TECHNICAL FIELD
[0001] The present invention relates to a product for treating fabrics in the washing machine
in the form of a tablet containing a particulate bleaching composition which may optionally
include detergent ingredients.
BACKGROUND AND PRIOR ART
[0002] Detergent compositions in tablet form have been known for many years although the
form has never achieved great popularity on the market. In principle, tablets offer
several advantages over powder products: they do not require measuring and are thus
easier to handle and dispense into the the washload, and they are more compact, hence
facilitating more economical packaging and storage.
[0003] One difficulty that has been experienced in the formulation of detergent tablets
is the incorporation of bleaching ingredients, especially when the presence of bleach-sensitive
ingredients such as enzymes is also desired: in a compressed tablet, the ingredients
are much more intimately associated with one another than in a powder, and any adverse
interactions and instability will be exacerbated. Worse stability problems would be
expected if bleach activators (bleach precursors) were present.
[0004] US 4 099 912 (Ehrlich) discloses a plurality of separate units of different detergent
composition components which may be used in combination to obtain the required detergent
formulation. Tablets are the preferred unit. A separate tablet containing sodium perborate
or sodium percarbonate is suggested. Bleach activators are not mentioned.
[0005] GB 911 204 (Unilever) discloses layered detergent tablets containing persalt bleach,
for example, sodium perborate, and certain bleach activators, for example, sodium
acetoxybenzene sulphonate and phthalic anhydride. To avoid destabilisation, the bleach
activator is segregated from the remaining tablet ingredients, including the persalt
bleach, in a separate section or layer.
[0006] In contrast, EP 395 333A (Unilever) discloses a detergent tablet containing sodium
perborate in conjunction with one or more bleach-sensitive ingredients - tetraacetylethylenediamine
or similar bleach activator, enzyme, fluorescer, or any combination of these - as
well as detergent-active compounds, detergency builders and optionally other ingredients.
The persalt is not segregated from the bleach-sensitive ingredients but, surprisingly,
the tablet is stable with no more loss of bleach, enzyme or fluorescer performance
on storage than in a powder of the same composition.
[0007] It has now been discovered that tablets containing persalt bleaches and defined bleach
activators together, in conjunction with detergent ingredients which are either present
in the same tablet or in a separate tablet, or powder/liquid form, can give better
bleaching performance than detergent powders of the same formulation. The benefits
are especially evident when the persalt is sodium percarbonate and when the bleach
activator is tetraacetylethylenediamine.
DEFINITION OF THE INVENTION
[0008] The present invention provides a tablet of compressed particulate bleaching composition
comprising:
(i) a persalt;
(ii) a bleach activator having an observed pseudo-first order perhydrolysis rate constant
(Kobs) of from 1.5 x 10⁻⁴ to 350 x 10⁻⁴ sec⁻¹;
(iii) optionally a detergent-active compound;
(iv) optionally a detergency builder; and
(v) optionally other detergent ingredients;
with the proviso that if the persalt is sodium perborate and the bleach activator
is a N-diacylated or N,N′-polyacylated amine, the persalt is segregated from the bleach
activator.
[0009] Tablets in which sodium perborate and an N-diacylated or N,N′-polyacylated amine
bleach activator are together without segregation are disclosed and claimed in the
aforementioned EP 395 333A (Unilever) and are specifically disclaimed from the scope
of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
[0010] The tablet of the invention is characterised by the presence of both a persalt and
a defined bleach activator. The interaction between the two bleaching components,
to give better bleaching than the persalt alone can give, appears to be improved by
tabletting.
[0011] Bleach activators work by reacting in the wash liquor with hydrogen peroxide from
the persalt (perhydrolysis of the activator) to generate a peracid which is a more
efficient bleach than is hydrogen peroxide itself. Without limiting in any way the
scope of the invention, it is hypothesised that in a porous tablet there is an opportunity
for the activator to react with hydrogen peroxide from the persalt within the pores
of the tablet itself, when the tablet first comes into contact with the wash liquor.
In this confined space, the concentration of both hydrogen peroxide and precursor
will be greater than in the bulk wash liquor, and the rate of perhydrolysis will be
increased.
[0012] This can only occur, of course, if the tablet remains intact in the wash liquor for
long enough for the reaction to take place to a significant degree. However, the peracid
generated needs to be released into the wash liquor in order to reach the stain to
be bleached, which requires the tablet to dissolve. A rate of tablet dissolution that
represents an ideal compromise between these conflicting requirements is therefore
desirable. A further requirement would appear to be that the tablet should remain
porous enough under wash conditions to allow water to penetrate in sufficient quantity
and with sufficient speed for reaction to take place. Rate of dissolution and tablet
porosity will depend partly on formulation and may be also be controlled to some extent
by choice of tabletting pressure.
The persalt
[0013] The most preferred persalt for use in the present invention is sodium percarbonate,
although the use of other inorganic persalts, notably sodium perborate tetrahydrate
is also within the scope of the invention.
[0014] Sodium percarbonate, Na₂CO₃.1.5H₂O₂, unlike sodium perborate, is a perhydrate rather
than a true persalt, and it can release hydrogen peroxide of crystallisation without
requiring dissolution. However, sodium percarbonate dissolves more slowly than sodium
perborate monohydrate in water so that the tablet structure is maintained in the wash
liquor for a sufficient length of time for the effect described above to operate.
[0015] Very little benefit has been observed with sodium perborate monohydrate, which dissolves
very rapidly in water so that the tablet breaks up more quickly, but which requires
an inherently slower reaction (hydrolysis) to release hydrogen peroxide.
[0016] Some benefit has been observed with sodium perborate tetrahydrate which is slower
to dissolve than the monohydrate, but the effect is smaller than with sodium percarbonate.
[0017] The total amount of persalt in the tabletted composition as a whole is preferably
within the range of from 5 to 60 wt%. In fully formulated detergent tablets the amount
of persalt is preferably from 10 to 40 wt%, more preferably 10 to 30 wt%.
The bleach activator
[0018] The tablet of the invention also contains a defined bleach activator.
[0019] The extent to which the effect described above will operate will depend on the choice
of bleach activator as well as on the choice of persalt. Preferably the activator
is one having moderate reactivity, where the greatest improvement will be observed.
Very fast reacting bleach activators will already perform so well that no further
significant improvement is possible; while very slow reacting bleach activators will
be improved but not necessarily to a sufficient extent to render them useful in practice.
[0020] It is thus an essential feature of the present invention for the bleach activator
to have an observed pseudo-first order perhydrolysis rate constant (K
obs) of from 1.5 x 10⁻⁴ - 350 x 10⁻⁴ sec⁻¹. This rate constant provides a measure as
to how reactive the bleach activator will be.
[0021] The best known bleach activators are peracetic acid precursors and perbenzoic acid
precursors. The peracetic acid precursor, tetraacetylethylenediamine (TAED), is especially
preferred for use in the tablets of the present invention because its reactivity is
such that a particularly worthwhile improvement over loose powder can be demonstrated
(K
obs = 2.3 x 10⁻³ sec⁻¹).
[0022] The peracetic acid precursor, glycerol triacetate, has also shown some benefit, but
its reactivity is still rather low (K
obs = 1.9 x 10⁻⁴ sec⁻¹). Other peracetic acid precursors that would be expected to benefit
from tabletting in accordance with the present invention include glucose pentaacetate
and xylose tetraacetate.
[0023] An example of a perbenzoic acid precursor that may benefit from tabletting in accordance
with the present invention is sodium benzoyloxybenzene sulphonate, although since
this is already a fast-reacting precursor (K
obs = 3 x 10⁻² sec⁻¹) the benefit is less substantial than with TAED.
[0024] Further examples of suitable precursors that may benefit from tabletting in accordance
with the present invention are monosaccharide esters as disclosed in EP 0 380 437A
(Procter & Gamble; Novo), and sugar ester-based precursors as disclosed in WO91/10719
(P&G; Novo) preferred compounds are 1-O-(long-chain acyl)-2,3,4,6-tetra-O-acetyl-glucose
in α or β form where the long chain acyl is one of the following: octanoyl, nonanoyl,
decanoyl, undecanoyl, dodecanoyl, 10-undecanoyl, 3,5,5-trimethylhexanoyl or 2-ethylhexanoyl.
The most preferred compound is where the long chain acyl is octanoyl: 1-O-octanoyl-2,3,4,6-tetra-O-acetyl-glucose
(OTAG).
[0025] Bleach activators are suitably present in an amount of from 1 to 30 wt%. In fully
formulated detergent tablets the bleach activators are preferably present in an amount
of from 1 to 10 wt%, more preferably from 2 to 5 wt%.
Bleach stabiliser
[0026] If desired, the tablet of the invention may also include a small amount of a bleach
stabiliser (heavy metal sequestrant) such as ethylenediamine tetraacetate (EDTA),
ethylenediamine tetramethylene phosphonate (EDTMP) or diethylenetriamine pentamethylene
phosphonate (DTPMP).
Other ingredients
[0027] As well as persalt and bleach activator, the tablet of the invention may optionally
contain at least one detergent-active compound, at least one detergency builder, and
other ingredients. Tablets of the invention may therefore provide a fully formulated,
high performance detergent composition within a single tablet. It is preferred, however,
that a detergent composition consists of at least a two-tablet system; one, a tablet
of the invention, containing the bleaching composition, the other containing the detergent
base composition. Alternatively the detergent composition may consist of a tablet
of the invention, containing the bleaching composition, and a power/liquid containing
the detergent base composition.
Percarbonate segregation
[0028] If sodium percarbonate is present, it is preferably separated from any other ingredient
likely to destabilise it by segregation in a discrete region of the tablet, as described
and claimed in our copending British application No 90 22724.0 (Unilever PLC), filed
19 October 1990. This is particularly important when tablets which contain a full
detergent composition within a single tablet are formulated.
[0029] According to British Application No 90 22724.0, at least one discrete region comprising
sodium percarbonate and optionally other ingredients compatible with sodium percarbonate
is present. Other components such as detergent-active compound, detergency builder
and any other ingredients of doubtful compatibility with sodium percarbonate are excluded
from the discrete region(s) in which the sodium percarbonate is segregated.
[0030] A preferred embodiment of the invention which is simple in structure and simple to
manufacture is a tablet consisting of two layers: the first layer containing the percarbonate,
and the second layer containing other ingredients. The percarbonate may be segregated
alone, or together with one or more other ingredients that are fully compatible with
it. It is generally preferred that a major proportion of the non-percarbonate ingredients
should be separated from the percarbonate.
[0031] However, the stability of the percarbonate may actually be increased by segregating
it together with a diluent in the form of a compatible inorganic salt. The salt is
preferably in a finely divided or highly porous form, having a preferred surface area,
as measured using nitrogen absorption, of 5-15 m²/g. It is believed that it contributes
to percarbonate stability by acting as a moisture sink. One especially preferred inorganic
salt is sodium carbonate, which of course also plays a useful role in the detergent
composition as a whole, as a detergency builder and provider of alkalinity. It is
believed that sodium carbonate may also contribute to percarbonate stability by reabsorption
of any liberated hydrogen peroxide.
[0032] According to one especially preferred embodiment of the invention, the diluent is
in the form of a spray-dried composition comprising the compatible inorganic salt,
more preferably sodium carbonate, and a polymeric binder.
[0033] The binder must itself be stable to oxidation. Preferred binders are acrylic and/or
maleic polymers, for example, the acrylic/maleic copolymer sold commercially as Sokalan
(Trade Mark) CP5 ex BASF. As well as their binder function which improves tablet integrity
and allows tabletting without having to wet the percarbonate to any significant degree,
polycarboxylate polymers of this type also have a useful detergency building and antiredeposition
action.
[0034] In this embodiment of the invention, the discrete tablet region or layer is the compaction
product of a particulate composition prepared by mixing sodium percarbonate with the
spray-dried salt/polymeric binder granules. This particulate starting composition
suitably contains from 30 to 70 wt% of sodium percarbonate, from 30 to 70 wt% of the
inorganic salt (preferably sodium carbonate), and from 0.5 to 5 wt% of the polymeric
binder.
Detergent-active compounds
[0035] In a tablet intended to provide a fully-formulated bleaching detergent composition,
detergent-active compounds are suitably present in an amount of from 2 to 50 wt%,
more preferably from 5 to 40 wt%. Detergent-active material present may be anionic
(soap or non-soap), cationic, zwitterionic, amphoteric, nonionic, or any combination
of these.
[0036] Anionic detergent-active compounds may be present in an amount of from 2 to 40 wt%,
preferably from 4 to 30 wt%.
[0037] Synthetic 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 C₈-C₁₅; primary and secondary alkyl sulphates, particularly
sodium C₁₂-C₁₅ primary alcohol sulphates; olefin sulphonates; alkane sulphonates;
dialkyl sulphosuccinates; and fatty acid ester sulphonates.
[0038] It may also be desirable to include one or more soaps of fatty acids. These are preferably
sodium soaps derived from naturally occurring fatty acids, for example, the fatty
acids from coconut oil, beef tallow, sunflower or hardened rapeseed oil.
[0039] Anionic surfactants are preferably concentrated in discrete domains as described
and claimed in our copending British Patent Application No 90 15504.5 (Unilever PLC).
[0040] Suitable nonionic detergent 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 either alone or with propylene oxide.
[0041] Specific nonionic detergent compounds are alkyl (C₆₋₂₂) phenol-ethylene oxide condensates,
the condensation products of linear or branched aliphatic C₈₋₂₀ primary or secondary
alcohols with ethylene oxide, and products made by condensation of ethylene oxide
with the reaction products of propylene oxide and ethylenediamine. Other so-called
nonionic detergent compounds include long-chain tertiary amine oxides, tertiary phosphine
oxides, and dialkyl sulphoxides.
[0042] Especially preferred are the primary and secondary alcohol ethoxylates, especially
the C₁₂₋₁₅ primary and secondaiy alcohols ethoxylated with an average of from 5 to
20 moles of ethylene oxide per mole of alcohol.
[0043] The nonionic detergent-active compounds are preferably concentrated in discrete domains.
Since the nonionic detergent compounds are generally liquids, these domains are preferably
formed from any of the well-known carriers in the detergent business impregnated by
nonionic detergent-active compound. Preferred carriers include zeolite; zeolite granulated
with other materials, for example, Wessalith CS (Trade Mark), Wessalith CD (Trade
Mark), Vegabond GB (Trade Mark), sodium perborate monohydrate; Burkeite (spray-dried
sodium carbonate and sodium sulphate as disclosed in EP 221 776A (Unilever)).
[0044] Nonionic detergent-active compounds may optionally be mixed with materials which
make the granules slow wetting and/or prevent the nonionic leaching out into the main
tablet matrix. Such materials may suitably be fatty acids, especially lauric acid.
Detergency builders
[0045] Fully-formulated detergent tablets in accordance with the invention may suitably
contain one or more detergency builders, preferably in an amount of from 5 to 80 wt%,
more preferably from 20 to 80 wt%.
[0046] Preferred detergency builders are alkali metal aluminosilicates. However, these builders
have a particular tendency to destabilise sodium percarbonate: therefore, in tablets
of the invention containing sodium percarbonate segregation of these two components
is essential.
[0047] Alkali metal (preferably sodium) aluminosilicates may suitably be incorporated in
amounts of from 5 to 60% by weight (anhydrous Psis) of the composition, and may be
either crystalline or amorphous or mixtures thereof, having the general formula:
0.8-1.5 Na₂O. Al₂O₃.0.8-6 SiO₂
[0048] These materials contain some bound water 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
SiO₂ 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.
[0049] Suitable crystalline sodium aluminosilicate ion-exchange detergency builders are
described, for example, in 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. Also of interest is the novel zeolite P described and claimed in EP 384 070A
(Unilever).
[0050] Other builders may also be included in the detergent tablet of the invention if necessary
or desired: suitable organic or inorganic water-soluble or water-insoluble builders
will readily suggest themselves to the skilled detergent formulator. 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 phosphinates; monomeric polycarboxylates such as citrates, gluconates,
oxydisuccinates, glycerol mono-, di- and trisuccinates, carboxymethyloxysuccinates,
carboxymethyloxymalonates, dipicolinates, hydroxyethyliminodiacetates; and organic
precipitant builders such as alkyl- and alkenylmalonates and succinates, and sulphonated
fatty acid salts.
[0051] Especially preferred supplementary builders are polycarboxylate polymers, more especially
polyacrylates and acrylic/maleic copolymers, suitably used in amounts of from 0.5
to 15 wt%, especially from 1 to 10 wt%; and monomeric polycarboxylates, more especially
citric acid and its salts, suitably used in amounts of from 3 to 20 wt%, more preferably
from 5 to 15 wt%. As previously indicated, at least part of any polymer required in
the formulation may be incorporated, as binder, in the region of the tablet in which
the sodium percarbonate is segregated.
[0052] Preferred tabletted compositions of the invention preferably do not contain more
than 5 wt% of inorganic phosphate builders, and are desirably substantially free of
phosphate builders. However, phosphate-built tabletted compositions are also within
the scope of the invention.
Enzymes
[0053] Fully-formulated tablets in accordance with the invention may also contain 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. Most enzymes are bleach-sensitive to some
extent, and should also be excluded from the region containing the sodium percarbonate.
[0054] 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), Esperase (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 amounts 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.
Minor ingredients
[0055] Fully-formulated tablets in accordance with the invention may also contain 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.
[0056] An antifoam material is advantageously included in the fully-formulated tablet of
the invention, especially if the 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 266 863A (Unilever). Such antifoam granules typically
comprise a mixture of silicone oil, petroleum jelly, hydrophobic silica and alkyl
phosphate as antifoam active material, sorbed onto a porous absorbent water-soluble
carbonate-based inorganic carrier material. Antifoam granules may be present in any
amount up to 5% by weight of the composition.
[0057] It may also be desirable to include in the fully-formulated detergent tablet of the
invention an amount of an alkali metal silicate, particularly sodium ortho-, meta-
or preferably neutral or alkaline silicate. 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.
[0058] Further ingredients which can optionally be employed in the fully-formulated detergent
tablet of the invention include antiredeposition agents such as sodium carboxyethylcellulose,
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; pigments, colorants or coloured speckles; and inorganic salts
such as sodium and magnesium sulphate. Sodium sulphate may if desired be present as
a filler material in amounts up to 40% by weight of the composition; however as little
as 10% or less by weight of the composition of sodium sulphate, or even none at all,
may be present.
[0059] As well as the functional detergent ingredients listed above, there may be present
various ingredients specifically to aid tabletting or to aid tablet dispersion in
the wash, for example, binders, disintegrants, or lubricants. As already indicated,
some ingredients may give both functional wash benefits and tabletting benefits.
Tabletting
[0060] As previously indicated, the tablets of the invention are prepared by compaction
of particulate starting material. Any suitable compacting process may be used, for
example, tabletting, briquetting or extrusion, but tabletting is generally preferred.
[0061] For any given starting composition, the time taken for the tablet to disintegrate
in the wash liquor will vary with the compaction pressure used to form the tablet.
If the compaction pressure is too low, the tablet will tend to crumble and break up
in the dry state, on handling and packaging; an increase in compaction pressure will
improve tablet integrity, but eventually at the expense of disintegration time in
the wash liquor.
[0062] Using an Instron (Trade Mark) Universal Testing Machine at constant speed, or a Research
and Industrial screw hand press, to operate a steel punch and die, it has been found
that effective tablets may be produced using compaction pressures ranging from 0.1
to 500 MPa (0.01 to 50 kN/cm²), especially from 0.2 to 100 MPa (0.02 to 10 kN/cm²).
[0063] The optimum compaction pressure will depend to some extent on the starting composition;
for example, a tablet containing only the bleach composition of the invention may
require a higher compaction pressure than that required for a fully formulated detergent
composition tablet; a formulation containing a high proportion of organic ingredients
(for example, surfactants) and a low proportion of inorganic salts may require a compaction
pressure lower than that required for a formulation containing a lower proportion
of organic ingredients and a higher proportion of inorganic salts; and a dry-mixed
formulation will generally require a higher pressure than will a spray-dried powder.
Preferred tablet forms
[0064] Preferred tablets having improved disintegration and dissolution properties are described
and claimed in our copending British Patent Applications Nos 90 15503.7 and 90 15504.5
(Unilever PLC) filed on 13 July 1990, and our copending British Patent Application
filed on 1 July 1991 (Unilever PLC). These preferred tablet forms have particular
relevance for tablets of fully formulated detergent compositions.
[0065] The tablet described and claimed in Application No. 90 15503.7 or a discrete region
thereof, consists essentially of a matrix of particles substantially all of which
have a particle size within a range having upper and lower limits each lying within
the range of from 200 to 2000 µm and differing from each other by not more than 700
µm.
[0066] According to Application No. 90 15504.5, a tablet of compacted particulate detergent
composition comprises a minor proportion (2-40 wt%) of a first component (a) which
contains 20-100 wt% anionic surfactant, the rest of the composition containing only
0-3 wt% anionic surfactant.
[0067] The tablet described and claimed in our British application filed on 1 July 1991,
or a discrete region thereof, consists essentially of a matrix of particles substantially
all of while have a particle size >200µm, at least the particles of detergent-active
compound and detergent builder are coated with binder/disintegrant before tablet compaction.
Dosage forms
[0068] The tablet of the invention may provide a bleaching composition for treating fabrics
in the washing machine. This tablet may preferably be used as one of two or more tablets
within a two-tablet or multi-tablet detergent system. Especially preferred is a two-tablet
system in which the second tablet containing the detergent base system.
[0069] Alternatively, the detergent tablet of the invention may be formulated for use as
a complete heavy-duty fabric washing composition. The consumer does not need to use
a mix of tablets having different compositions.
[0070] Although one fully-formulated or bleach-only tablet may contain sufficient of all
the components to provide the correct amount required for an average washload, it
is convenient if each tablet contains a submultiple quantity of the composition required
for average washing conditions, so that the consumer may vary the dosage according
to the size and nature of the washload. For example, tablet sizes may be chosen such
that two fully-formulated or bleach-only tablets are sufficient for an average washload;
one or more further tablets may be added if the washload is particularly large or
soiled; and one only tablet may be used if the load is small or only lightly soiled.
[0071] Alternatively, larger subdivisible full-formulated or bleach-only tablets representing
a single or multiple dose may be provided with scorings or indentations to indicate
unit dose or submultiple unit dose size to the consumer and to provide a weak point
to assist the consumer in breaking the tablet if appropriate.
[0072] The size of the tablet will suitably range from 5 to 160 g, depending on the wash
conditions under which it is intended to be used; whether it is a bleach-only tablet
or contains other ingredients; and whether it represents a single dose, a multiple
dose or a submultiple dose. Bleach-only tablets preferably range from 5 to 50 g in
size. Fully formulated tablets preferably range from 10 to 160 g in size, more preferably
from 15 to 60 g in size.
[0073] The tablet may be of any suitable shape, but for manufacturing and packaging convenience
is preferably of uniform cross-section, for example, circular (preferred) or rectangular.
EXAMPLES
[0074] The following non-limiting Examples illustrate the invention. Parts and percentages
are by weight unless otherwise stated. Examples identified by numbers are in accordance
with the invention, while Examples identified by letters are comparative.
Examples 1 to 3
Measurement of the observed pseudo-first order perhydrolysis rate constant
[0075] A 4.1mM solution of sodium perborate tetrahydrate was prepared at 30°C and buffered
to pH 10 with (25mM) sodium carbonate buffer.
[0076] 2.1/n mM of activator, where n is the number of perhydrolysable groups on the activator,
was added neat (ie not in solution) to the predissolved perborate.
[0077] The peracid yields were measured using a sodium thiosulphate titration at 0°C (standard
acid/ice method).
[0078] The observed pseudo-first-order perhydrolysis rate constant (K
obs) was measured for the following activators:

Results are shown in Table 1.

Examples 4 to 6, Comparative Examples A to C
(i) Preparation of bleach compositions
[0079] A 40 wt% solution of Analar sodium carbonate was prepared. Acrylic/maleic copolymer
in sodium salt form - Sokalan (Trade Mark) CP5 ex BASF - was admixed in an amount
of 2 wt% based on the sodium carbonate (dry weight), and the solution was stirred
at 50°C for 2 hours. The solution was then spray-dried using laboratory equipment
(inlet temperature 275°C, feed rate 10 ml/min through a 0.75 mm jet) to give granular
anhydrous sodium carbonate of high specific surface area.
[0080] Bleach compositions were then prepared by dry-mixing the spray-dried sodium carbonate
composition with sodium percarbonate and bleach activator to give the formulations
shown in Table 2. The bleach activators used were TAED (in granule form), glycerol
triacetate (GTA), and sodium benzoyloxy benzenesulphonate (SBOBS), used in amounts
chosen to give equivalent weights of peracid (assuming 100% peracid generation efficiency).
The GTA, being a liquid, was preabsorbed in the spray-dried sodium carbonate.
(ii) Preparation of detergent base composition
[0081] A detergent base composition was prepared to the formulation shown in Table 2, by
spray-drying an aqueous slurry of all ingredients except the nonionic surfactant 7EO
which was subsequently sprayed on.
(iii) Tabletting
[0082] Tablets were prepared using an Instron (Trade Mark) Model 4202 Materials Testing
Machine fitted with a 10KN load cell.
[0083] For Examples 4 to 6 (the invention), bleach compositions (10 g) was added to the
die, the die was tapped gently to level the powder, and detergent base composition
(30 g) was added on top of the bleach composition, before tabletting.
[0084] The tablets each weighed 40 g, and were 53 mm in diameter and 22 mm in thickness.
[0085] Comparative Examples A, B and C were loose powders of the same composition, prepared
by mixing the bleach composition and the detergent base composition in the same proportions
as in Example 4.
(iv) Bleaching performance
[0086] Bleaching performance was assessed by measuring the increase in reflectance at 460
nm (with incident light <400 nm filtered out) (δR
460*) of standard tea-stained test cloths after washing in a Miele (Trade Mark) 756 front-loading
automatic washing machine, using a standard heat-up to 40°C wash in the presence of
a 1 kg ballast washload. For each wash two tablets (Examples 4 to 6) or 80 g of powder
(Comparative Examples A to C) were used. The results are shown in Table 3.

Example 7, Comparative Example D
(i) Preparation of bleach compositions
[0087] A spray-dried sodium carbonate composition was prepared as described for Examples
4 to 6. Bleach compositions were then prepared by dry-mixing the spray-dried sodium
carbonate composition with sodium percarbonate, 1-O-octanoyl-2,3,4,6-tetra-O-acetyl
glucose (OTAG) and glycerol as shown in Table 4.

(ii) Tabletting
[0088] Tablets were prepared using an Instron (Trade Mark) Model 4202 Materials Testing
Machine fitted with a 5KN load cell.
[0089] The tablets each weighed 25.62 g and were 40 mm in diameter and 13 mm in thickness.
[0090] Comparative Example D was a loose powder of the same composition.
(iii) Bleaching performance
[0091] Bleaching performance was assessed by measuring the increase in reflectance at 460
nm (with incident light <400 nm filtered out) (δR
460*) of standard tea-stained test cloths after washing in a Miele (Trade Mark) 756 front-loading
washing machine, in 10 litres of soft water in the presence of a buffer containing
10g/l sodium metaborate and 5g/l sodium bicarbonate at pH 9.85 at 20°C for 30 minutes.
For each wash one tablet (Example 7) or 25.8g of powder (Comparative Example D) were
used. The results are shown in Table 5.

Example 8, Comparative Examples E and F
(i) Preparation of bleach compositions
[0092] A spray-dried sodium carbonate composition was prepared as described for Examples
4 to 6. Bleach compositins were then prepared by dry-mixing the spray-dried sodium
carbonate composition with sodium percarbonate and OTAG as shown in Table 6.

(ii) Tabletting
[0093] Tablets were prepared as described for Example 7.
[0094] Comparative Examples E and F were loose powders of the same composition.
(iii) Preparation of detergent base powder composition
[0095] A detergent base composition was prepared to the formulation shown in Table 7, by
spray-drying an aqueous slurry of all ingredients except the nonionic surfactant 7EO
which was subsequently sprayed on.

(iv) Bleaching performance
[0096] Bleaching performance was assessed by measuring the increase in reflectance at 460
nm (with incident light >400 nm filtered out) (δR₄₆₀) of both standard tea-stained
test cloths and EMPA wine stained cloths after washing in a Miele (Trade Mark) 756
front-loading machine, in 10 litres of water at 40°C. For each wash one tablet (Example
8) or 25.8g of bleach composition powder (Comparative Examples E and F) were used
in conjunction with 50g of the described detergent base powder. For Comparative Example
E the bleach composition powder was added to 20 ml of water in a bottle and shaken
vigorously for one minute for adding to the wash, thus enabling some perhydrolysis
to take place under conditions of high concentration and pH prior to the bleach performance
test described above. The results are shown in Table 8.

Examples 9 to 13, Comparative Example G
[0097] The effect of tabletting pressure on peracid yield using the bleach composition of
Example 3 (containing TAED as bleach activator) was investigated. The results are
shown in Table 9.
[0098] For this work, separate bleach and detergent tablets were prepared, so that the bleach
composition could be tabletted at a series of different pressures (0.4 to 8 KN/cm²)
while the detergent base powder was always tabletted at the same pressure (0.4 KN/cm²),
thus avoiding complications that would have arisen if the detergent base powder had
dissolved at different rates in the different experiments.
[0099] In each experiment, two bleach composition tablets (each 10 g) and two detergent
base composition tablets (each 30 g) were used.
[0100] Wash conditions, selected to obtain maximum reproducibility, were a long (45 minute)
wash at ambient temperature in the Miele 756 washing machine in the absence of a ballast
load.
[0101] Peracid yields, expressed as a percentage of the theoretical yield, were measured
by a standard iodine/thiosulphate titration at 0°C at intervals throughout the wash:
the maximum yield, and the time (T
max) taken to reach that maximum, were recorded.
[0102] The integrated yield (arbitrary units) was also calculated, by numerical integration
of the peracid yield over the whole wash time: this is a measure of the peracid level
available over the whole of the wash period.

[0103] It may be seen that at the optimum (a tabletting pressure of 4.8 KN/cm) the integrated
yield was just over 115% of that for the powdered formulation.
Examples 14 to 18, Comparative Example H
[0104] The procedure of Examples 9 to 13 and G was repeated using a bleach formulation containing
sodium perborate tetrahydrate and TAED.
[0105] The formulation was adjusted slightly in order to maintain the same levels of available
oxygen as in Examples 9 to 13 and G, since commercial sodium perborate tetrahydrate
contains about 10% available oxygen while sodium percarbonate contains about 13.5%.
This adjustment increased the weight of the bleach tablets from 10 g to 11.75 g, while
the weight of the detergent tablets remained at 30 g. The bleach formulation was as
follows:

[0106] Again, two bleach tablets and two detergent tablets were used per wash.
[0107] The results are shown in Table 10. Some benefit was observed at higher tabletting
pressures, but it was smaller than the benefit observed with sodium percarbonate.
