Field of the invention
[0001] This invention relates to detergent compositions in the form of tablets for example,
for use in fabric washing or machine dishwashing.
Background to the invention
[0002] Detergent compositions in tablet form have advantages over powdered products in that
they do not require measuring and are thus easier to handle and dispense into the
wash-load.
[0003] Tablets comprising two or more separate regions have been described. For example
WO 01/42416 describes the production of multi-phase moulded bodies comprising a combination of
core moulded bodies and a particulate premix.
WO 00/61717 describes a detergent tablet which is characterised in that at least part of its
outer surface is semi-solid.
WO 00/04129 describes a multi-phase detergent tablet comprising a first phase in the form of
a shaped body having at least one mould therein and a second phase in the form of
a particulate solid compressed within said mould. Recently it has been suggested,
for example in
EP 1,371,729,
EP 1,405,900,
EP 1,382,368,
EP 1,375,636,
EP 1,405,901,
EP 1,405,902,
EP 1,418,224 and
WO 03/104380 to prepare tablets comprising a smooth or semi-solid phase optionally in combination
with a solid phase.
[0004] DE19925503 descibes a detergent tablet comprising at least one phase of compacted material and
at least one smooth phase, wherein the detergent tablet comprises at least one functional
substance, wherein the functional substance is an optical brightener.
Summary of the invention
[0005] An object of the present invention is to provide detergent tablets which contain
ant least one functional substance. Another object is to obtain tablets that may be
prepared in a robust production process. Still a further object is to provide such
tablets having an improved appearance. One or more of these objects are attained by
the invention.
[0006] Accordingly in a first aspect the present invention therefore provides a detergent
tablet comprising at least one compressed phase of compacted particulate material
and at least one smooth phase, wherein the detergent tablet comprises at least one
functional substance having functionality in the washing process and/or in the detergent
tablet, characterised in that the functional substance is included in the smooth phase
in such an amount that the appearance of the smooth phase is notably different from
a tablet with a smooth phase without the functional substance.
[0007] Preferably the functional substance is one or more substances chosen from the group
consisting of opacifiers, fluorescers, pearlescents, sequestrants and antifoam agents.
Detailed description of the invention
[0008] Weight percentages (wt%) herein are calculated based upon total weight of the tablet,
unless otherwise indicated.
[0009] Preferably tablets of the invention are of cylindrical shape (e.g. round, rectangular
or square) wherein the two main surfaces (upper side and bottom side) are substantially
flat.
[0010] The detergent tablet according to the invention comprises at least one (first)compressed
phase of a compacted particulate material and at least one smooth phase. Optionally
other phases may be present.
[0011] The regions or phases of a multi-phase tablet are preferably separate layers within
a detergent tablet. However, a discrete region of a tablet could also have other forms
for example one or more core(s) or insert(s).
[0012] The phases and the other characteristics of tablets according to the invention will
now be described in more detail.
Compressed phase (1st phase)
[0013] The compressed phase is a phase or region formed by compacting particulate starting
material. Preferably the compressed phase is a solid phase.
[0014] In laundry tablets, the particulate starting material of the compacted phase has
a dual function, i.e. it carries liquid like surfactants such as LAS and nonionic
and it acts as a binder to give the compacted phase sufficient hardness to survive
supply chain and consumer handling. The starting particulate material is preferably
made by granulating detergent ingredients to form a powder (base powder) to which
other detergent ingredients may be added after granulation (postdosed).
[0015] Preferably the particulate material has a mean particle size in the range from 200
to 2000 µm, more preferably from 250 to 1400 µm. Fine particles, smaller than 180
µm or 200 µm may be eliminated by sieving before tableting, if desired, although we
have observed that this is not always essential.
[0016] While the starting particulate material may in principle have any bulk density, the
present invention is especially relevant to tablets made by compacting powders of
relatively high bulk density, because of their greater tendency to exhibit disintegration
and dispersion problems. Such tablets have the advantage that, as compared with a
tablet derived from a low bulk density powder, a given dose of composition can be
presented as a smaller tablet.
[0017] Thus the starting particulate composition may suitably have a bulk density of at
least 400 g/litre, preferably at least 500 g/litre, and perhaps at least 600 g/litre.
gramsgramsgrams
[0018] Although the compacted phase may comprise surfactant materials, when the tablet comprises
also a smooth phase, then the compacted phase preferably comprises substantially no
surfactants, but ingredients other than surfactants. Examples of these ingredients
are for example builders, bleach system, enzymes etc. Preferably the builders in the
tablet are predominantly present in compacted phase. Preferably also the bleach system
is predominantly present in the compacted phase. Preferably the enzymes are predominantly
present in the compacted phase.
[0019] For the purpose of this invention, unless stated otherwise, the term "predominantly
present" refers to a situation wherein at least 90 %wt of an ingredient is present
in the third region, more preferred more than 98 %wt, most preferred substantially
100 %wt.
[0020] The compacted phase is preferably present as a distinctive region preferably having
a weight of 60-95wt%, more preferably 70-80wt%, most preferably about 77wt% of tablet
weight.
Smooth phase (2nd phase)
[0021] According to the invention, the detergent tablet comprises a smooth phase, which
comprises a functional substance.
[0022] For the purpose of this invention the term smooth phase refers to compositions which
are on the one hand solid enough to retain their shape at ambient temperature and
on the other hand smooth in appearance. Smooth textures are generally of low or no
porosity and have -at normal viewing distance- the appearance of a continuous phase
for example as opposed to porous and particulate appearance of a compacted particulate
material.
[0023] A functional substance is herein defined as a substance that has functionality in
the tablet or in the wash. Preferably the functional substance has functionality in
the wash.
[0024] Preferably the functional substance is one or more substances chosen from the group
consisting of opacifiers, fluorescers, pearlescents, water-soluble dyes, sequestrants
and antifoam agents.
[0025] A preferred functional substance is a fluorescer (optical brightener), for example,
Tinopal (Trade Mark) DMS or Tinopal CBS available from Ciba-Geigy AG, Basel, Switzerland.
Tinopal DMS is disodium 4,4'bis-(2-morpholino-4-anilino-s-triazin-6-ylamino) stilbene
disulphonate; and Tinopal CBS is disodium 2,2'-bis-(phenyl-styryl) disulphonate.
[0026] Another preferred functional substance is an anti-foam agent. An antifoam agent is
advantageously included, especially if a detergent tablet is primarily intended for
use in front-loading drum-type automatic washing machines. Suitable antifoam materials
are usually in granular form, such as those described in
EP 266863A (Unilever). Such antifoam granules typically comprise a mixture of silicone oil,
petroleum jelly, hydrophobic silica and alkyl phosphate as antifoam active material,
absorbed onto a porous absorbed water-soluble carbonate-based inorganic carrier material.
Antifoam granules may be present in an amount up to 5% by weight of the composition.
The addition of antifoam agent to the smooth phase has the advantage that the antifoam
agent is in that phase of the tablet that usually contains the major part of the surfactants
that cause foaming (such as LAS and non-ionics).
[0027] Another preferred functional substance is a pearlescent. Preferred pearlescents are
beeswax, triacontanyl palmitate, octadecyl octadecanoate , dodecyl hexadecanoate,
cetyl palmitate, lanolin, canauba wax, glycol disteatate and jojaba oil. These materials
form tiny flakes that give a pearlescent effect (the tiny flakes reflect the light).
When a pearlescent is used, the smooth phase preferably should not contain any ingredients
that substantially reduce the transparency or translucency of the smooth phase.
[0028] Another preferred functional substance is an opacifier. An opacifier will change
the light diffraction characteristic of the smooth phase. Suitable opacifiers are
metal oxides and metal hydroxides, such as aluminium hydroxide, aluminium oxide, antimony
oxide, titanium oxide. The colour of the opacifier may be used to give the smooth
layer a specific colour. Most preferred opacifier is titanium dioxide (which is white).
[0029] Especially preferred as functional substance is a mixture of opacifier and fluorescer,
more preferably titanium dioxide and fluorescer, most preferably about 0.4wt% titanium
dioxide and 0.5 wt% CBS X (fluorescer in 33wt% slurry in water). This preferred embodiment
makes it possible to prepare a tablet of one color (Smooth layer and compressed layer
have the same color, e.g. white) but still with different appearance of the layers.
In consumer tests such a tablet was especially attractive to the consumer because
of the bright white appearance of the smooth layer. Additionally, the color could
be used to identify the type of laundry tablet according to the invention (e.g. blue
for bleach containing tablets).
[0030] Preferably the functional substance is heat stable. Heat stable herein means that
the functional substance is able to withstand the temperatures used in the preparation
of the smooth phase, e.g. about 80°C, for relatively long times, e.g. several days,
without substantial decomposition.
[0031] Preferably the functional substance added to the other smooth phase ingredients as
a liquid substance. This is advantageous for dispersion of the functional substance
in the other ingredients. For this reason functional substances that are available
in liquid form are preferred.
[0032] The preferred amounts of the functional substance (based on weight of the smooth
phase) is described hereunder in table 1:
Table 1: Preferred functional substances
Functional Substance |
Examples |
Preferred amount (on smooth phase) (wt.%) |
More preferred amount (wt.%) |
Opacifier |
Titanium dioxide Acusol® |
0.01-2 |
0.1-0.8 |
Fluorescer |
CBS and Tinopal® ex Ciba |
0.1-10 |
1-5 |
Sequestrant |
Phosphonates, e.g. Dequest® ex Solutia |
0.1-10 |
1-5 |
Antifoam agent |
Silicone antifoam agents |
0.1-10 |
1-5 |
Pearlescent |
Lanolin |
0.01-2 |
0.1-0.8 |
Gas |
Air |
0.1-10 vol% |
1-5 vol% |
[0033] Preferably the functional substance is included in a smooth phase which itself is
transparent or translucent. Preferably, this means that the composition (without the
functional substance) has an optical transmissivity of at least 10%, most preferably
20%, still more preferably 30%, through a path length of 0.5 cm at 25° C. These measurements
may be obtained using a Perkin Elmer UV/VIS Spectrometer Lambda 12 or a Brinkman PC801
Colorimeter at a wavelength of 520nm, using water as the 100% standard.
[0034] By the addition of functional substance, the originally transparent starting material
may loose its transparency, since the mixture may become a dispersion. Nevertheless,
in most cases it may be possible to detect e.g. by microscopy, that despite the addition
of the functional substance, in the smooth phase still transparent or translucent
regions, i.e. the continuous phase of the dispersion, are present.
[0035] By controlling the addition of the functional substance to the smooth layer, especially
the type of the functional substance and the amount added, and optionally the addition
of colour, e.g. water-soluble dye, a broad range of different appearances of the smooth
layer is attainable according to the invention. For instance it is possible by the
addition of opacifiers and water-soluble dye to produce smooth layers with pastel
colours.
[0036] Another advantage of the controlled addition of the functional substance is that
the process for preparation of the tablets with a smooth phase becomes more robust.
In the preparation of the mixture for preparing the smooth phase, the smooth phase
ingredients are mixed and heated to relatively high temperature, e.g. to 80°C. Usually
the mixture is made in bulk and kept at this high temperature, so that the mixture
should be temperature stable for several days. Some thermal breakdown of ingredients
in the mixture will lead to slight discoloration of the smooth phase, in particular
with transparant smooth phases. Especially when process irregularities occur, often
a very light brown or yellow discolouration is observed.
[0037] We have found that by the controlled addition of functional substance according to
the invention the discolouration may be overcome in a controlled way, and accordingly
the process for preparation of the smooth phase is more robust.
[0038] Other ingredients which may be included in the smooth phase are as follows.
[0039] The smooth region of the tablet may also contain diluent materials for example polyethyleneglycol,
dipropyleneglycol, isopropanol or (mono-)propyleneglycol. Preferable the level of
these diluents is from 0 to 40 %wt, more preferred 1 to 20, most preferred from 4
to 15 %wt based on the weight of the smooth phase.
[0040] The smooth phase preferably comprises no or only low levels of water. Preferably
the level of water is less than 20 wt % based on the weight of the smooth phase, more
preferred less than 15 wt%, most preferred from 5 to 12 wt%. Most preferably the smooth
phases are substantially free from water, which means that apart from low levels of
moisture (e.g. for neutralisation or as crystal water) no additional added water is
present.
[0041] In an advantageous embodiment of the invention the smooth phase comprises from 30-100
%wt of non-soap surfactants, more preferred 40 to 90 %wt (based on the total weight
of said smooth phase), more preferred from 50 to 80 %wt. It has been found that the
combination of a separate smooth first region and these high non-soap surfactant levels
provide very good dispersing and cleaning properties to the tablet.
[0042] The smooth region advantageously comprises 50-100 %wt of non-soap surfactants for
examples 60 to 90 %wt in combination with optional ingredients such as to 0 to 50
wt% soluble materials (as described above) 0 to 40 wt% diluent materials (as described
above) and 0 to 20 wt% (as described above) of water.
[0043] The non-soap surfactants in said smooth phase may for example be anionic, nonionic
or cationic non-soap surfactants or mixtures thereof. Relatively low levels of soap
may also be present, for example up to 10 %wt based on said third smooth phase.
[0044] Preferably the total weight of surfactants in the smooth phase is from 2 to 20 grams,
more preferred from 3 to 10 grams.
[0045] The smooth phase is preferably present as a distinctive region having a weight of
5-30wt.%, more preferably 10-20wt%, most preferably about 16wt% of the tablet weight.
Other phases
[0046] Optionally the tablets according to the invention may comprise other phases then
those described above.
[0047] In a preferred embodiment, the tablets comprise a barrier phase which separates the
1
st compressed phase and the 2
nd smooth phase, which forms a barrier between the 1
st and the 2
nd phase.
[0048] The barrier phase may be prepared by any suitable method e.g. mixing, casting, spraying
etc. In a preferred method said barrier phase is obtained from the compression of
particles comprising at least 10wt% of a deformable material. Such particles preferably
comprise at least 10 %wt, more preferably at least 50%wt (based on the particles)
of the plastically deformable materials.
[0049] For the purpose of the invention the term plastically deformable material refers
to any material which on the one hand can exist in a particulate form at ambient temperatures
of say 15 to 25°C and preferably somewhat above, but which under moderate pressure
of say from 0.1 to 10, especially from 0.2 to 2 kN/cm
2 can merge or flow together when subjected to the compaction pressure.
[0050] Preferably the plastically deformable material has a softening or melting temperature
above ambient, conveniently above 35°C, better at least 40°C, Preferably the melting
temperature does not exceed 80°C, or even 70°C. Also preferably the plastically deformable
materials are water-soluble. A solubility of at least 10g per 100g deionized water
at 20°C is desirable. A higher solubility, such as at least 20g per 100 g, is preferred.
[0051] Preferred plastically deformable materials are for example organic polymers containing
polar groups, especially polyethylene glycol (PEG). Polyethylene glycols of molecular
weight from 1000 to 10,000 and above have been found suitable, especially those of
molecular weight in a range from 1000 to 5000. Other plastically deformable organic
polymers with a high proportion of hydrophilic groups could be employed. Possibilities
are polyacrylates and polyvinyl pyrrolidone. The plastically deformable material may
have surfactant properties for example nonionic surfactants containing an average
of 20 or more (preferably 30 or more) ethylene oxide residues, anionic surfactants
for example particles of linear alkyl benzyl sulphonate and soap particles.
[0052] Preferably the level of plastically deformable material in the barrier phase is from
10 to 90 wt%, more preferred from 20 to 85 wt%, most preferred from 30 to 70 wt% based
on the weight of the barrier phase.
[0053] According to a preferred embodiment the starting material of the barrier layer is
a high amphiphilic material, such as surfactants, fatty alcohols, fatty acids, fatty
amides, or fatty esters. Preferably the amphiphilic materials comprise hydrocarbon
chain(s), particularly saturated, of length of 7 carbon atoms or more, preferably
10 carbon atoms or more.
[0054] The barrier phase thus may advantageously be a soap rich phase. Such soap rich barrier
phase is hereafter described in more detail.
[0055] For the purpose of the invention the term soap rich phase refers to a separate part
of the tablet, e.g. a region, such as a layer, wherein the level of soap is at least
10% wt, more preferably at least 15% wt, still more preferably at least 20% wt, yet
more preferably at least 25% wt. Typical soap levels in the soap rich phase are from
15% to 50% by weight, more preferably from 25% to 40% by weight. However, preferably
the soap level is at least 50% wt and can even be very high say more than 80wt% or
even more than 90 %wt up to 100 %wt based on the weight of the soap rich phase. Other
ingredients may also be present in the soap rich layer, although preferably the soap
rich layer is substantially free of non-soap surfactants, bleach ingredients and builder
materials. Sometimes it may be advantageous however to incorporate into the soap rich
layer a highly soluble material such as sugars, urea, alkali metal salts such as sodium
chloride etc. Typically such highly soluble materials will have a solubility of at
least 100 grams per litre water of 20°C, more preferred at least 250 grams. Advantageously
the level of these highly soluble materials in the soap rich phase is less than 50%wt,
for example from 5 to 45 %wt, advantageously from 10 to 40 %wt.
[0056] The soap rich region of the tablet may be prepared by any suitable method for example
the spraying, applying or brushing of a soap rich formulation, if appropriate followed
by hardening e.g. by cooling. In a preferred method the soap rich layer is obtained
from the compression of soap rich particles. Such detergent particles preferably comprise
at least 10 %wt, more preferably at least 50%wt (based on the particles) of soap surfactants.
Suitable detergent particles may for example be granules or other particles having
high soap levels, for example soap noodles, marumes or granulates with high soap levels.
[0057] Preferably the level of soap surfactants in the soap rich particles is more than
50 %wt, more preferred more than 70 %wt, especially preferred from 75 %wt to 100 %wt.
Preferably the level of soap rich particles in the soap rich phase is at least 60
wt%, more preferred from 80 to 100 wt%.
[0058] Further surfactants, for example anionic, nonionic or cationic surfactants may equally
be present in the soap rich phase for example at a level of 0.1 to 10 %wt based on
the weight of the soap rich part. However normally the first soap rich phase will
be substantially free from non-soap surfactants.
[0059] In addition to the soap surfactants the soap rich region may comprise other materials
for example soluble materials such as electrolyte materials, meltable organic materials
and sugars, at a level of 2 to 70 %wt based on the weight of the smooth part, more
preferred from 3 to 50 %wt, most preferred 5 to 40 wt%. Examples of preferred materials
are water-soluble materials such as the sodium and potassium citrates, sodium chloride,
acetates and carbonates, urea and sugar. The water solubility at 20°C of these materials
is preferably at least 10 grams per 100 ml of water, more preferred more than 15 grams,
most preferably more than 20 grams.
[0060] If these soluble materials are present, their particle size is preferably chosen
such that the soap rich phase is a soap rich continuous matrix having dispersed therein
particles of the water soluble material.
[0061] It has been found that these materials provide good dissolution properties to the
soap rich phase. Furthermore these materials do not negatively affect the desired
firm consistency of the soap rich phase.
[0062] The barrier phase is preferably present as a distinctive region preferably having
a weight of 1-12wt%, more preferably 3-9wt%, most preferably about 6 wt% of tablet
weight.
[0063] The above description of the tablet has been given with reference to a tablet constituted
three or four regions. It will however be understood that each of the regions may
be composed of a limited number of discrete regions.
Similarly the smooth second region or the solid third region may composed of a limited
number (say 1-5) of parts e.g. separate layers in the tablet.
[0064] Preferably tablets of the invention are of cylindrical shape (e.g. round, rectangular
or square) wherein the two main surfaces (upper side and bottom side) are substantially
flat.
[0065] Detergent tablets according to the invention are preferably manufactured by a process
involving the application of pressure to a particulate mixture to form the first phase.
Advantageously the preparation of the first phase may involve the dosing of a particulate
mixture, followed by the exertion of moderate pressure, preferably above the yield
stress of the particles.
[0066] A multi-phase tablet comprising a first may advantageously be made by a process,
comprising the steps of:
- a) a particulate detergent composition is compacted to form a compressed phase;
- b) a barrier layer is formed on the compacted phase;
- c) a smooth layer is formed on the barrier layer
[0067] In a preferred embodiment of the invention the first particulate composition is pre-compressed
at a force of 0.1 to 20 kN/cm
2 between steps (a) and (b). In another preferred embodiment, the particulate composition
is flattened between steps (a) and (b).
[0068] Preferably the (co-) compression of the combination of the first and the solid region(s)
takes place at a force of from 0.05 to 20 kN/cm
2. Especially if the solid region has been pre-compressed the co-compression in step
(c) can advantageously be at a force of 0.1- 10 kN/cm
2, more preferred 0.5 to 5 kN/cm
2. If the solid region has not been pre-compressed, the co-compression preferably takes
place at a force of 0.5- 100 kN/cm
2, more preferred 0.7-50 kN/cm
2, most preferred 1-10 kN/cm
2.
[0069] Separately prepared phases can then be adhered to other parts of the tablet for example
by gentle pressing or by usage of an adhesive material.
[0070] Similarly a separately prepared solid phase e.g. of compressed particulate materials
can be combined with one or more pre-prepared phases e.g. by gentle co-compression.
[0071] A tablet of this invention may be intended for use in machine dishwashing. Such tablets
will typically contain salts, such as over 60 wt% of the tablet.
[0072] Water soluble salts typically used in machine dishwashing compositions are phosphates
(including condensed phosphates) carbonates and silicates, generally as alkali metal
salts. Water soluble alkali metal salts selected from phosphates, carbonates and silicates
may provide 60 wt% or more of a dishwashing composition.
[0073] Another preferred possibility is that a tablet of this invention will be intended
for fabric washing. In this event the tablet will be likely to contain at least 2
wt%, probably at least 5 wt%, up to 40 or 50 wt% soap surfactant based on the whole
tablet, and from 5 to 80 wt% detergency builder, based on the whole tablet.
[0074] Optionally, the tablets according to the invention may be fabric conditioner or fabric
softener tablets. Fabric conditioner tablets be based on for instance quaternary ammonium
type softeners and/or clays. They are described for instance in
WO0181521. In such fabric softener tablets according to the invention preferably the
[0075] Materials which may be used in tablets of this invention will now be discussed in
more detail.
Surfactant Compounds
[0076] Compositions which are used in tablets of the invention will contain one or more
detergent surfactants. In a fabric washing composition, these preferably provide from
5 to 50% by weight of the overall tablet composition, more preferably from 8 or 9%
by weight of the overall composition up to 40% or 50% by weight. Surfactant may be
anionic (soap or soap), cationic, zwitter-ionic, amphoteric, nonionic or a combination
of these.
[0077] Anionic surfactant may be present in an amount from 0.5 to 50% by weight, preferably
from 2% or 4% up to 30% or 40% by weight of the tablet composition.
[0078] Synthetic (i.e. non-soap) anionic surfactants are well known to those skilled in
the art. Examples include alkylbenzene sulphonates, particularly sodium linear alkylbenzene
sulphonates having an alkyl chain length of C
8-C
15; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates; and fatty acid
ester sulphonates.
[0079] Primary alkyl sulphate 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. 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.
[0080] Frequently, such linear alkyl benzene sulphonate or primary alkyl sulphate of the
formula above, or a mixture thereof will be the desired anionic surfactant and may
provide 75 to 100 wt% of any anionic soap surfactant in the composition.
[0081] In some forms of this invention the amount of non-soap anionic surfactant lies in
a range from 5 to 20 wt% of the tablet composition.
[0082] Soaps for use in accordance to the invention are preferably alkali metal or alkaline
earth metal salts of naturally occuring fatty acids, preferably sodium soaps derived
from naturally occurring fatty acids, for example, the fatty acids from coconut oil,
beef tallow, sunflower or hardened rapeseed oil. Especially preferably soaps are selected
from C
10 to C
20 soaps for example from C
16 to C
18 or C
12 soaps.
[0083] 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.
[0084] Specific nonionic surfactant compounds are alkyl (C
8-22) phenol-ethylene 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.
[0085] 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.
[0086] In some fabric washing tablets of this invention, the amount of nonionic surfactant
lies in a range from 4 to 40%, better 4 or 5 to 30% by weight of the whole tablet.
[0087] Many nonionic surfactants are liquids. These may be absorbed onto particles of the
composition.
[0088] In a machine dishwashing tablet the surfactant may be wholy nonionic, in an amount
below 5 wt% of the whole tablet although it is known to include some anionic surfactant
and to use up to 10 wt% surfactant in total.
Detergency Builder
[0089] A composition which is used in tablets of the invention will usually contain from
5 to 80%, more usually 15 to 60% by weight of detergency builder. This may be provided
wholly by water soluble materials, or may be provided in large part or even entirely
by water-insoluble material with water-softening properties. Water-insoluble detergency
builder may be present as 5 to 80 wt%, better 5 to 60 wt% of the composition.
[0090] Alkali metal aluminosilicates are strongly favoured as environmentally acceptable
water-insoluble builders for fabric washing. Alkali metal (preferably sodium) aluminosilicates
may be either crystalline or amorphous or mixtures thereof, having the general formula:
0.8 - 1.5 Na
2O.Al
2O
3. 0.8 - 6 SiO
2. xH
2O
[0091] These materials contain some bound water (indicated as "xH2O") and are required to
have a calcium ion exchange capacity of at least 50 mg CaO/g. The preferred sodium
aluminosilicates contain 1.5-3.5 SiO
2 units (in the formula above). Both the amorphous and the crystalline materials can
be prepared readily by reaction between sodium silicate and sodium aluminate, as amply
described in the literature. Suitable crystalline sodium aluminosilicate ion-exchange
detergency builders are described, for example, in
GB 1429143 (Procter & Gamble). The preferred sodium aluminosilicates of this type are the well
known commercially available zeolites A and X, the novel zeolite P described and claimed
in
EP 384070 (Unilever) and mixtures thereof.
[0092] Conceivably a water-insoluble detergency builder could be a layered sodium silicate
as described in
US 4664839.
[0093] NaSKS-6 is the trademark for a crystalline layered silicate marketed by Hoechst (commonly
abbreviated as □SKS-6"). NaSKS-6 has the delta-Na
2SiO
5 morphology form of layered silicate. It can be prepared by methods such as described
in
DE-A-3,417,649 and
DE-A-3,742,043. Other such layered silicates, such as those having the general formula NaMSi
xO
2x+1.yH
2O wherein M is sodium or hydrogen, x is a number from 1.9 to 4, preferably 2, and
y is a number from 0 to 20, preferably 0 can be used.
[0094] Water-soluble phosphorous-containing inorganic detergency builders, include the alkali-metal
orthophosphates, metaphosphates, pyrophosphates and polyphosphates. Specific examples
of inorganic phosphate builders include sodium and potassium tripolyphosphates, orthophosphates
and hexametaphosphates.
[0095] Non-phosphorous water-soluble builders may be organic or inorganic. Inorganic builders
that may be present include alkali metal (generally sodium) carbonate; while organic
builders include polycarboxylate polymers, such as polyacrylates, acrylic/maleic copolymers,
and acrylic phosphonates, monomeric polycarboxylates such as citrates, gluconates,
oxydisuccinates, glycerol mono- di- and trisuccinates, carboxymethyloxysuccinates,
carboxymethyloxymalonates, dipicolinates and hydroxyethyliminodiacetates.
[0096] At least one region (preferably the second region) of a fabric washing tablet preferably
include polycarboxylate polymers, more especially polyacrylates and acrylic/maleic
copolymers which can function as builders and also inhibit unwanted deposition onto
fabric from the wash liquor.
Bleach System
[0097] Tablets according to the invention may contain a bleach system in at least one region
of a tablet, preferably in the second region. This preferably comprises one or more
peroxy bleach compounds, for example, inorganic persalts or organic peroxyacids, which
may be employed in conjunction with activators to improve bleaching action at low
wash temperatures. If any peroxygen compound is present, the amount is likely to lie
in a range from 10 to 25% by weight of the composition.
[0098] Preferred inorganic persalts are sodium perborate monohydrate and tetrahydrate, and
sodium percarbonate, advantageously employed together with an activator. Bleach activators,
also referred to as bleach precursors, have been widely disclosed in the art. Preferred
examples include peracetic acid precursors, for example, tetraacetylethylene diamine
(TAED), now in widespread commercial use in conjunction with sodium perborate; and
perbenzoic acid precursors. The quaternary ammonium and phosphonium bleach activators
disclosed in
US 4751015 and
US 4818426 (Lever Brothers Company) are also of interest. Another type of bleach activator which
may be used, but which is not a bleach precursor, is a transition metal catalyst as
disclosed in
EP-A-458397,
EP-A-458398 and
EP-A-549272. A bleach system may also include a bleach stabiliser (heavy metal sequestrant) such
as ethylenediamine tetramethylene phosphonate and diethylenetriamine pentamethylene
phosphonate.
[0099] As indicated above, if a bleach is present and is a water-soluble inorganic peroxygen
bleach, the amount may well be from 10% to 25% by weight of the composition.
Other Detergent Ingredients
[0100] The detergent tablets of the invention may also contain (preferably in the second
region) one of the detergency enzymes well known in the art for their ability to degrade
and aid in the removal of various soils and stains. Suitable enzymes include the various
proteases, cellulases, lipases, amylases, and mixtures thereof, which are designed
to remove a variety of soils and stains from fabrics. Examples of suitable proteases
are Maxatase (Trade Mark), as supplied by Gist-Brocades N.V., Delft, Holland, and
Alcalase (Trade Mark), and Savinase (Trade Mark), as supplied by Novo Industri A/S,
Copenhagen, Denmark. Detergency enzymes are commonly employed in the form of granules
or marumes, optionally with a protective coating, in amount of from about 0.1% to
about 3.0% by weight of the composition; and these granules or marumes present no
problems with respect to compaction to form a tablet.
[0101] It may also be desirable that a detergent tablet of the invention includes an amount
of an alkali metal silicate, particularly sodium ortho-, meta- or disilicate. The
presence of such alkali metal silicates at levels, for example, of 0.1 to 10 wt%,
may be advantageous in providing protection against the corrosion of metal parts in
washing machines, besides providing some measure of building and giving processing
benefits in manufacture of the particulate material which is compacted into tablets.
[0102] A tablet for fabric washing will generally not contain more than 15 wt% silicate.
A tablet for machine dishwashing will often contain more than 20 wt% silicate. Preferably
the silicate is present in the second region of the tablet.
[0103] Further ingredients which can optionally be employed in a region of a fabric washing
detergent of the invention tablet (preferably the second region) include antiredeposition
agents such as sodium carboxymethylcellulose, straight-chain polyvinyl pyrrolidone
and the cellulose ethers such as methyl cellulose and ethyl hydroxyethyl cellulose,
fabric-softening agents; heavy metal sequestrants such as EDTA; perfumes; and colorants
or coloured speckles.
[0104] Further ingredients which can optionally be used in tablets of the invention, preferably
in the second region are dispersing aids. Examples of suitable dispersing aids are
water-swellable polymers (e.g. SCMC) highly soluble materials (e.g. sodium citrate,
potassium carbonate or sodium acetate) or sodium tripolyphospate with preferably at
least 40% of the anhydrous phase I form.
Particle Size and Distribution
[0105] The first soap rich region of the detergent tablet may advantageously be prepared
by compacting particles with a high soap content as described above. Preferably these
particles have a mean particle size of from 100 to 1000 µm. The second region of a
detergent tablet of this invention, is a preferably a matrix of compacted particles.
[0106] Preferably the particulate composition has a mean particle size in the range from
200 to 2000 µm, more preferably from 250 to 1400 µm. Fine particles, smaller than
180 µm or 200 µm may be eliminated by sieving before tableting, if desired, although
we have observed that this is not always essential.
[0107] While the starting particulate composition may in principle have any bulk density,
the present invention is especially relevant to tablets made by compacting powders
of relatively high bulk density, because of their greater tendency to exhibit disintegration
and dispersion problems.
[0108] Such tablets have the advantage that, as compared with a tablet derived from a low
bulk density powder, a given dose of composition can be presented as a smaller tablet.
[0109] Thus the starting particulate composition may suitably have a bulk density of at
least 400 g/litre, preferably at least 500 g/litre, and perhaps at least 600 g/litre.
[0110] Tableting machinery able to carry out the manufacture of tablets of the invention
is known, for example suitable tablet presses are available from Fette and from Korch.
[0111] Tableting may be carried out at ambient temperature or at a temperature above ambient
which may allow adequate strength to be achieved with less applied pressure during
compaction. In order to carry out the tableting at a temperature which is above ambient,
the particulate composition is preferably supplied to the tableting machinery at an
elevated temperature. This will of course supply heat to the tableting machinery,
but the machinery may be heated in some other way also.
[0112] The size of a tablet will suitably range from 10 to 160 grams, preferably from 15
to 60 g, depending on the conditions of intended use, and whether it represents a
dose for an average load in a fabric washing or dishwashing machine or a fractional
part of such a dose. The tablets may be of any shape. However, for ease of packaging
they are preferably blocks of substantially uniform cross-section, such as cylinders
or cuboids. The overall density of a tablet preferably lies in a range from 1040 or
1050gm/litre up to 1600gm/litre.
Method of manufacture
[0113] Detergent tablets according to the invention are preferably prepared by separately
preparing a (pre-)tablet of compacted powdered composition and a smooth (pre-) tablet,
followed by an assembly process to prepare the multi-phase tablet.
[0114] Accordingly in a a preferred method to prepare the detergent comprises the steps
of
- (a) Preparation of a smooth first tablet;
- (b) Compression of the particulate material to form a second compressed tablet of
compacted particulate material;
- (c) Assembling the first tablet and the second tablet.
[0115] Preferably the second tablet is manufactured by inserting a particulate composition
into a tablet mould followed by compression of the particulate composition part(s)
to form a compressed tablet.
[0116] Preferably the first tablet is manufactured by a casting process. Suitable casting
process involve the liquidising of the composition of the smooth phase for example
by heating followed by inserting the composition into mold, followed by solidification
for example by ageing or cooling.
[0117] Especially preferably the casting involves the heating of the composition of the
second tablet filling the composition into a mold and cooling.
[0118] The assembly process for combining the first and the second tablet can be any suitable
process for example the co-compression or the adhering of the two phases into one
tablet.
[0119] Preferably the diameter of the first tablet is substantially the same as the diameter
of the second tablet. For the purpose of the invention "substantially the same diameter"
means that the diameter of the first tablet differs less than 5 mm with the diameter
of the second tablet more preferably less than 3mm or even less than 1mm.
[0120] This allows for ease of assembly and resulting in a multi-phase detergent tablet
wherein each of the phases is present as a separate layer of the tablet. If appropriate
adhesive materials may be used to improve the connection between the phases of the
multi-phase detergent tablet.
[0121] The present invention will now be explained in more detail by way of the following
non-limiting examples.
Examples
Examples 1 to 3 and comparative experiment A
[0122] A detergent powder was made of the following composition:
[0123] A detergent base powder, incorporating organic surfactants, a small percentage of
crystalline sodium acetate trihydrate, and zeolite MAP was made using known granulation
technology. It had the following composition, shown as parts by weight.
Table 1
Ingredient |
Parts by Weight |
Sodium linear alkylbenzene sulphonate |
20.85 |
nonionic surfactant (C13-C15 branched fatty alcohol 3EO) |
3.07 |
nonionic surfactant (C13-15 branched fatty alcohol 7EO) |
5.98 |
Soap |
1.62 |
zeolite A24 |
46.70 |
Sodium acetate trihydrate |
5.92 |
Sodium carbonate |
6.60 |
sodium carboxymethyl cellulose (SCMC) |
0.64 |
additional moisture and minor ingredients |
8.50 |
Total |
100 |
[0124] The amount of zeolite MAP (zeolite A24) in the table above is the amount which would
be present if it was anhydrous. Its accompanying small content of moisture is included
as part of the moisture and minor ingredients. The base powder and other ingredients
were mixed together as set out in the following table 2.
Table 2
Comp A. |
Parts by Weight |
Base powder, as above |
57.18 |
Antifoam (1) |
2.30 |
Fluorescer (2) |
1.59 |
Sodium percarbonate |
19.23 |
TAED (3) |
6.48 |
Sodium disilicate |
4.07 |
Soil release polymer (4) |
1.40 |
Acrylic/maleic copolymer (5) |
1.53 |
EDTM phosphonate 0.95 Colored speckles |
1.77 |
Cellulosic swelling disintegrant (6) |
3.50 |
Total |
100.0 |
Wherein:
(1) Antifoam is 17%wt silicon oil, 71%wt sodium carbonate and the remainder petroleum
jelly and phosphate ester.
(2) Fluorescer is 9.9%wt Fluorescer and 82.5%wt sodium carbonate the remainder being
minor ingredients
(3) TAED is 83%wt TAED in 9%wt sodium sulphate the remainder being minor ingredients.
(4) Soil release polymer is 18%wt soil-release polymer, 44%wt zeolite MAP, 21%wt sodium
carbonate and minor ingredients. |
(5) Acrylic/maleic polymer is Sokolan CP5 ex BASE (91%wt active) (6) Cellulosic swelling
disintegrant (Arbocel ex Rettenmaier)
[0125] The solid phase was made by mixing the ingredients (except for the cellulosic swelling
disintegrant) and finally adding the cellulosic swelling disintegrant.
[0126] The solid phase was made in a labscale Graseby Specac tabletting press; and had a
strength (expressed in terms of the diametrical fracture stress) of approximately
25k Pa. The diametrical stress is defined as DFS=2*Fmax/(Π*D*t) with Fmax being the
tablet strength expressed as the force required to break a tablet when it is applied
on its circumference. D the tablet diameter and t its thickness.
[0127] A second exemplary solid phase formulation is exactly as for the above formulation
an except that the level of the cellulosic swelling disintegrant is to 1.75% wt (and
the base powder increased to 58.93% wt of the final formulation.
[0128] Smooth or semi-solid parts were prepared of the following composition:
Table 3
Ingredient |
Composition Parts by wt |
Na-las |
34 |
Nonionic(Lutensol AO5) |
26 |
Soap(Pristerene4916)* |
5 |
Mono propylene glycol solvent |
27 |
Water |
8 |
Notes: * is a C16-C18 soap |
Preparation of tablets of examples 1 to 3 and comparative experiment A.
[0129] The smooth phase composition of table 3 was heated to 80°C and the functional substance
(1,2,3) was added. In comparative experiment A no functional substance was added (see
table 4 for details).
Table 4
No |
Functional substance |
Amount in gel (smooth phase) (wt.%) |
Appearance of gel |
1 |
TiO2 , and |
0.4 |
Non-transparent Bright white |
Fluorescer CBS X ex Ciba (33% water slurry) |
0.5 |
2 |
TiO2 |
0.1 |
Semi-transparent With slight brownish shade |
3 |
TiO2 |
0.1 |
Semi-transparent Bright blue pastel color |
Fluorescer as Ex.1 |
0.25 |
Blue dye (BlueHP ex Milliken) |
0.025 |
A |
No functional substance |
- |
Transparent Brownish shade |
[0130] Subsequently the smooth phase composition was cast into moulds and cooled to 20°C
to form firm, 5 grammes smooth and semi-solid parts of 32mm diameter and 6mm high.
[0131] Multi-layer tablets were made by pre-compressing 25 grammes of the powdered composition
in a die of 45 mm diameter at 4 kN/cm
2, followed by adherence of a smooth and semi-solid part on top of the compressed layer
followed by a final compression step at 0.1 kN/cm
2. During the final compression step, the smooth and semi-solid part flows by the compaction
forces to form a 3.4 mm smooth semi-solid layer adhered on top of the compressed particulate
layer.