[0001] This invention relates to detergent compositions, and in particular those containing
lipolytic enzyme.
[0002] Detergent compositions comprising lipase are known. For example GB 1 372 034 (Unilever)
discloses lipase from Pseudomonas in specific nonionic-containing [detergent] compositions
for soaking fabrics.
[0003] USP 3 950 277 (Procter & Gamble) also describes fabric-soaking compositions: the
described compositions comprise lipase and lipase activators and a number of lipases
from microorganism and other sources are mentioned: those particularly mentioned as
preferred are Amano CE, Amano M-AP, Takeda 1969-4-9, and Meito MY-30 lipases, but
no indications are given of the form in which the lipase is to be prepared or used.
[0004] USP 4 011 169/NL 74 08763 (Procter & Gamble) describes the use of a similar range
of enzymes in the preparation of additives for washing agents (detergent compositions).
EP 0 214 761 (Novo) and EP 0 258 068 (Novo), each give detailed description of lipases
from certain microorganisms, and also give certain uses in detergent additives and
detergent compositions for the enzymes described. EP 0 214 761 gives detailed description
of lipases derived from organisms of the species Pseudomonas cepacia, and certain
uses therefor. EP 0 258 068 gives detailed description of lipases derived from organisms
of the genus Thermomyces/Humicola, and certain uses therefor.
[0005] Also believed to be in use in certain areas is a lipase-containing granular detergent
composition containing about 37% detergent actives including 5% nonionic detergent
and the remainder substantially anionic detergent, about 16% zeolite, about 70-90
LU/g lipase, plus protease and other normal detergent additives.
[0006] An aim of this invention is the provision of a lipase-containing granular detergent
composition with a particularly effective formulation for supporting the action of
lipase enzyme.
[0007] According to the present invention, there is provided a granular detergent composition
or component therefor, which comprises:
(a) from 6% to 35%, often over 17%, by weight of non-soap detergent-active material
consisting at least partially of anionic and/or nonionic detergent-active material;
(b) at least 45% by weight of builder,
(b1) the builder including at least 28%, e.g. up to 45%, by weight (anhydrous basis)
of crystalline or amorphous sodium aluminosilicate and/or citrate, carbonate, or layered
silicate builder,
(c) a lipolytic enzyme,
the weight ratio of (b1) to (a) being from 0.9:1 to 2.6:1, preferably from 1.2:1
to 1.8:1; and other detergent ingredients to 100% by weight.
[0008] According to the invention, certain of the compositions and components (adjuncts)
therefor, including preferred compositions, can be prepared by treating a particulate
starting material comprising:
(a) from 5 to 35% by weight of non-soap detergent-active material consisting at least
partially of anionic detergent-active material, and
(b) from 28 to 45% by weight (anhydrous basis) of crystalline or amorphous sodium
aluminosilicate, the weight ratio of (b) to (a) being at least 0.9:1, and other detergent
components to 100% by weight,
in a high-speed mixer in the presence of a liquid binder but in the absence of a
finely divided particulate agent for improving surface properties, whereby granulation
and densification to a bulk density of at least 650 g/litre are effected, and adding
a lipolytic enzyme preparation after the granulation stage which has been carried
out in the high-speed mixer.
[0009] Certain embodiments of the invention have a high bulk density, e.g. a bulk density
of at least 650 g/litre.
[0010] It is useful and surprising that lipase activity is particularly well supported in
the presence of the quantities of builder set out herein.
[0011] The lipolytic enzyme can usefully be added in the form of a granular composition
of lipolytic enzyme with carrier material.
[0012] The added amount of lipolytic enzyme can be chosen within wide limits, for example
30 to 30,000 LU/g of granular detergent composition, e.g. at least 300 LU/g, often
usefully at least 500 LU/g, sometimes preferably above 1000 LU/g or above 3000 LU/g
or more.
[0013] Ihe lipolytic enzyme can be chosen from among a wide range of lipases: in particular
the lipases described in for example the following patent specifications, EP 0214761
(Novo), EP 0258068 (Novo) and especially lipases showing immunological cross-reactivity
with antisera raised against lipase from Thermomyces lanuginosus ATCC 22070, EP 0205208
(Unilever) and EP 0206390 (Unilever), and especially lipases showing immunological
cross-reactivity with antisera raised against lipase with Chromobacter viscosum var
lipolyticum NRRL B-3673, or against lipase from Alcaligenes PL-679, ATCC 31371 and
FERM-P 3783, also the lipases described in specifications WO 87/00859 (Gist-Brocades)
and EP 0204284 (Sapporo Breweries). Suitable in particular are for example the following
commercially available lipase preparations: Novo Lipolase, Amano lipases CE, P, B,
AP, M-AP, AML, and CES, and Meito lipases MY-30, OF, and PL, also esterase MM, Lipozym,
SP225, SP285, Saiken lipase, Enzeco lipase, Toyo Jozo lipase and Diosynth lipase (Trade
Marks).
[0014] It has now been surprisingly found that lipolytic enzyme exerts a comparatively greater
effect when used in compositions of the type described above, than when used in comparative
compositions as illustrated in the lipolytic example below.
[0015] According to preferred embodiments, the invention provides detergent powders combining
high bulk density, good powder properties and excellent washing and cleaning performance,
that can be prepared easily and conveniently.
[0016] These detergent compositions owe their combination of excellent properties and ready
processability to a moderate content of surfactant, at least part of which is anionic,
and a relatively high level of sodium aluminosilicate builder. It has been found that
when the absolute amounts of aluminosilicate builder and surfactant, and the ratio
of one to the other, are suitably chosen, the spray-dried base powder may be pulverised
and granulated in a high-speed mixer without the need for the use of an "agent for
improving surface properties" during the granulation step as prescribed by JP 61 069897A
(Kao). The resulting dense granulate has good flow properties and is at least equal
in washing and cleaning performance and cold water dispersability to the compositions
described in the Kao specification which contain substantially higher levels of surfactant.
[0017] The aluminosilicate builder present in the compositions may be crystalline or amorphous
or a mixture thereof, and can have the general formula
0.8-1.5 Na2O . A12O3 . 0.8-6 SiO2.
[0018] These materials contain some bound water and should in most cases have a calcium
ion exchange capacity of at least about 50 mg CaO/g. The preferred aluminosilicates
contain 1.5-3.5 SiO2 units (in the formula above) and have a particle size of not
more than about 100 microns, preferably not more than about 20 microns. Both amorphous
and crystalline aluminosilicates can be made readily by reaction between sodium silicate
and sodium aluminate, as amply described in the literature.
[0019] Crystalline aluminosilicates (zeolites) are preferred for use in the present invention.
Suitable materials are described, for example, in GB 1 473 201 (Henkel) and GB 1 429
143 (Procter & Gamble). The preferred sodium aluminosilicates of this type are the
well-known commercially available zeolites A and X, and mixtures thereof. Especially
preferred for use in the present invention is Type 4A zeolite.
[0020] The ratio of aluminosilicate builder (anhydrous basis) to total non-soap surfactant
in the compositions is preferably within the range of from 1.2:1 to 1.8:1.
[0021] The non-soap surfactant present consists at least partially of anionic surfactant.
Suitable anionic surfactants are well known to those skilled in the art, and include
linear alkylbenzene sulphonates, primary alcohol sulphates, alkyl ether sulphates,
alpha-olefin sulphonates, internal olefin sulphonates, fatty acid ester sulphonates
and combinations thereof.
[0022] If desired, nonionic surfactant may also be present, preferably in a minor amount.
Suitably the surfactant component of the compositions of the invention may be constituted
by 10 to 35% by weight of anionic surfactant and 0 to 10% by weight of nonionic surfactant.
[0023] If desired, soap may also be present, to provide foam control and additional detergency
and builder power; soap is not included in the 17 to 35% figure given above for the
total surfactant content of the compositions.
[0024] The compositions preferably do not contain more than 5% by weight of phosphate builders,
and are more preferably substantially free of phosphate builders.
[0025] The particulate starting composition may be prepared by any suitable tower or non-tower
method, for example, spray-drying or dry-mixing; spray-drying is preferred.
[0026] The final granulate may be used as a complete detergent composition in its own right.
Alternatively, additional ingredients such as enzymes, bleach and perfume that are
not suitable for undergoing the granulation process and the steps that precede it
may be admixed to the granulate to make a final product.
[0027] In preferred cases the final granulate has a bulk density of at least 650 g/litre
and more preferably at least 700 g/litre. It is preferably also characterised by an
especially low particle porosity, not exceeding 25% and preferably not exceeding 20%,
which distinguishes it from even the densest powders prepared by spray-drying alone.
[0028] In suitable examples of processes for making the preferred high-bulk-density compositions,
a particulate starting material (detergent base powder) prepared by any suitable method
is treated in a high-speed mixer to increase its bulk density and simultaneously to
improve its powder properties. The process is especially useful for the densification
of a spray-dried powder, and provides a route for the production of very dense granular
detergent compositions, having excellent cleaning performance, containing low to moderate
levels of anionic surfactant and high levels of aluminosilicate builder.
[0029] A preferred starting powder comprises:
(a) from 17 to 35% by weight of non-soap detergent-active material consisting at least
partially of anionic detergent-active material, and
(b) from 28 to 45% by weight of crystalline or amorphous sodium aluminosilicate,
the weight ratio of (b) to (a) being from 0.9:1 to 2.6:1, and other detergent components
to 100% by weight.
[0030] On treatment in a high-speed mixer by an example of the process set out above, this
can gives a granular detergent composition or component of the preferred high bulk
density: it will be noted, however, that the process also gives good results with
compositions containing lower levels of detergent-active material.
[0031] For carrying out the process, a mixer is apparently required that combines a high
energy stirring input with a cutting action. The Fukae (Trade Mark) FS-G mixer manufactured
by Fukae Powtech Kogyo Co., Japan, has been found to give excellent results in batchwise
operation. This apparatus is essentially in the form of a vessel accessible via a
top port, provided near its base with a stirrer having a substantially vertical axis,
and a cutter positioned on a side wall. The stirrer and cutter may be operated independently
of one another, and at separately variable speeds.
[0032] Other mixers suitable for use in the process include the Diosna (Trade Mark) V series
ex Dierks & Söhne, Germany; the Lödige (Trade Mark) FM series ex Morton Machine Co.
Ltd., Scotland; and the Pharma Matrix (Trade Mark) ex T K Fielder Ltd., England. Other
mixers believed to be suitable for use in the process are the Fuji (Trade Mark) VG-C
series ex Fuji Sangyo Co., Japan; the Lödige MTG ex Morton Machine Co. Ltd., Scotland;
and the Roto (Trade Mark) ex Zanchetta & Co srl, Italy. The Lödige FM mixer differs
from the Fukae mixer mentioned above in that its stirrer has a horizontal axis; this
configuration is suitable for continuous operation.
[0033] As indicated above, the use of a high speed mixer is essential in the process set
out above to effect granulation and densification. Some starting powders require pulverisation
before granulation can take place; whether or not this is necessary depends, among
other things, on the method of preparation of the starting powder and its free moisture
content. Powders prepared by spray-drying, for example, are more likely to require
pulverisation than powders prepared by dry-mixing. Pulverisation may, if desired,
be carried out as a separate process step, in any suitable separate apparatus, before
granulation in the high speed mixer is carried out. It is convenient, however, to
use the same high-speed mixer for the pulverisation step as for the granulation step.
The high speed mixer may be used for the pulverisation step by running the mixer at
high speed, using both stirrer and cutter. A relatively short residence time (for
example, 2-4 minutes for a 35 kg batch) is generally sufficient. A mass of finely
divided powder is obtained.
[0034] The granulation step follows, and it is during that stage that densification to very
high values of at least 650 g/litre, preferably at least 700 g/litre can be achieved,
giving a dense, granular product of very uniform particle size and generally spherical
particle shape. The final bulk density can be controlled by choice of residence time,
and it has been found that the powder properties of the resulting granulate are best
if the bulk density has been allowed to rise to at least 650 g/litre.
[0035] The presence of a liquid binder is necessary for successful granulation. The amount
of binder added preferably does not exceed that needed to bring the free moisture
content of the composition above about 6% by weight, since higher levels lead to a
deterioration in the flow properties of the final granulate. If necessary, binder,
preferably water, may be added before or during granulation, but some starting powders
will inherently contain sufficient moisture. In the Fukae mixer, granulation is effected
by running the mixer at a relatively high speed using both stirrer and cutter; a relatively
short residence time (for example, 5-8 minutes for a 35 kg batch) is generally sufficient.
If a liquid binder is to be added, it may be sprayed in while the mixer is running.
In one preferred mode of operation, the mixer is first operated at a relatively slow
speed while binder is added, before increasing the speed of the mixer to effect granulation.
[0036] If the starting powder has a sufficient free moisture content to render the addition
of a binder unnecessary, pulverisation (if required) and granulation need not be regarded
as separate process steps but as one single operation. Indeed, it is not, in that
case, necessary to decide in advance whether or not pulverisation is required: the
mixer may simply be allowed to do what is necessary, since the mixer conditions required
are substantially the same for pulverisation and for granulation.
[0037] In general, it is highly preferred that during granulation no "agent for improving
surface properties" as defined in the above-mentioned JP 61 069897A (Kao) be present.
When processing a formulation having a relatively high ratio of aluminosilicate builder
to surfactant, in accordance with examples of the present invention, the use of a
finely divided particulate material such as fine sodium aluminosilicate during the
granulation step is not only unnecessary but can with some formulations make granulation
more difficult, or even impossible.
[0038] In accordance with a preferred embodiment of the invention, a finely divided particulate
flow aid may be admixed with the granular material after granulation is complete.
Advantageously, flow aid is added while the granulate is still in the high-speed mixer,
and the mixer is operated at a slow speed for a further short period. No further granulation
occurs at this stage. It is also within the scope of the invention to add the flow
aid to the granulate after removing the latter to different apparatus.
[0039] This embodiment of the invention should be distinguished from the prior art process
of JP 61 069897A (Kao), mentioned above, in which an "agent for improving surface
properties", which can be fine sodium aluminosilicate, is present during the granulation
stage itself. It is within the scope of the present invention to add a particulate
flow aid after granulation is complete, but, as explained above, it is essential to
the invention that no finely divided particulate "agent for improving surface properties"
be present during granulation. The addition of a flow aid after granulation is complete
can have an additional beneficial effect on the properties of the granulate, regardless
of the formulation, whereas the presence of this type of material during the granulation
step in the present process makes processing more difficult.
[0040] According to a preferred embodiment of the process, granulation is carried out at
a controlled temperature somewhat above ambient, preferably above 30 deg C. The optimum
temperature is apparently formulation-dependent, but appears generally to lie within
the range of from 30 to 45 deg C, preferably about 35 deg C. This temperature may
also be maintained during the subsequent admixture of a flow aid.
[0041] The flow aid is a finely divided particulate material. The preferred average particle
size is 0.1 to 20 microns, more preferably 1 to 10 microns. Substantially amorphous
materials are preferred.
[0042] According to a highly preferred embodiment, the flow aid is finely divided amorphous
sodium aluminosilicate. This material is effective in improving flow properties even
at very low levels, and also has the effect of increasing bulk density. It is therefore
possible to adjust bulk density by appropriate choice of the level of amorphous sodium
aluminosilicate added after granulation.
[0043] A suitable material is available commercially from Crosfield Chemicals Ltd, Warrington,
Cheshire, under the trade mark Alusil. Other flow aids manufactured by this company
include Neosyl (Trade Mark) precipitated silica and Microcal (Trade Mark) precipitated
calcium silicate.
[0044] The flow aid is advantageously used in an amount of from 0.2 to 5.0% by weight, based
on the starting powder, more preferably from 0.5 to 3.0% by weight.
[0045] Zeolite (hydrated crystalline sodium aluminosilicate) is substantially less effective
as a flow aid in the context of the present invention. Substantially higher levels
than those quoted above are needed before any flow or bulk density benefit is observed.
[0046] The invention is illustrated by the following non-limiting Examples, in which parts
and percentages are by weight unless otherwise stated.
Example 1
[0047] A detergent composition is prepared to the following composition by spray-drying
an aqueous slurry to a free moisture content of substantially zero:
|
parts |
Linear alkylbenzene sulphonate |
24.0 |
Nonionic surfactant |
2.0 |
Soap |
1.0 |
Zeolite (anhydr.) |
38.0 |
Water bound with zeolite |
10.84 |
Sodium silicate |
4.0 |
Acrylate/maleate copolymer |
2.0 |
Minor ingredients |
2.0 |
Sodium carbonate |
10.0 |
|
94.64 |
[0048] The ratio of zeolite (anhydrous) to non-soap surfactant in this composition is 1.46.
[0049] 35 kg of this spray-dried powder are introduced into a Fukae (Trade Mark) FS-G series
high speed mixer, and pulverised at high speed for 2-4 minutes. Water (2.0 parts)
is then sprayed in while the mixer is allowed to run at a slower speed, then the speed
is increased for 5-8 minutes while maintaining the temperature at about 35°C. During
this period granulation occurs.
[0050] A sample of the granular product is removed from the mixer. It is generally free-flowing
and shows no tendency to cake. Its dynamic flow rate can for example be about 65 ml/s.
[0051] 1.0 part of Alusil (Trade Mark) fine amorphous sodium aluminosilicate is introduced
into the Fukae mixer, which is then operated at a slow speed for 1 minute. The resulting
granular product is free-flowing and generally shows no tendency to cake. In representative
runs, its bulk density can be about 740 g/litre, its mean particle size about 405
microns and its dynamic flow rate about 105 ml/s.
[0052] The following ingredients are then mixed with the granular material to give 99 parts
of final detergent powder:
Coloured speckles |
1.5 parts |
Alcalase (TM)) |
0.61 parts |
Lipase to required extent eg |
0.5 parts |
Perfume |
0.25 parts |
[0053] (Lipase enzyme is postdosed to the required extent after the main body of preparative
steps described).
Examples 2 and 3
[0054] 35 kg of the spray-dried powder used in Example 1 are introduced into a Lödige (Trade
Mark) FM series high speed mixer, and pulverised for 4 minutes. Water (1.1 kg, 3.5%)
is then sprayed in while the mixer continues to run at the same speed, then the mixer
is allowed to run for a further 3 minutes while the temperature was maintained at
about 35°C. During this period granulation occurs. A sample (Example 2) is removed
from the mixer and its powder properties determined: these are for examples as shown
in Table 1 below.
[0055] Alusil (Trade Mark) finely divided amorphous sodium aluminosilicate (1.2 kg) is then
introduced into the mixer which is allowed to run for a further 0.5 minutes. Physical
properties of an example of the resulting powder (Example 3) are shown in Table 1
below, from which the beneficial effect on flow and bulk density of adding a flow
aid after granulation is complete is apparent. The presence of the Alusil did result
in an increase in the content of fine particles < 180 microns, but not to an unacceptable
level.
Table 1
Example |
2 |
3 |
Bulk density (g/l) |
680 |
754 |
Dynamic flow rate (ml/s) |
100 |
109 |
Particle size (microns) |
573 |
524 |
Fines content (wt% of particles < 180 microns) |
0 |
15 |
Examples 4 to 6
[0056] Three powders are prepared by spray-drying the nominal composition shown in Example
1 to three different moisture contents, as shown in Table 2 below. Since the 38.0
parts of zeolite (anhydrous basis) in the formulation require 10.84 parts of water
of hydration, the free moisture content of each powder is found by subtracting that
figure from the total moisture content: it will be noted that the powder of Example
4 is overdried, while that of Example 6 contains 3.16 parts of free moisture.
[0057] A 10 kg batch of each powder is granulated (and, where necessary, pulverised) in
a Diosna (Trade Mark) V series mixer, using an agitator speed of 196 r p m and a chopper
speed of 3000 r p m. In the case of Examples 4 and 5, where pulverisation initially
occurred, water is sprayed into the mixer, in the amount and for the time indicated,
before granulating. After granulation is complete, Alusil finely divided amorphous
sodium aluminosilicate (0.1 kg) is admixed to the granulate. Lipase enzyme is postdosed
to the required extent (e.g. 0.5%) after the main body of preparative steps described.
Properties of examples of the three granulates are shown in Table 2.
Table 2
Example |
4 |
5 |
6 |
Total moisture |
(wt %) |
8.0 |
11.0 |
14.0 |
Pulverisation |
time (min) |
4 |
3 |
- |
Water addition: |
amount (kg) |
0.2 |
0.1 |
- |
time (min) |
2 |
1 |
- |
Granulation |
time (min) |
4 |
3 |
4 |
Bulk density |
(g/l) |
740 |
832 |
735 |
Dynamic flow |
rate (ml/s) |
114 |
120 |
120 |
Compressibility |
(% v/v) |
8.8 |
9.4 |
8.8 |
Particle size |
(microns) |
483 |
553 |
521 |
Fines content (wt% < 180 microns) |
5.0 |
2.4 |
6.1 |
Example 7
[0058] The effectiveness of lipolytic enzyme in a detergent composition of the type described
above, and the comparative effectiveness of lipolytic enzyme in a comparative detergent
formulation, was estimated as follows.
(a) Triolein-soiled cotton and polyester materials were washed in a pH-stat under
uniform conditions using two detergent formulations as given below.
(b) pH-stat titration of the acidity developed by free fatty acid (FFA) during the
wash was carried out to show an index quantity of free fatty acid per standard test
cloth indicating the relative effectiveness of lipolytic action.
[0059] The detergent formulations were as follows:
|
(a) |
(b) |
|
% |
% |
linear alkylbenzene sulphonate |
20 |
26 |
coco-PAS |
- |
8 |
nonionic detergent |
2 |
4 |
soap |
1 |
3 |
zeolite (anhydrous) |
35 |
18 |
polymer |
1.5 |
1 |
sodium carbonate |
10 |
20 |
sodium sulphate |
11 |
4 |
sodium silicate |
4 |
6 |
sodium carboxymethylcellulose |
0.75 |
- |
sodium succinate |
2 |
- |
ratio b1:a |
1.59 |
0.47 |
[0060] Lipase was used in each case in an amount corresponding to 5 LU/ml wash solution,
and the wash water had 4 degrees FH Calcium, 2 degrees FH magnesium. Wash temperature
was 30 degrees C. Cloth:liquor ratio was 1:80, the cotton was soiled with 6.4% by
weight triolein and the polyester had 10% by weight triolein.
[0061] After washing with formulation (a) the test showed the presence of 2.3 micromoles
of FFA produced in the wash liquor per cotton test cloth and 7.6 micromoles of FFA
per polyester test cloth.
[0062] After washing with comparative formulation (b) the test showed the presence of 1.0
micromoles of FFA produced in the wash liquor per cotton test cloth and 6.1 micromoles
of FFA per polyester test cloth.
[0063] It was apparent that formulation (a) enabled comparatively more lipolytic activity
from the given quantity of lipolytic enzyme.
Example 8
[0064] A preferred detergent composition was prepared substantially according to the method
of Example 1 but with the following composition:
|
% by weight |
Linear alkylbenzene sulphonate |
25 |
Nonionic surfactant (7EO) |
2 |
Soap (fully hardened tallow soap) |
1 |
Zeolite (anhydr.) |
36 |
Water bound with zeolite |
10 |
Alkaline sodium silicate |
4 |
Acrylate/maleate copolymer CP5 |
1 |
Sodium carbonate |
16 |
Sodium sulphate |
2 |
Na caroxymethylcellulose |
1 |
Enzymes |
0.6 |
Minors and water |
to 100 |
[0065] The lipase (preferably Lipolase) is added as described above, and is preferably present
in addition to protease (Alcalase).
[0066] The invention is susceptible of modifications and variations within the scope of
the preceding disclosure with Examples, and extends to all combinations and subcombinations
of the features mentioned or incorporated.