[0001] The present invention relates to the use as a fabric damage inhibitor or fibre protector
of a fabric softening composition comprising a biodegradable quaternary ammonium material.
[0002] Rinse added fabric softening compositions are well known. Typically such compositions
contain a water insoluble quaternary ammonium fabric softening material dispersed
in water at a level of quaternary ammonium material up to 7% by weight in which case
the compositions are considered dilute, or at levels from 7% to 50% in which case
the compositions are considered concentrates. In addition to softening, fabric softening
compositions desirably have other benefits. Such other benefits are particularly important
for consumers who believe that the use of fabric softening compositions causes damage
to the environment and that the damage outweighs the softening benefit obtained.
[0003] A typical wash will include some fabric containing cotton fibres. Abrasion of cotton
fibres under wet conditions results in cotton fibre fibrillation whereby the cotton
fibres are gradually broken down into their component fibrils and into fibrillar sheets.
Such fibrillation is an important mechanism by which fabrics are damaged during wash
processes. Damaged fabrics scatter light to a greater extent than undamaged fabrics
and the scattering causes dulling of fabric colours. Ultimately the damage will result
in mechanical disintegration of the fibre and the consequent failure of cotton garments.
The main causes of fibrillation have been found to be swelling of the fibres when
wet and friction. Both wet and dry friction cause damage.
[0004] It is an object of the present invention to provide a method of inhibiting damage
to cotton fibres and thereby to increase the life of garments containing the fibres.
[0005] According to the invention there is provided the use as a fabric damage inhibitor
or reducer of a fabric softening composition comprising a quaternary ammonium material
having two C₁₂₋₂₈ alkyl or alkenyl groups connected via an ester link to the quaternary
nitrogen atom.
[0006] Throughout this specification the term inhibitor includes a component which confers
protective care or protection on a fibre. In particular it encompasses those materials
which reduce the damage to the fibre which would otherwise occur during the course
of wearing and washing a garment.
[0007] Preferably the composition is a liquid comprising an aqueous base.
[0008] A preferred type of ester-linked quaternary ammonium material for use in the compositions
according to the invention is represented by the formula:

wherein each R₁ group is independently selected from C₁₋₄ alkyl, alkenyl or hydroxyalkyl
groups; and wherein each R₂ group is independently selected from C₈₋₂₈ alkyl or alkenyl
groups; and n is an integer from 0 to 5.
[0009] Preferred materials of this class and their method of preparation are, for example,
described in US 4 137 180 (Lever Brothers). Preferably these materials comprise small
amounts of the corresponding monoester as described in US 4 137 180 for example 1-tallowoxy2-hydroxytrimethyl
ammonium propane chloride.
[0010] Preferably the level of ester linked quaternary ammonium compound is at least 1%
by weight of the composition, more preferably more than 3% by weight of the composition;
especially interesting are concentrated compositions which comprise more than 7% of
ester-linked quaternary ammonium compound. The level of ester-linked quaternary ammonium
compound is preferably is between 1% and 80% by weight, more preferably 3% to 50%,
most preferably 8% to 50%.
[0011] The softening composition may be stabilised at low temperatures by the addition of
nonionic stabilisers. Suitable nonionic stabilisers which can be used include the
condensation products of C₈ - C₂₂ primary linear alcohols with 10 to 20 moles of ethylene
oxide. The alcohols may be saturated or unsaturated. In particular Genapol T-110,
Genapol T-150, Genapol T-200, Genapol C-200 all ex Hoeschst AG, Lutensol AT18 ex BASF,
Genapol 0-100 and Genapol 0-150 ex Hoechst, or fatty alcohols for example Laurex CS,
ex Albright and Wilson or Adol 340 ex Sherex. Preferably the nonionic stabiliser has
an HLB of between 10 and 20, more preferably between 12 and 20.
[0012] Preferably, the level of nonionic stabiliser is within the range from 0.1 to 10%
by weight, more preferably from 0.5 to 5% by weight, most preferably from 1 to 4%
by weight. The mole ratio of the quaternary ammonium compound to the nonionic stabilising
agent is within the range from 40:1 to about 1:1, preferably within the range from
18:1 to about 3:1.
[0013] The composition can also contain fatty acids for example C₈ - C₂₄ alkyl or alkenyl
monocarboxylic acids or polymers thereof. Preferably saturated fatty acids are used,
in particular, hardened tallow C₁₆-C₁₈ fatty acids. Preferably the fatty acid is non-saponified,
more preferably the fatty acid is free; for example oleic acid, lauric acid or tallow
fatty acid.
[0014] The level of fatty acid material is preferably more than 0.1% by weight, more preferably
more than 0.2% by weight. Especially preferred are concentrates comprising from 0.5
to 20% by weight of fatty acid, more preferably 1% to 10% by weight. The weight ratio
of quaternary ammonium material to fatty acid material is preferably from 10:1 to
1:10.
[0015] The compositions of the invention preferably have a pH of more than 2, more preferably
between 2 and 5.
[0016] The composition can also contain one or more optional ingredients, selected from
non-aqueous solvents, pH buffering agents, perfumes, perfume carriers, fluorescers,
colorants, hydrotropes, anti-foaming agents, anti-redeposition agents, enzymes, freeze-thaw
stabilisers, optical brightening agents, opacifiers, anti-shrinking agents, anti-wrinkle
agents, anti-spotting agents, germicides, fungicides, anti-oxidants, anti-corrosion
agents, drape imparting agents, antistatic agents and ironing aids.
[0017] The composition may also contain nonionic fabric softening agents such as lanolin
and derivatives thereof.
[0018] The invention will now be illustrated by the following non-limiting examples and
with reference to the accompanying drawing which is a diagrammatic representation
of the fibre damage test apparatus used. In the examples all percentages are expressed
by weight.
[0019] The figure shows a yarn on yarn abrasion tester with a test yarn 1 comprising fibres.
The two ends of the yarn are attached to metal links 2 and 3. Metal link 2 joins the
yarn to a cord 4 which passes over a first upper yarn guide pulley 4A and is attached
to a tensioning weight 5. Typically a 20g tensioning weight is used. The other end
of the yarn is attached to a second cord 6 by the metal link 3. Between the metal
links the yarn is twisted about itself in the test region 7 and is weighed down by
passing the yarn around a lower yarn guide pulley 8. The second cord 6 passes over
a second upper yarn guide pulley 9 and is attached to an electrically driven reciprocating
means 10. A beaker 11 is provided for containing water or aqueous media used to test
the yarn in wet conditions.
[0020] The test method consists of attaching the yarn to be tested to one of the metal links,
passing the yarn around the lower yarn guide pulley 9 and then twisting the yarn around
itself a predetermined number of times to form the test region 7, before attaching
it to the other metal link. If required, the beaker is filled with an aqueous test
medium. The reciprocating means is then switched on. A record is kept of the number
of oscillations of the reciprocating means before failure. In each of the following
examples the test was repeated a number of times and very high or low results discarded
before a statistical analysis was made of the remaining data.
Example 1
[0021] 100% extracted Terry Cotton yarns were washed for 15 minutes at 50°C using the recommended
dose of a wasing powder sold under the trade mark "New Persil automatic" and having
the composition:
- 6.0
- Alkyl benzene sulphonate
- 4.5
- Nonionic 7EO
- 3.5
- Nonionic 3EO
- 25.0
- Sodium tripolyphosphate
- 10.0
- perborate tetrahydrate
- 25.0
- sodium sulphate
- 5.0
- sodium carbonate
water and minor ingredients to balance
[0022] The yarns were then rinsed. Some yarns were rinsed in water as a control and others
were rinsed in fabric softening compositionsr. Two fabric softening compositions were
used, one containing the cationic quaternary ammonium Arquad 2HT as the quaternary
ammonium material and the other containing HT TMAPC as the biodegradable cationic
quaternary ammonium material.
[0023] The compositions of the two fabric softening compositions were as follows:
COMPOSITION A
[0024]
- 12.8
- DHTDMAC¹
- 3.2
- HTFA²
- 0.75
- PERFUME
water to balance
1. DHTDMAC is dihardened tallow dimethyl ammonium chloride available as Arquad 2HT
from Akzo Chemie.
2. is hardened tallow fatty acid, Pristerin 4916 ex Unichema.
COMPOSITION B
[0025]
- 11.6
- HT TMAPC³
- 1.9
- HTFA²
- 1.5
- GENAPOL T-150⁴
- 0.75
- PERFUME
water to balance
3. HT TMAPC is 1,2 dihardened tallowoyloxy-3-trimethylammonio propane chloride ex
Hoechst.
4. is tallow alcohol ethoxylated with 15 moles of ethylene oxide.
[0026] The compositions were used at recommended concentrations in cold water. After rinsing,
the yarns were allowed to dry for 24 hours at room temperature. They were then individually
abraided on the yarn on yarn abrasion tester. Abrasion tests were carried out dry
and in washing powder solution. All tests were carried out using tap water at room
temperature.
[0027] Table 1 shows the mean number of cycles before 24 samples of yarn failed in a dry
abrasion test.
TABLE 1
| Treatment |
Number of cycles to failure |
| Water |
964 |
| DHTDMAC |
1503 |
| HT TMAPC |
2407 |
[0028] The difference in the number of cycles to failure between the samples rinsed with
fabric softening composition according to the present invention and the other samples
is very large. In order to check whether the differences were statistically significant
F and T tests were performed on the data. It can be concluded from this analysis that
the use of a fabric conditioner gives reduced fibre damage during the dry abrasion
that would occur when a garment is being worn. Furthermore it can be seen that the
use of a fabric softening composition containing a quaternary ammonium material with
ester linkages according to the present invention provides the best protection. A
photomicrograph of the failed fibre shows that the yarn has not suffered fibrillation
damage.
Example 2
[0029] Example 1 was repeated with the yarn immersed in a solution of "New Persil automatic".
This simulated the effect of a faric softening composition on fibre damage caused
during the next wash. The variation in the number of cycles until breakage in this
example was found to be less than that for example 1. This means that smaller differences
in the mean number of cycles to failure become statistically significant. The results
are given in table 2.
TABLE 2
| Treatment |
Number of cycles to failure |
| Water |
1487 |
| DHTDMAC |
1533 |
| HT TMAC |
1615 |
[0030] Again the use of a fabric softening composition according to the invention is seen
to provide the greatest inhibition of fibre damage. It is important that the fabric
softening composition gives protection in the next wash as well as during wear, because
the garments are particularly prone to damage during the washing process when the
fibres are swollen.
1. Use as fibre damage inhibitor or fibre protector of a fabric softening composition
comprising at least 1% by weight of a quaternary ammonium material having two C₁₂₋₂₈
alkyl or alkenyl groups connected via an ester link to a hydrocarbon chain which is
connected to the quaternary nitrogen atom.
2. Use of a quaternary ammonium material as claimed in claim 1 wherein the fabric softening
composition comprises a nonionic stabilising agent which is
i. a linear C₈ to C₂₂ alcohol alkoxylated with 10 to 20 moles of alkylene oxide or
ii. a C₁₀ to C₂₀ alcohol or mixtures thereof.
3. Use of a quaternary ammonium material as claimed in claim 1 or claim 2 wherein the
fabric softening composition comprises a fatty acid material.
4. Use of a quaternary ammonium material as claimed in claim 2 wherein the composition
comprises from 0.1 to 10% by weight of the nonionic stabilising agent.
5. Use of a quaternary ammonium material as claimed in claim 3 wherein the composition
also comprises more than 0.1% by weight of a fatty acid material.
6. Use of a quaternary ammonium material as claimed in any preceding claim wherein the
composition comprises from 3% to 50% by weight of the quaternary ammonium material,
from 0.5% to 5% by weight of the nonionic stabilising agent and from 0.5 to 20% by
weight of fatty acid material.
7. Use of a quaternary ammonium material as claimed in any one of claims 2 to 6 wherein
the nonionic stabilising agent has an HLB of between 10 and 20.
8. Use of a quaternary ammonium material as claimed in claim 7 wherein the nonionic stabilising
agent has an HLB of between 12 and 20.
9. Use of a quaternary ammonium material as claimed in any preceding claim wherein the
quaternary ammonium material is represented by the formula:

wherein each R₁ group is independently selected from C₁₋₄ alkyl, alkenyl or hydroxyalkyl
groups; and wherein each R₂ group is independently selected from C₈₋₂₈ alkyl or alkenyl
groups; and n is an integer from 0 to 5.