[0001] Current laundry tablets have inferior dispersion/dissolution properties to powders
because of the ability of surfactants to form viscous liquid crystalline phases during
the initial stages of dilution. In a tablet format this leads to pore blockage and
hence inhibition of water ingress which in turn reduces the rate of tablet break-up
and dissolution.
[0002] Typically current laundry tablets contain mainly soluble surfactants such as linear
alkylbenzene sulphonates (=LAS), primary alkyl sulphates (=PAS) and nonionics. It
is known that the use of low levels of non-ionics prevents bleeding, whereas bleeding
during storage is further prevented by the addition of a small amount of insoluble
soap to the non-ionic(s). The maximum ratio of soap/non-ionic is said to be ca 0.2,
preferably about 0.1 and even more preferred about 0.033 (ref WO 9842817). The soap
that is present is said to aid tabletting, (ref WO9842817) but higher ratios of soap/non-ionic
are said to lead to unsatisfactory results.
[0003] Surprisingly we have found that incorporation of insoluble soaps into the anionic
surfactant alone or in both the anionic and non-ionic surfactants in a specific form
leads to superior tablet dispersion/dissolution properties.
[0004] The mechanism of this action is not clear but some scientists believe that the structuring
effects of the soap on the soluble surfactants plays a role and therewith the rate
of water uptake. We now found that the physical form wherein the soap and surfactants
are added plays a role as well and that by careful balancing of the ratio of the low
solubility soap(s) to in particular the anionic surfactant(s) and by applying a special
preparation method for these blends the solubility of the blend can be designed so
that negligible dissolution occurs during the initial critical stage of tablet wetting
out.
Another parameter that plays a role seems the ratio of soap to total of anionic and
non-ionic surfactants, while also the Tk of the soap is important. The Tk of the soap
is defined as below.
The soluble-surfactant/low solubility soap particles subsequently disperse into the
bulk wash solution and then dissolve.
[0005] This invention not only enhances the rate of tablet dispersion/dissolution, expressed
as T90 and measured by the method disclosed e.g. in the examples of WO 00/22089 ,
but as a result of this improvement, also reduces the risk of residues and patch damage.
[0006] Tablets that comprise low solubility soap and anionics in ratios of about 0.1 are
disclosed in e.g. US 5 900 399 (examples 1 and 2); in EP 716 144 (examples) tablets
are disclosed wherein the ratio between a non specified soap and anionics ranges from
about 2.3 to about 0.4, while the ratio between the soap and the total of anionics
and non-ionics herein is about 0.1 to 0.2. Still these tablets do not display satisfying
dissolution properties. This is due, as we found, to the fact that the soap and anionics
are not added in the correct physical form. We found that if first a coagel is made
from at least the anionics (but the non-ionics can be present as well) and the low
solubilty soap and this coagel is added to the tablets the dissolution properties
improved considerably.
[0007] A coagel is defined here as a thermoreversible gel, which is formed by spontaneous
separation of an anisotropic interconnected solid network from an isotropic continuum.
These structures provide high gel-strengths with relatively low solids content, due
to their high degree of interconnectivity (cf Cahn c.s in J Chem Phys 31, 1959 p.
688 and 42, 1965, p 93)
[0008] One way to make a coagel of these ingredients is to contact a mix of solid carrier
material, in particular a mix of zeolite and soda ash with at least part of the free
fatty acid constituents of the low solubility soap and the acidic form of anionic
surfactants (optionally in the presence of non-ionic surfactants) and then neutralise
the acids by an in-situ neutralisation reacting the soda ash which is part of the
carrier material with the acids. In fact we prefer to make the coagel by an in-situ
neutralisation of a mix of at least the anionics and the free fatty acid constituents
of the soap using an alkali reagent.
Therefore our invention concerns in the first instance novel laundry tablets comprising
granules wherein soap and surfactants are present and wherein the surfactants comprise
either one or more anionic surfactants or a mix of one or more anionic and one or
more non-ionic surfactants and wherein the soap has a Tk of at least 35°C while the
weight ratio of soap to anionic surfactants is at least 0.1, preferably 0.1 to 0.5
and the weight ratio of soap to total surfactants is less than 0.5.
The soap can be present as a coagel with the anionics only but also coagels of soap
and all surfactants present lead to good results. The laundry tablet so-formed has
enhanced dispersion/dissolution properties while maintaining tablet integrity. This
integrity can be expressed as Fmax, which is measured by the method disclosed in the
examples of WO 00/22089
[0009] Very convenient soaps are soap derived from one or more fatty acids selected from
the group consisting of straight chain fatty acids with 12 to 24 carbon atoms.
The "low solubility soap" is defined by its solubility in water expressed as a Kraft
temperature, (Tk value, i.e. the minimum solubility temperature for the soap corresponding
to the crystal solubility boundary). The target minimum value for this Tk is 35°C.
Examples of suitable soaps include those selected from one or more of saturated and
unsaturated alkyl carboxylates where the counterion is one of sodium, potassium, calcium
or magnesium. The soap or blend must have a Tk value in excess of 35 Celsius. Examples
of single soaps include sodium laurate, sodium myristate, sodium palmitate, sodium
stearate, sodium behenate, potassium palmitate, potassium stearate and calcium laurate.
Examples of blends include blends from 99/1 to 1/99 of sodium soaps of palmitate and
myristate, palmitate and stearate, and myristate and stearate. Examples of blends
containing unsaturated alkyl soaps include less than 1:1 blends of sodium oleate and
sodium stearate and sodium oleate and sodium palmitate.
[0010] Other components can also be post dosed to the compositions. Preferred additional
components are urea and sodium carbonate. Other components include one or more detergency
builders, bleaches, bleach precursors and optionally other detergent ingredients.
[0011] The soluble surfactants are usually comprised of one or more anionic and nonionic
surfactants but can also include amphoteric and cationic surfactants. Typically the
anionic surfactant is selected from LAS and PAS. Typically the nonionic surfactants
are selected from alcohol ethoxylates. The amphoteric surfactants are typically betaine-type
derivatives.
[0012] Synthetic (i.e. non-soap) anionic surfactants are well known to those skilled in
the art. Examples include alkyl benzene sulphonates (= LAS), particularly sodium linear
alkyl benzene sulphonates having an alkyl chain length of C
8-C
15; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid
ester sulphonates.
[0013] Primary alkyl sulphate (= PAS) having the formula:
ROSO
3- M
+
in which R is an alkyl or alkenyl chain of 8 to 18 carbon atoms especially 10 to 14
carbon atoms and M
+ is a solubilising cation, is commercially significant as an anionic surfactant.
[0014] Linear alkyl benzene sulphonate of the formula;

where R is linear alkyl of 8 to 15 carbon atoms and M
+ is a solubilising cation, especially sodium, is also a commercially significant anionic
surfactant.
[0015] Suitable nonionic surfactant compounds which may be used include in particular the
reaction products of compounds having a hydrophobic group and a reactive hydrogen
atom, for example, aliphatic alcohols, acids, amides or alkyl phenols with alkylene
oxides, especially ethylene oxide.
[0016] Specific nonionic surfactant compounds are alkyl (C
8-22) phenolethylene oxide condensates, the condensation products of linear or branched
aliphatic C
8-20 primary or secondary alcohols with ethylene oxide, and products made by condensation
of ethylene oxide with the reaction products of propylene oxide and ethylene-diamine.
[0017] Especially preferred are the primary and secondary alcohol ethoxylates, especially
the C
9-11 and C
12-15 primary and secondary alcohols ethoxylated with an average of from 5 to 20 moles
of ethylene oxide per mole of alcohol.
[0018] The coagel of soluble and insoluble surfactants necessary for the invention can also
be made by a process wherein the in-situ neutralisation of the acids is performed
by using an alkali reagent of a co-injected mix of anionic surfactants and the free
fatty acid constituent of the soap during an NTR processing.
[0019] The granules that can be applied can be the result of a spray drying process.
[0020] The preferred process for the preparation of our novel laundry tablets involves the
following steps:
- first granules are made by a process wherein solid carrier material, in particular
a mix of zeolite and soda ash is contacted with at least part of the free fatty acid
consistuents of a low solubility soap and the acidic form of anionic surfactants,
optionally in the presence of non-ionic surfactants
- whereupon the acids are neutralised in -situ by reacting with the soda ash which is
part of the carrier material
- the coagel so obtained is mixed with the other components of the tablet
- and the tablet is formed by compressing a premoulded amount of granules
[0021] According to a preferred embodiment the neutralisation reaction between acids and
soda ash is performed in a high shear solid mixer.
[0022] Other tablet components typically include builders, bleaches, bleach precursors,
optical brighteners, polymers, electrolytes, fillers, organic disintegrants and clays
The following examples illustrate the Invention:
Example 1: Control product
[0023] In this example of a control product, the insoluble sodium soap, (1:1 blend of C16
and C18 fatty acids which are subsequently neutralised during processing) is mixed
with the nonionic surfactant to prevent bleeding on storage. No soaps are blended
with the anionic surfactant. The ratio of insoluble soap/ nonionic surfactants is
ca 1.6/10, and the ratio of insoluble soap/total soluble surfactants is 0.7/10.
Process details; All powders (except Zeolite A24 layer) added to FS100 batch high
shear granulator. Powders premixed. The LAS acid is heated to approx 70°c and added
to the powder.
The nonionic (7EO plus 3EO) / fatty acid mixture, (ratio nonionic/soap = 1.6/10) is
heated to approx. 70°c and is poured into the mixer. Following granulation the mixer
is stopped and the layer is then added onto the top of the granules. The mixer is
started and the product is discharged. Base powder was sieved and the cut used was
850-1400µm. This base powder was then mixed with post-dosed ingredients to give the
full formulation of Table 2.
Table 1:
Control product - (wgt%) |
Formulation |
Control |
LAS Acid |
18.67 |
NI 7eo |
5.93 |
NI 3eo |
3.11 |
Pristerine 4916 (A fully hardened tallow fatty acid soap) |
1.46 |
Na Acetate |
5.93 |
Light Soda Ash (LSA) |
12.64 |
Sodium carboxymethyl Cellulose (SCMC) |
0.88 |
Zeolite A24 |
48.76 |
Zeolite Layer |
2.63 |
Table 2:
Full formulation details (wgt %) |
Formulation |
Control |
Base Powder |
46.40 |
Anti foam granule |
1.80 |
NaPercarbonate |
15.00 |
Tetraacetyl ethylene diamine (TAED) |
5.10 |
Anti redeposition polymer |
5.50 |
NaCarbonate dense |
1.40 |
NaAcetate |
24.90 |
[0024] The gross tablet properties of hardness, (expressed as Fmax) and solubility, (expressed
as T90) are shown in Table 3.
Table 3:
Target Fmax for tablets 35N (i.e. Day 0 value) |
Control |
|
|
Time (week) |
Fmax |
T90 |
0 |
36.1 |
248.2 |
1 |
35.38 |
271.52 |
4 |
34.29 |
250.2 |
[0025] Example 2: This product contains a blend of insoluble sodium soap, (derived from C14 fatty acid)
blended with the anionic surfactant, (LAS) with a soap/LAS ratio = ca 1.6/10 and a
soap/total soluble surfactant, (LAS + Nonionic) ratio = 1/10. In this product, no
soap is present in the nonionic surfactants.
The base detergent formulation is given in Table 4.
Table 4 -
(wgt %) |
Formulation |
LAS Acid |
18.4 |
NI 7eo |
5.8 |
NI 3eo |
3.0 |
Na Acetate |
5.8 |
LSA |
12.4 |
SCMC |
0.9 |
Myristic acid 2914 |
2.8 |
Zeolite A24 |
48.2 |
Zeolite A24 layer |
2.6 |
[0026] Process details; All powders (except Zeolite A24 layers) added to FS100 batch high
shear granulator. Powders premixed. The LAS acid and merits acid mixture is heated
to approx. 70°c and added to the powder.
The nonionic (7EO plus 3EO) mixture is heated to approx. 70°c and is poured into the
mixer. Following granulation the mixer is stopped and the layer is then added onto
the top of the granules. The mixer is started and the product is discharged. Base
powder was sieved and the cut used was 850-1400µm.
[0027] Full formulation details (wet %) after addition of post-dosed ingredients are given
in Table 5.
Table 5:
Formulation |
Control |
Base Powder |
46.40 |
Anti foam granule |
1.80 |
NaPercarbonate |
15.00 |
TAED |
5.10 |
Anti redeposition polymer |
5.50 |
NaCarbonate dense |
1.40 |
NaAcetate |
24.90 |
[0028] This powder was subsequently tabletted to a target hardness of 35 Newton's. The gross
tablet properties are given in Table 6.
Table 6:
2.5% Myristate in LAS I |
Time (week) |
Fmax |
T90 |
0 |
30.0 |
213.9 |
1 |
33.05 |
237.62 |
4 |
33.20 |
208.5 |
[0029] Comparison of the gross tablet properties of this product and the control product
of Example 1 shows that this product has similar hardness but faster dissolution time.
[0030] Example 3 - this product contains C14 soap, (myristate) blended in with both LAS and nonionics.
The ratio of soap/LAS= 0.8/10 and the soap/nonionics = 2/10. The ratio of soap/total
soluble surfactants = 1/10. The base detergent formulation is given in
Table 7:
(wgt %) |
Formulation |
LAS Acid |
16.64 |
NI 7eo |
5.27 |
NI 3eo |
2.73 |
Myristate 2914 |
2.55 |
Na Acetate |
5.27 |
LSA |
11.27 |
SCMC |
0.73 |
Zeolite A24 |
53.18 |
Zeolite Layer |
2.36 |
[0031] Process details; All powders (except Zeolite A24 layer) added to FS100 batch high
shear granulator. Powders premixed. The LAS acid and half of the myristic acid mixture
is heated to approx 70°c and added to the powder.
The nonionic (7EO plus 3EO) containing the remaining half of the myristic acid is
heated to approx. 70°c and is poured into the mixer. Following granulation the mixer
is stopped and the layer is then added onto the top of the granules. The mixer is
started and the product is discharged. Base powder was sieved and the cut used was
850-1400µm.
Full formulation details (wgt %) |
Formulation |
Control |
Base Powder |
46.40 |
Anti foam granule |
1.80 |
NaPercarbonate |
15.00 |
TAED |
5.10 |
Anti redeposition polymer |
5.50 |
NaCarbonate dense |
1.40 |
NaAcetate |
24.90 |
|
|
Target Fmax for tablets 35N (i.e. Day 0 value) |
2.5% Myristate in LAS and NI |
Time
(week) |
Fmax |
T90 |
0 |
33.80 |
220.70 |
1 |
36.20 |
227.10 |
4 |
35.44 |
236.0 |
[0032] Comparison of the gross tablet properties of this product and the control product
of Example 1 show this product to have similar hardness but faster dissolution time.
[0033] Example 4 - this product contains C14 soap, (myristate) blended in with both LAS and nonionics.
The ratio of soap/LAS= 2/10 and the soap/nonionics = 4/10. The soap/total soluble
surfactant ratio = 2.7/10. The base detergent formulation is given in Table 8.
Table 8:
(wgt %) |
Formulation |
LAS Acid |
14.56 |
NI 7eo |
4.63 |
NI 3eo |
2.37 |
Myristate 2914 |
5.60 |
Na Acetate |
4.20 |
LSA |
8.87 |
SCMC |
0.57 |
Zeolite A24 |
55.21 |
Zeolite Layer |
3.99 |
[0034] Process details; All powders (except Zeolite A24 layer) added to FS100 batch high
shear granulator. Powders premixed. The LAS acid and half of the myristic acid mixture
is heated to approx 70°c and added to the powder.
The nonionic (7EO plus 3EO) containing the remaining half of the myristic acid is
heated to approx. 70°c and is poured into the mixer. Following granulation the mixer
is stopped and the layer is then added onto the top of the granules. The mixer is
started and the product is discharged. Base powder was sieved and the cut used was
850-1400µm.
Table 9
Full formulation details (wgt %) |
Formulation |
Control |
Base Powder |
46.40 |
Anti foam granule |
1.80 |
NaPercarbonate |
15.00 |
TAED |
5.10 |
Anti redeposition polymer |
5.50 |
NaCarbonate dense |
1.40 |
NaAcetate |
24.90 |
Table 10
Target Fmax for tablets 35N (i.e. Day 0 value) |
5% Myristate in LAS and NI |
Time
(week) |
Fmax |
T90 |
0 |
25.20 |
132.20 |
1 |
28.94 |
146.44 |
4 |
27.20 |
139.40 |
[0035] Comparison of the gross tablet properties of this product and the control product
of Example 1 show this product to have similar hardness but faster dissolution time.
[0036] Example 5: In this product we have used C14 soap to structure the LAS and nonionics with soap/LAS
ratio = 3.8/10 and soap/nonionic ratio = 8/10. The ratio of soap/total soluble surfactants
= 5.1/10.
The base detergent formulation is given in Table 11.
Table 11:
Formulation |
LAS Acid |
12.93 |
NI 7eo |
4.12 |
NI 3eo |
2.15 |
Na Acetate |
4.12 |
LSA |
8.71 |
SCMC |
0.56 |
Myristate 2914 |
9.37 |
Zeolite A24 |
54.11 |
Zeolite Layer |
3.93 |
[0037] Process details; All powders (except Zeolite A24 layer) added to FS100 batch high
shear granulator. Powders premixed. The LAS acid and half of the myristic acid mixture
is heated to approx 70°C and added to the powder.
The nonionic (7EO plus 3EO) containing the remaining half of the myristic acid is
heated to approx 70°C and is poured into the mixer. Unfortunately at this high level
of incorporation of myristic acid it was not possible to produce an acceptable base
powder due to the high liquids content prior to neutralisation. This example thus
illustrates that there is maximum level of soap that can be incorporated in the tablets.
Examples 6A and 6B
[0038] In these products we have made the control formulation of Example 1 to a different
tablet hardness and coded this product 'Example 6A'. In addition we have made a further
product, 'Example 6B' by using a soluble soap blend, (sodium oleate/sodium linoleate)
to structure the LAS and nonionics with soap/LAS ratio = 1.9/10 and soap/nonionic
ratio = 4.1/10 in Example 6B. This soap blend falls outside the scope of the requirement
that the Tk of the soap being >35°C. The actual Tk of the sodium soap of Priolene
6930 will be ca 15°C.
The base detergent formulation for Example 6B is given
Table 12
Formulation |
LAS Acid |
14.56 |
NI 7eo |
4.63 |
NI 3eo |
2.37 |
Priolene 6930 |
5.60 |
Na Acetate |
4.20 |
LSA |
8.87 |
SCMC |
0.57 |
Zeolite A24 |
55.21 |
Zeolite Layer |
3.99 |
[0039] Process details; All powders (except Zeolite A24 layer) added to FS100 batch high
shear granulator. Powders premixed. The LAS acid and half of the priolene fatty acid
mixture is heated to approx. 70°C and added to the powder.
The nonionic (7EO plus 3EO) containing the remaining half of the priolene acid is
heated to approx. 70°C and is poured into the mixer. Following granulation the mixer
is stopped and the layer is then added onto the top of the granules. The mixer is
started and the product is discharged. Base powder was sieved and the cut used was
850-1400µm.
Full formulation details (wgt %) |
Formulation |
Control |
Base Powder |
46.40 |
Anti foam granules |
1.80 |
NaPercarbonate |
15.00 |
TAED |
5.10 |
Anti redeposition polymer |
5.50 |
NaCarbonate dense |
1.40 |
NaAcetate |
24.90 |
|
Fmax and T90 data: |
|
Control (6A) |
Product 6B |
Fmax (N) |
22 |
18 |
T90 (s) |
120 |
120 |
[0040] Comparison of the gross tablet properties of these products show that the product
6B made at similar hardness to the control product has an identical dissolution time.
Hence use of the soluble soap has not delivered any improvement in dissolution properties
[0041] Examples 7 and 8: In these examples the control base powder of example 1 is made and the postdose
ingredients, are as shown in Table 13 with the Fmax values as given.

[0042] The T90 values are clearly superior when the sodium acetate is replaced by urea,
even though the tablet hardness is greater in the urea containing tablet.
[0043] Example 8: In this example the base powder of Example 2 has been used with the post dose ingredients
as shown in Table 14.

[0044] The T90 values are substantially shorter than those of Example 7 where an identical
post-dose was used. This confirms that the combination of modified base and urea.soda
ash post dose work together to deliver a further improvement in dissolution.
[0045] Example 9: In this example the base powder of Example 3 has been used with the postdose ingredients
as shown in Table 15.

[0046] As in the previous example the combination of modified base and selected post dose
ingredients provides a combined decrease in T90, i.e. improved dissolution relative
to the conventional base of Example 7.
[0047] Example 10: In this example the base powder of Example 4 has been used with the postdose ingredients
as shown in Table 16. The T90 value is less than that of Example 7 where the conventional
base is used.

1. Laundry tablet comprising granules wherein soap and surfactants are present and wherein
the surfactants comprise either one or more anionic surfactants or a mix of one or
more anionic and one or more non-ionic surfactants, the soap being a low water-soluble
soap which is present as a coagel with at least the anionic surfactants and wherein
the soap has a Tk of at least 35°C while the weight ratio of soap to anionic surfactants
is at least 0.1, preferably 0.1 to 0.5 and the weight ratio of soap to total surfactants
is less than 0.5.
2. Laundry tablet according to claim 1 wherein the soap is present as a coagel with all
surfactants.
3. Laundry tablet according to claims 1 and 2 wherein the coagel of soap and surfactants
is the result of an in-situ neutralisation of a mix of at least the anionic surfactants
and the free fatty acid constituents of the soap using an alkali reagent.
4. Laundry tablet according to claims 1 to 3 wherein the soap is derived from one or
more fatty acids selected from the group consisting of straight chain fatty acids
with 12 to 24 C-atoms.
5. Laundry tablet according to claims 1 to 4 wherein the coagel of soap and surfactants
is present in the form of granules which have a soap content of maximum 10 wt % .
6. Laundry tablet according to claims 1 to 5 wherein the granules are the result of a
spray drying process.
7. Laundry tablet according to claims 1 to 6 wherein the tablets contain post dosed ingredients
in particular urea and soda ash.
8. Process for the preparation of laundry tablets with the composition according to claims
1 to 7 wherein tablets are made by a process wherein first granules are made by a
process wherein solid carrier material, in particular a mix of zeolite and soda ash
is contacted with at least part of the free fatty acid constituents of a low solubilty
soap and the acidic form of anionic surfactants, optionally in the presence of non-ionic
surfactants whereupon the acids are neutralised in-situ by reacting with the soda
ash which is part of the carrier material to form a coagel whereupon the other components
of the tablet are added and the tablets are formed by compressing a premoulded amount
of granules
9. Process according to claim 8 wherein the neutralisation reaction between acids and
soda ash is performed in a high shear solid mixer.