cps.
- Viscosity after 2 weeks at 45°C: Less than 900 cps.
- Dispersibility in water: Excellent,
being these characteristics very appropriated from the viewpoint of its storage and
of its use as a fabric liquid softener composition.
[0017] The detailed description of the different components of the invention herein are
described below.
[0018] The insoluble cationic compounds are the active softening matter, and can be selected
from amongst the following groups:
1. Quaternary acyclic ammonium salts represented by the general formula:

wherein R3 and R4 represent alkyl or alkenyl groups of from 10 to 20 carbon atoms, R5 and R6 represent short alkyl groups from 1 to 4 carbon atoms, and A represents the salt
counteranion, as, for example, halides or methyl sulphate. These are very widely known
products and, as examples, the following could be quoted: ditallow dimethyl ammonium
chloride; dicoco dimethyl ammonium chloride; distearyl dimethyl ammonium chloride;
di(hydrogenated-tallow) dimethyl ammonium methyl sulfate; di(hydrogenated tallow)
dimethyl ammonium chloride; ditallow dimethyl ammonium methyl sulfate. They are easily
available in the market under different trademarks, like AdogenR, VarisoftR (Sherex Chemicals), QuartaminR (Kao Corp.), ArquadR (Akzo), PräpagenR (Hoechst, etc... Of these, di(hidrogenated tallow) dimethyl ammonium chloride is
preferred.
2. Quaternary imidazolinium salts represented by the general formulae:

where R71 R8, R9 and R10 represent saturated or unsaturated alkyl groups, with 10 to 20 carbon atoms, and
A represents the salt counteranion of a mono- protic acid, such as, for example, halide
or methyl sulfate. This type of products is also well known, and as examples the following
are quoted: Methyl-1-(hydrogenated tallow) amido ethyl-2-(hydrogenated tallow) imidazolinium
methyl sulfate; methyl-1-tallow amido ethyl-2 tallow imidazolinium methyl sulfate;
methyl-1-oleyl amido ethyl-2-oleyl imidazolinium chloride; 1-ethylene bis(2-tallow,
1-methyl imidazolinium methyl sulfate). Preferred compounds are methyl-1-(hydrogenated
tallow) amido ethyl-2-(hydrogenated tallow) imidazolinium methyl sulfate, marketed
by Sherex Chemical Company under the designation VarisoftR445, and 3-methylethyl-1-(hydrogenated
tallow) amido ethyl-2-(hydrogenated tallow) imidazolinium methyl sulfate, marketed
by Rewo Chemische under the designation RewoguatR W7500H.
[0019] The alkoxylated amines have the general formula I, wherein R
1 represents an alkyl group, saturated or non-saturated, from 10 to 20 carbon atoms,
as those corresponding to coconut, oleic, tallow, hydrogenated tallow, and hydrogenated
tallow is preferred; n is an integer between 1 and 4, value 2 being preferred, which
corresponds to ethoxylated amines. The values of x and y range between 10 and 50 in
such a way that the total sum thereof ranges between 20 and 100, this is to say, the
number of mols of ethylene oxide per amine mol must range between 20 and 100, although
the preferred values of x + y range between 20 and 50. This type of products is available
in the market under various commercial designations as, for example, Etilenox
R (Pulcra),
Ethomeen
R (Akzo), Genamin
R (Hoechst). Highly preferred are the amines of hydrogenated tallow with 20 mols of
ethylene oxide such as Etilenox
R KM-30 of Pulcra, S.A. and Genamin
R S-250 of Hoechst A.G., and with 50 mols of ethylene oxide as, for example, Ethomeen
R HT60 of AKZO Chemie.
[0020] Non-ionic surfactants have the general formula II, wherein R
2 represents an alkyl group of between 8 and 20 carbon atoms like, for example, those
corresponding to fatty alcohols like lauric, miristic, palmitic or stearic alcohols,
or the mixtures thereof, or an alkyl phenyl group with 7 to 10 carbons, as those corresponding
to the alkyl phenols with 8 and 9 carbon atoms. The preferred groups are those corresponding
to the lauric alcohol and nonylphenol. The value of n can be between 1 and 4, being
the preferred value that of 2, and, therefore, the ethoxylated products. According
to the invention herein, a binary system of non-ionic oxyethylenated surfactants is
necessary in function of the Z value:
A) A non-ionic surfactant according to general formula II and with a Z value between
25 and 75, the preferred values being between 25 and 50.
B) A non-ionic surfactant according to the general formula II with a Z value between
1 and 5, preferably between 1 and 3.
in a weight ratio in the range from 10:1 to 1:10, the preferred weight ratio being
that of between 3:1 and 1:3. These products are well available in the market and can
be found under the following commercial designations: Dobanol R (ICI),
Dowfax
R (
Dow Chemical), Emulgen
R (Kao Corp.), Catinex
R (Pulcra, S.A.), etc...Especially preferred is the binary system nonylphenol with
30 mols of ethylene oxide together with nonylphenol with 1.5 mols of ethylene oxide,
with a weight ratio ranging from 3:1 to 1:3.
[0021] Besides the essential components, a series of optional additives can be incorporated
to the compositions of the invention herein which are conventionally used in the field
of fabric softeners, like dyes, perfumes, supplementary viscosity modifiers, emulgents,
optical brighteners, antioxidants, germicides, fungicides, moisteners, etc...
[0022] It is especially indicated, for a better viscosity control, the use of electrolytes,
as salts of divalent metals with strong acids, in weight ratios ranging between 200
and 1.500 ppm. Especially preferred electrolytes are calcium chloride and magnesium
sulfate.
[0023] Other optional additives, which are indicated as auxiliary in viscosity control,
are lineal or ramified short chain alcohols from 1 to 4 carbon atoms. Isopropilic
alcohols, paticularly, may be had in a proportion, between a 1% and a 4%, but not
in a bigger proportion that may cause lack of stability.
[0024] Optional components indicated to improve the water absorbancy of the fabrics treated
with the softeners are the emulsified silicones, such as DC-347, DC-346 and DC-HV490,
marketed by Dow Corning. Small amounts, of an order of a 0.01% to a 0.3% in active
matter, are employed.
[0025] Optical brighteners can also be employed, like, for example, derivatives of estilbene
and distirylbiphenyl, marketed by Ciba-Geigy as
Tinopal
R.
[0026] It is convenient here to remark that, in what concerns the more detailed aspects
of the process of obtention given by the invention herein, that the said process exhibits
two very distinct phases:
A - The addition of a molten mixture of the non-ionic components and the alkoxylated
amine on water, with stirring, at a temperature between 50° and 60°C, and the addition
of a strong acid up to a pH between 3 and 5.
B - Addition of the molten cationic component in two fractions of the 70% and 30%,
respectively, of the total amount, alternating with the addition of electrolyte, also
in two fractions corresponding to a 30% and a 70% of the total quantity of the same,
in such a way that after the first addition, of the 70% of the cationic compound,
follows the 30% of the electrolyte, and that, following a time of stirring and mixing,
the second fraction of a 30% of the cationic component is added and, upon this, the
remaining 70% of electrolyte. All this part of the process takes place with stirring
and at a temperature between 45° and 55°C.
[0027] Once the dispersion has taken place in the manner hereinabove, it is left to cool
to 30° to 40°C, adjusting the pH again between 3 and 5, and the remaining optional
ingredients can now be added.
[0028] It is important to remark that the order of addition hereinbefore is essentiel to
achieve dispersions with the desired viscosity and stability.
[0029] For a better understanding of the description of the invention given herein, the
following examples are given, with the statement that they must not be construed as
restrictions to the aforesaid invention:
Example I
[0030] 1.5 parts of etoxylated hydrogenated tallow amine with 25 mols of ethylene oxide
per mol of amine are mixed, at a temperature of 55°C, together with 1 part of etoxylated
nonylphenol with 30 mols of ethylene oxide per mol of nonylphenol and 1 part of etoxylated
nonylphenol with 1.5 mols of ethylene oxide per mol of nonylphenol. The said molten
mixture is added upon 70 parts of deionized water, at a temperature of 50° to 60°C,
and with strong stirring. Hydrochloric acid 1 N is added until a pH of 3 to 4 is reached.
Upon this, and keeping a temperature between 50° and 55°C, and a strong stirring,
11.7 parts of molten di(hydrogenated tallow) dimethyl ammonium chloride are added,
with an active matter content of a 75%, and after this 0.03 parts of calcium chloride
are added, in 10% aqueous solution. The mixture is stirred for 5 minutes, and then
5.0 more parts of molten cationic component are added and 0.07 parts of calcium chloride.
The dispersion is cooled to 40°C in 10 minutes, maintaining the stirring on, and 0.6
parts of DC-HV490 are added (a 35% silicone emulsion marketed by Dow Corning). It
is left to cool to 30° to 35°C, and other optional ingredients are added, as desired,
such as perfume, dyes, etc... and deionized water is added to make up 100 parts. The
dispersion is cooled to 25°C, and pH is brought to between 3.5 and 4.5 and, after
this, the product is bottled.
[0031] With the dispersion prepared as hereinbefore, the following tests and measurements
are performed:
Initial Viscosity. - The dispersion is left to settle until the day following its
preparation, and its viscosity is measured at 20°C with a Brookfield LV Viscosimeter.
Initial viscosity for the solution thus prepared is 200 centipoises.
[0032] Stability at room temperature. - The dispersion, well packed and closed, is stored
at a temperature of 25°C ± 5°C for two months, and at the end of this period a viscosity
measurement is performed at 20°C. The viscosity value observed for the dispersion
thus prepared is 210 centipoises.
[0033] Stability at high temperatures. - A sufficient amount of sample of the dispersion
is hermetically sealed in the same vessel where the viscosity value is to be determined,
and it is kept in a stove at 45°C during five days. Then, the sample is removed from
the stove, left for another day at room temperature, and its viscosity is measured
at 20°C. The sample is again hermetically sealed and it is again-placed in the stove
at 45°C, and it is again removed at the end of that period, it is left to stabilize
during another day at room temperature and its viscosity is measured at 20°C. The
values that have been found are:
Viscosity after 5 days = 380 centipoises
Viscosity after 10 days = 850 centipoises.
[0034] Stability at low temperatures. - A sample of the dispersion is hermetically sealed
in the same vessel where the viscosity is to be tested, and it is placed in a refrigerator
at 3°C ― 2°C. The sample is removed after five days, it is left for another day at
room temperature and its viscosity is tested at 20°C.
[0035] The sample is again placed in the refrigerator, for another four days, and then it
is removed, left to stabilize for one day at room temperature, and then the viscosity
is tested at 20°C. The values of viscosity that have been found are:
Viscosity at 5 days = 425 centipoises
Viscosity at 10 days = 800 centipoises
Elasticity versus temperature. - A sample of the dispersion is taken, and placed
in an appropriate vessel, it is placed in a bath provided with a temperature regulator,
and the temperature is adjusted at 20°C and the viscosity is then measured. It is
heated to 70°C in 30 minutes, and the viscosity is again measured. It is cooled again
to 20°C in 30 minutes, and the viscosity is tested. The values found are:
Viscosity at 20°C = 200 centipoises
Viscosity at 70°C = 490 centipoises
Viscosity at 20°C = 325 centipoises
[0036] Dispersibility in water. - This test is approximate and orientative. A graduate cylinder
is filled with a liter of water at 20°C ± 5°C of temperature, and with a hardness
of 20°HF. 30 grams of the dispersion, which has been kept two months stored at a temperature
of 20°C ± 5°C, are poured on the surface from a height of 8 cm. That part of the dispersion
which results not dispersed in the water remains in a ring shape in the higher or
lower part of the graduated cylinder, according to its density, and an arbitrary scale
is assigned to it, from 0 to 10. 0 means total dispersion and 10 no dispersion. The
volume of water to which the dispersion has not arrived is measured, so that the optimal
volume is that of 0 ml, and the worst one is that of 1000 ml.
[0037] By means of these data, an approximated and arbitrary scale is made, as follows:

[0038] Applying these criteria to the dispersion obtained by the invention herein, its dispersibility
in water is excellent.
Example II
[0039] Performing the same operations as decribed under example I, a dispersion is prepared
with the following ingredients:
[0040]

The dispersion exhibits the following characteristics, determined according to the
criteria established in
example I:
[0041]

Example III
[0042] Performing the same operations as described herein under example I, a dispersion
is prepared with the following ingredients:

[0043] The dispersion exhibits the following characteristics, determined according to the
criteria established in
example I:
[0044]

Example IV
[0045] Performing the same operation as described herein under example I, a dispersion is
prepared with the following ingredients:

The dispersion exhibits the following characteristics, determined according to the
criteria established in
example I:
[0046]

The dispersions described in the examples I to IV exhibit excellent viscosity, dispersibility
and stability characteristics during storage and in extreme temperature conditions
for their use as fabric concentrated softeners.
Exameles V to XIV
[0047] It is the purpose in the following examples to show the importance of the amine with
a high degree of alkoxylation, and of the system of non-ionic surfactants in the viscosity,
dispersibility in water, and stability of the dispersions. To the end of the establishment
of comparative criteria, some basic aspects, such as the contents in active insoluble
cationic matter, nature and contents of the alkoxylated amine, and total contents
in non-ionic surfactant, have been harmonized.
[0048] The abbreviation to design the different ingredients are as follows:
DHTDMAC: Di(hydrogenated tallow) dimethyl ammonium chloride
DTIMS-3M: 3-methyl-1-tallow amido ethyl-2 tallow imidazolinium methyl sulfate
HTA 25: Hydrogenated tallow amine with 25 mols of Ethylene oxide
NP 30: Nonyl phenol with 30 mols of Ethylene oxide
NP 14: Nonyl phenol with 14 mols of Ethylene oxide NP 9: Nonyl-phenol with 9 mols
of Ethylene oxide
NP 1,5: Nonyl phenol with 1.5 mols of Ethelene oxide LA 50: Lauric alcohol with 50
mols of Ethylene oxide
LA 2,7: Lauric alcohol with 2.7 mols of Ethylene oxide
TweenR60: Polyoxyethylene sorbitane monostearate (ICI)
GLYC (OP-OE): Glycerine with 8 mols of Ethylene oxide and 28 mols of propylene oxide
Plurafac R40: Polyalkoxylated alcohol, from 13 to 15 carbon atoms, marketed by Ugine Kuhlmann
[0049] In Table 1 are shown the different compositions prepared following the basic ideas
as described in example I, and in Table 2 their characteristics are detailed according
to the criteria given in example I.
[0050] On checking the data in Tables 1 and 2, it can be inferred that the addition of the
highly alkoxylated amine causes an improvement in the stability of the compositions
at room temperature and an improvement in the dispersibility of the compositions in
water. The incorporation of non-ionics improves the stability at low temperatures,
but it is not effective at high temperatures. All dispersions with a system of non-ionics
as described in the invention herein cause an improvement of stability both at low
and at high temperatures, and cause the viscosity value at room temperature to stay
practically unchangeable, and give an excellent dispersibility in water.

1. Fabric concentrated softener compositions with a good viscosity and dispersibility
in water and an improved stability versus a long period of storage, and versus temperature
changes, its essentiel components being as follows:
A. 10 to 20% by weight of a water-insoluble cationic fabric softener compound, or
a mixture thereof.
B. 0.1 to 3% by weight of a tertiary alkoxylated amine or its corresponding ammonium
salt, with a general formula as follows:

wherein R1 represents an alkyl or alkenyl group, with 10 to 20 carbon atoms, n is an integer
from 1 to 4, and x and y represent numbers between 10 and 50, being the total sum
of both between 20 and 100. (x + y = 20 to 100)
C. 0.5 to 5 % by weight of a mixture of two non-ionic surfactants belonging to the
following groups:
i.- C8 to C20 alkoxylated fatty alcohols or C7 to C10 alkoxylated alkyl phenols, with a number of mols of alkylene oxide per mol of alcohol
or phenol ranging between 25 and 75.
ii.- Cs to C20 alkoxylated fatty alcohols or C7 to C10 alkoxylated alkyl phenols with a number of mols of alkylene oxide ranging between
1 and 5,
in such a way that the weight proportion of the said mixture of non-ionic surfactants
is in the range from 10:1 to 1:10.The said ingredients dissolved or dispersed in water at a pH ranging between 3 and
5.
2. Compositions according to claim 1 characterized in that the water-insoluble cationic
component or components are selected from amongst the following groups:
A.-Non-cyclical quaternary ammonium salts having the general formula

wherein R3 and R4 represent C10 to C20 alkyl or alkenyl groups, R5 and R6 respresent short chain C1 to C4 alkyl groups and A represents the salt counteranion from a strong acid
B.-Quaternary imidazolinium salts having the following general formulae:

where R7, R8, R9 and R10 represent saturated or unsaturated alkyl groups, with chains from 10 to 20 carbon
atoms, and A represents the counteranion of a strong acid.
3. Compositions according to claims 1 and 2, wherein the water-insoluble cationic
component or components are: Di(hydrogenated tallow) dimethyl ammonium chloride and/or
3-methyl-1-(hydrogenated tallow) amido ethyl-2-(hydrogenated tallow) imidazolinium
methyl sulfate.
4. Compositions according to claims 1 to 3, characterized in that the tertiary alkoxylated
amine is: Ethoxylated (hydrogenated tallow) amine with 25 mols of ethylene oxide or
ethoxylated (hydrogenated tallow) amine with 50 mols of ethylene oxide.
5. Compositions according to claims 1 to 4, characterized in that the highly alkoxylated
non-ionic surfactant component is selected from amongst ethoxylated nonyl phenol with
30 mols of ethylene oxide or ethoxylated lauric alcohol with 50 mols of ethylene oxide
and the non-ionic surfactant with a low level of alkoxylation is selected from amongst
ethoxylated nonyl phenol with 1.5 mols of ethylene oxide or ethoxylated lauric alcohol
with 2.7 mols of ethylene oxide.
6. Compositions according to any preceding claim, characterized in that an electrolyte
is added to them as an agent to improve the value of viscosity, belonging to the salts
of divalent metals with strong acids, with a weight ratio ranging between 0.02% and
0.15% of the total weight of the composition.
7. Compositions according to any preceding claim, characterized by having the following
components:
A.- 12 to 16% by weight of a water-insoluble cationic softener compound or a mixture
thereof.
B.- 0.5 to 1.5% by weight of an alkoxylated tertiary amine having the general formula
I, with 20 to 100 mols of alkylene oxide per mol of amine.
C.- 1 to 3% by weight of a mixture of two non-ionic surfactants pertaining to the
following groups:
i.- C8 to C20 alkoxylated fatty alcohols or C7 to C10 alkoxylated alkyl phenols with a number of mols of alkylene oxide ranging from 25
to 75 per mol of alcohol or phenol.
ii.- C8 to C20 alkoxylated fatty alcohols or C7 to C10 alkoxylated alkyl phenols with a number of alkylene oxide mols ranging from 1 to
5 per mol of alcohol or phenol
wherein the weight ratio between the two non-ionic surfactants is in the range from
3:1 to 1:3.
D.-0.03 to 0.15% by weight of an electrolyte, belonging to the type of salts of divalent
metals with strong acids.
The said ingredients dissolved or dispersed in water at a pH ranging between 3.5 and
4.5.
8. A method of making the compositions according to any preceding claim, characterized
in that in a first stage a molten mixture of the non-ionic components is added with
stirring together with the alkoxylated amine on deionized water, in a second stage
a fractioned addition of the water-insoluble cationic compound is effected, alternating
with fractioned additions of electrolyte, all this with stirring, and the preparation
of the composition being finished with the addition of optional ingredients.
9. A method according to claim 8, characterized in that it takes place in a range
of temperatures between 60°C and 30°C.
10. A method according to claims 8 and 9, characterized by the addition of the water-insoluble
cationic compound in two fractions, the first of them being of a 70% of the total
amount and the second to the 30% of the said total amount, alternating with the addition
of the electrolyte also in two fractions, the first being of a 30% of the total amount,
and the second of a 70% of the total amount.