TECHNICAL FIELD OF INVENTION
[0001] The present invention relates to novel laundry detergent compositions in the form
of tablets containing inorganic persalt bleach (sodium perborate) and bleach-sensitive
ingredients together without segregation.
BACKGROUND AND PRIOR ART
[0002] Modern high-performance detergent powders for use in automatic washing machines normally
contain inorganic persalt bleach as well as certain ingredients, notably bleach activators,
enzymes and optical brighteners, that are sensitive to bleach.
[0003] Detergent compositions in tablet form are known in the art, as discussed below, and
some products are now on the market. Tablets have several advantages over powdered
products: they do not require measuring and are thus easier to handle and dispense
into the washload, they are non-dusting and thus their components are less irritating
to sensitive skin, and they are more compact, hence facilitating more economical storage.
[0004] However, the ingredients are much more intimately associated with one another in
a compressed tablet environment than in a powder, and any adverse interactions and
instability will be exacerbated. Hitherto it has not been considered possible to prepare
a satisfactory tablet containing both bleach and bleach-sensitive ingredients without
some kind of segregation or separation.
[0005] Detergent tablets containing persalt bleach without bleach sensitive ingredients
are described, for example, in US 3 953 350 (Kao), JP 60 015 500A (Lion), JP 60 135
497A (Lion) and JP 60 135 498A (Lion). Detergent tablets containing enzyme but no
bleach are sold commercially in Spain. GB 911 204 (Unilever) discloses layered detergent
tablets containing sodium perborate and certain bleach activators, for example, sodium
acetoxybenzene sulphonate and phthalic anhydride, and shows by means of comparative
examples that tablets containing those ingredients together, without segregation into
separate layers, are unstable.
[0006] Surprisingly, it has now been found that if the bleach activator is a N-diacylated
or N,N'-polyacylated amine, notably tetraacetylethylenediamine (TAED), such segregation
is unnecessary. Similarly, other bleach-sensitive ingredients, notably enzymes and
fluorescers, can also be included without the need for segregation, thus greatly simplifying
tablet manufacture. Fully-formulated detergent tablets in accordance with the invention
may be made simply by compressing a powder.
DEFINITION OF THE INVENTION
[0007] The present invention accordingly provides a tablet of compressed detergent powder
comprising:
(a) sodium perborate;
(b) one or more ingredients sensitive to inorganic persalt bleach selected from
(b1) N-diacylated and N,N'-polyacylated amine bleach activators,
(b2) enzymes, and
(b3) fluorescers;
(c) one or more detergent-active compounds, one or more detergency builders, and optionally
other detergent ingredients;
wherein ingredients (a) and (b) are not segregated from one another.
[0008] The invention also provides a process for the preparation of a detergent tablet,
which comprises the following steps:
(i) preparing a detergent powder comprising:
(a) sodium perborate;
(b) one or more ingredients sensitive to inorganic persalt bleach selected from
(b1) N-diacylated and N,N'-polyacylated amine bleach activators,
(b2) enzymes, and
(b3) fluorescers;
(c) one or more detergent-active compounds, one or more detergency builders, and optionally
other detergent ingredients;
(ii) compressing the powder to form a tablet in which ingredients (a) and (b) are
not segregated from one another.
DESCRIPTION OF THE INVENTION
[0009] The detergent tablet of the invention contains as essential ingredients inorganic
persalt bleach (sodium perborate), and at least one bleach-sensitive ingredient -
acylated amine bleach activator, enzyme, fluorescer - as well as surfactant, detergency
builder and optionally other conventional ingredients. The various ingredients are
described in more detail below.
[0010] It is an essential feature of the invention that the sodium perborate (a) and the
bleach-sensitive ingredient or ingredients (b) are not segregated from one another
in the tablet. This means in effect that those ingredients are randomly mixed with
one another rather than isolated from one another in specific areas of the tablet,
for example, in separate layers or inserts. It does not, however, preclude the presentation
of those ingredients in any of the forms commonly used in detergent powders, for example,
bleach activators as granules, enzymes as granules or marumes or coated marumes, even
though these forms may involve some measure of protection, coating or dilution. However,
in the tablet of the present invention, no additional measures are taken, over and
above those normal in detergent powders, to keep the sodium perborate (a) and the
bleach-sensitive ingredient or ingredients (b) apart.
[0011] According to one preferred embodiment of the invention, the tablet of the invention
is substantially homogeneous, that is to say, it is preparable by compression of a
single, homogeneously mixed powder.
[0012] It is also within the scope of the invention, however, for the tablet to include
one or more separate layers, inserts or other measures in order to segregate ingredients
other than (a) and (b). In that case, the ingredients (a) and (b) are randomly mixed
and distributed in at least one region of the tablet.
The sodium perborate (a)
[0013] The inorganic persalt bleach employed in the detergent tablet of the invention is
sodium perborate. This may be in the form of the monohydrate, the tetrahydrate, a
mixture of the two, a partially dehydrated tetrahydrate, or any other stable commercially
available form. Sodium perborate monohydrate may be either in high-surface-area or
low-surface-area form. The sodium perborate is preferably present in an amount within
the range of from 1 to 30 wt%, more preferably from 5 to 20 wt%.
The bleach-sensitive ingredient (b)
[0014] The tablet of the invention contains as an essential ingredient at least one bleach
sensitive ingredient selected from one cf the classes (b1), (b2) and (b3). Any combination
of more than one bleach-sensitive ingredients from any one or more of these classes
may be present.
The bleach activator (b1)
[0015] An activator for an inorganic persalt is an organic compound having one or more reactive
acyl residues which cause the formation of peracids, the latter providing a more effective
bleaching action at a low wash temperature, eg from 20 to 60°C, than is possible using
the inorganic persalt alone.
[0016] The bleach activator used in the tablet of the present invention is an N-diacylated
or N,N'-polyacylated amine. These materials are disclosed in GB 855 355 and GB 907
356 (Unilever). In polyamines, at least one nitrogen atom must carry two acyl groups.
The preferred bleach activator for use in the tablets of the present invention is
tetraacetylethylenediamine (TAED).
[0017] The ratio by weight of the inorganic persalt (sodium perborate) to the bleach activator
in the tablet of the invention may vary from about 30:1 to about 1:1, and is preferably
from 15:1 to 2:1.
[0018] TAED is conveniently employed in granular form, on an inorganic carrier. The amount
of TAED itself in the tablet of the invention is preferably from 1 to 15 wt%, more
preferably from 2 to 10 wt%.
The enzyme (b2)
[0019] Various detergency enzymes well-known in the art for their ability to degrade and
aid in the removal of various soils and stains may optionally be employed in the detergent
tablets of the invention.
[0020] 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. The present invention is particularly concerned with proteolytic enzymes
(proteases).
[0021] Preferred proteases are normally solid, catalytically active protein materials which
degrade or alter protein types of stains when present as in fabric stains in a hydrolysis
reaction. They may be of any suitable origin, such as vegetable, animal, bacterial
or yeast origin.
[0022] Proteases of various qualities and origins and having activity in various pH ranges
of from 4-12 are available and can be used in the detergent tablet of the invention.
Examples of suitable proteases are the subtilisins, which are obtained from particular
strains of
B.
subtilis and
B.
licheniformis, such as the commercially available subtilisins Maxatase (Trade Mark), as supplied
by Gist-Brocades N.V., Delft, Holland, and Alcalase (Trade Mark), as supplied by Novo
Industri A/S, Copenhagen, Denmark.
[0023] Particularly suitable for use in the present invention is a protease obtained from
a strain of Bacillus having maximum activity throughout the pH range of 8-12, being
commercially available, e.g. from Novo Industri A/S under the registered trade-names
Esperase (Trade Mark) and Savinase (Trade-Mark). The preparation of these and analogous
enzymes is described in GB 1 243 785. Other commercial proteases are Kazusase (Trade
Mark) (obtainable from Showa-Denko of Japan), Optimase (Trade Mark) (from Miles Kali-Chemie,
Hannover, West Germany), and Superase (Trade Mark) (obtainable from Pfizer of U.S.A.).
[0024] 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.
The fluorescer (b3)
[0025] Any fluorescer (optical brightener) suitable for use in a detergent powder may be
used in the detergent tablet of the present invention.
[0026] The most commonly used fluorescers are those belonging to the classes of diaminostilbene-sulphonic
acid derivatives, diarylpyrazoline derivatives and bisphenyl-distyryl derivatives.
[0027] Examples of the diaminostilbene-sulphonic acid derivative type of fluorescer include
disodium 4,4'-bis-(2- diethanolamino-4-anilino-s-triazin-6-ylamino) stilbene- 2:2'-disulphonate,
disodium 4,4'-bis-(2-morpholino-4-anilino-s-triazin-6-ylamino-stilbene-2:2'-disulphonate,
disodium 4,4'-bis-(2,4-dianilino-s-triazin-6-ylamino) stilbene-2:2'-disulphonate,
disodium 4,4'-bis-(2-anilino-4-(N-methyl-N-2-hydroxyethylamino)-s-triazin-6-ylamino)
stilbene-2,2'-disulphonate, disodium 4,4'-bis-(4-phenyl-2,1,3-triazol-2-yl) stilbene-2,2'-disulphonate,
disodium 4,4'-bis(2-anilino-4-(1-methyl-2-hydroxyethylamino)-s-triazin-6-ylamino)stilbene-2,2'-disulphonate
and sodium 2-(stilbyl-4''-naptho-1',2':4,5)-1,2,3-triazole-2''-sulphonate.
[0028] Preferred fluorescers are Tinopal (Trade Mark) DMS and 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.
[0029] Other fluorescers suitable for use in the invention include the 1,3-diaryl pyrazolines
and the 7-alkylaminocoumarins.
[0030] Fluorescer is preferably present in an amount within the range of from 0.02 to 0.8
wt%, more preferably from 0.03 to 0.5 wt%.
The surfactant system
[0031] The total amount of detergent-active material (surfactant) in the detergent tablet
of the invention is suitably from 2 to 50% by weight, and is preferably from 5 to
40% by weight.
[0032] The detergent tablet of the invention may contain one or more soap or non-soap anionic,
nonionic, cationic, amphoteric or zwitterionic surfactants, or combinations of these.
Many suitable detergent-active compounds are available and are fully described in
the literature, for example, in "Surface-Active Agents and Detergents", Volumes I
and II, by Schwartz, Perry and Berch.
[0033] The preferred detergent-active compounds that can be used are soaps and synthetic
non-soap anionic surfactants and nonionic surfactants.
[0034] 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 C
8-C
15; primary and secondary alkyl sulphates, particularly sodium C
12-C
15 primary alcohol sulphates; olefin sulphonates; alkane sulphonates; dialkyl sulphosuccinates;
and fatty acid ester sulphonates.
[0035] 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.
[0036] Specific nonionic detergent compounds are alkyl (C
6-22) phenol-ethylene oxide condensates, the condensation products of linear or branched
aliphatic C
8-20 primary or secondary alcohols wih ethylene oxide, and products made by condensation
of ethylene oxide with the reaction products of propylene oxide and ehylenediamine.
Other so-called nonionic detergent compounds include long-chain tertiary amine oxides,
tertiary phosphine oxides, and dialkyl sulphoxides.
[0037] Especially preferred are the primary and secondary alcohol ethoxylates, especially
the C
12-15 primary and secondary alcohols ethoxylated with an average of from 5 to 20 moles
of ethylene oxide per mole of alcohol.
[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 rape seed oil.
[0039] Detergent compositions suitable for use in automatic fabric washing machines generally
contain anionic surfactant, or nonionic surfactant, or a combination of the two in
any proportions. Soap may also be present if desired, in any amount from 0 to 40%
by weight of the composition. Generally, compositions of this type may successfully
be presented in the form of tablets in accordance with the present invention.
The builder system
[0040] The detergent tablets of the invention contain one or more detergency builders, suitably
in an amount of from 5 to 80 wt%, preferably from 20 to 80 wt%.
[0041] Especially preferred are alkali metal phosphates, alkali metal aluminosilicates,
and combinations thereof.
[0042] Preferred alkali metal phosphates are sodium orthophosphate, sodium pyrophosphate
and sodium tripolyphosphate. Sodium tripolyphosphate is especially preferred. It may
generally be present in amounts up to 50% by weight of the composition.
[0043] Alkali metal (preferably sodium) aluminosilicates may generally be incorporated in
amounts up to 60% by weight of the composition, and may be either crystalline or amorphous
or mixtures thereof, having the general formula:
0.8-1.5 Na
20. Al
20
3.0.8-6 Si0
2
[0044] 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
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.
[0045] Suitable crystalline sodium aluminosilicate ion-exchange detergency builders are
described, for example, in GB 1 429 143 (Proctor & Gamble). The preferred sodium aluminosilicates
of this type are the well-known commercially available zeolites A and X, and mixtures
thereof. Especially preferred is zeolite 4A.
[0046] 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 nitrilotriacetates, citrates and carboxymethyloxysuccinates.
[0047] Especially preferred supplementary builders are polycarboxylate polymers, especially
those containing (meth)acrylate and/or maleate units. These polymers also provide
certain additional benefits, for example, reduced soil redisposition. The polymers
are suitably used in amounts of from 0.5 to 10% wt%, more preferably from 1 to 6 wt%.
The polymers may be in acid form or in wholly or partially neutralised salt form.
Preferred polymers are homopolymers and copolymers of acrylic acid. Of especial interest
are polyacrylates, acrylic/maleic acid copolymers, and acrylic phosphinates: acrylic/maleic
copolymers, for example, Sokalan (Trade Mark) CP5 ex BASF are especially preferred.
Other ingredients
[0048] Further ingredients which can optionally be employed in the detergent tablet of the
invention include anti-redeposition agents such as sodium carboxymethylcellulose,
polyvinyl pyrrolidone and the cellulose ethers such as methyl cellulose and ethyl
hydroxyethyl cellulose; stabilisers such as ethylenediamine tetramethylene phosphonate
and diethylenetriamine pentamethylene phosphonate; fabric-softening agents; lather
control agents or lather boosters as appropriate; heavy metal sequestrants such as
EDTA; perfumes; colourants; 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.
[0049] An antifoam material is advantageously included in the detergent 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.
[0050] It may also be desirable to include in the 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.
Preparation of the detergent tablet
[0051] The detergent compositions of the invention are made into tablet form by compression
of a powder. As previously mentioned, according to one preferred embodiment of the
invention the tablets of the invention are substantially homogeneous, that is to say,
they are formed by compression of a single, substantially homogeneous powder without
the addition of inserts, separate layers containing segregated ingredients, coatings,
etc.; this greatly facilitates manufacture. However, it is also within the scope of
the invention, for example, for the starting powder to contain inserts or other local
regions of segregation that will persist into the tablet; or for two or more different
powders to be compressed to form separate layers in the final tablet; the only proviso
being that the ingredients (a) and (b) should not be segregated.
[0052] The powder itself may be made by any suitable method, for example, mixing, granulation,
or any combination of these, optionally with spray-on of liquid ingredients. For example,
solid ingredients may be dry-mixed, water and/or liquid ingredients added, the mixture
granulated, and then dried. Another method involves spray-drying an aqueous slurry
of detergent components to form granules, and subsequently post-dosing heat-sensitive
ingredients, such as bleach and enzymes; again liquid ingredients may be sprayed on
at any suitable stage in the process.
[0053] One preferred process involving spray-drying comprises the steps of:
(i) spray-drying an aqueous slurry to form a base powder including one or more detergent-active
compounds and one or more detergency builders, any fluorescer (b3) to be included,
and other ingredients as desired;
(ii) admixing to the base powder the sodium perborate (a), any N-diacylated or N,N'-polyacylated
amine bleach activator (b1) and/or enzyme (b2) to be included, and optionally other
ingredients as desired, to form a homogeneous powder;
(iii) compressing the powder to form a tablet.
Dosage forms
[0054] The detergent tablet of the invention may be, and preferably is, 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.
[0055] Although one tablet may contain sufficient of all the components to provide the correct
amount required for an average washload, it is preferred that each tablet should contain
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 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.
EXAMPLES
[0056] The invention will now be illustrated by the following non-limiting Examples in which
parts are percentages are by weight. Examples and compositions identified by numbers
are within the invention, while those identified by letters are comparative.
Example 1
[0057] A zero-phosphate detergent base powder containing fluorescer was prepared to the
following composition by spray-drying, followed by spray-on of the 3EO nonionic surfactant:
|
% |
Linear alkylbenzene sulphonate |
9.2 |
C12-C15 7EO nonionic surfactant |
4.2 |
C13-C15 3EO nonionic surfactant |
9.2 |
Fatty acid soap |
2.5 |
Zeolite 4A (anhydrous basis) |
36.8 |
Acrylic/maleic copolymer (Sokalan* CP5) |
6.0 |
Sodium silicate |
0.7 |
Sodium carboxymethyl cellulose |
0.8 |
Fluorescers (Tinopal** DMS and Tinopal** CBS-X) |
0.3 |
Sodium carbonate |
12.9 |
Water |
to 100.0 |
*Trade Mark; ex BASF AG, Ludwigshafen, Germany. |
**Trade Mark; ex Ciba-Geigy AG, Basel, Switzerland. |
[0058] Tablets and powders were prepared to the compositions given below. The enzyme was
the granular protease Savinase (Trade Mark) 6.0T, the sodium perborate was high-surface-area
(5.9 m
2/g) monohydrate, and the TAED was in granular form (83 wt% TAED, 17 wt% inert zero-phosphate
carrier).
Example |
1 Tablet |
P Powder |
Base |
85.4 |
85.4 |
Enzyme |
1.0 |
1.0 |
Perborate |
10.0 |
10.0 |
TAED granules |
3.6 |
3.6 |
[0059] Tablets were made by compressing the powders at 1.5 kN by means of an Instron (Trade
Mark) constant speed extensiometer, using a crosshead speed of 100 mm/min. Each tablet
weighed 60 g and had a diameter of 53 mm and a thickness of about 25 mm.
[0060] The bleach, fluorescer and enzyme performances of the tablets and powders were compared
for the freshly made compositions, and after 1 week's and 2 weeks' storage under severe
conditions (37°C and 70% relative humidity, unprotected, no carton). The comparisons
were carried out by washing selected testcloths in the tergotometer using a 40°C isothermal
wash for 15 minutes in 1 litre of 12° (French) hard water. The tablets were crushed
prior to the wash, and dosed at 5 g/litre; the powders were also dosed at 5 g/litre.
[0061] Table 1 shows the enzyme results, obtained using an enzyme-sensitive testcloth (casein
soil on polyester/cotton fabric), expressed as reflectance differences (delta R at
460 nm).
Table 1
Example |
Time (weeks) |
|
0 |
1 |
2 |
1 (tablet) |
26.9 |
26.8 |
26.9 |
P (powder) |
27.0 |
26.6 |
26.4 |
[0062] There was no evidence of increased enzyme decomposition in the tablet as compared
with the powder, despite the close proximity to the bleach ingredients.
[0063] Table 2 shows the fluorescer results, obtained using a fluorescer-sensitive testcloth,
and expressed as the difference between the reflectances (delta R 460) in the presence
and in the absence of ultraviolet light.
Table 2
Example |
Time (weeks) |
|
0 |
1 |
2 |
1 (tablet) |
15.7 |
16.6 |
15.7 |
P (powder) |
15.6 |
16.2 |
15.3 |
[0064] Again, no significant differences between tablet and powder were found.
[0065] Table 3 shows the bleach results, obtained using a tea-stained cotton testcloth and
expressed as reflectance differences (delta R at 460 nm).
Table 3
Example |
Time (weeks) |
|
0 |
1 |
2 |
1 (tablet) |
5.3 |
4.3 |
4.0 |
P (powder) |
3.8 |
3.1 |
3.2 |
[0066] Surprisingly, the results were consistently better for the tablet than for the powder
of identical composition.
Example 2
[0067] A phosphate-built base detergent base powder containing fluorescer was prepared to
the following composition by spray-drying, followed by spray-on of the 3EO nonionic
surfactant:
|
% |
Linear alkylbenzene sulphonate |
8.3 |
C12-C15 7EO nonionic surfactant |
5.3 |
C13-C15 3EO nonionic surfactant |
3.5 |
Fatty acid soap |
0.7 |
Sodium tripolyphosphate |
29.3 |
Acrylic/maleic copolymer (Sokalan CP5) |
1.2 |
Sodium silicate |
7.0 |
Sodium carboxymethyl cellulose |
0.4 |
EDTA |
0.15 |
Fluorescers (Tinopal DMS and Tinopal CBS-X) |
0.35 |
Sodium carbonate |
5.9 |
Sodium sulphate, water |
to 100.0 |
[0068] Tablets and powders were prepared as described in Example 1 to the compositions given
below. The enzyme, sodium perborate monohydrate and TAED were as in Example 1.
Example |
2 Tablet |
Q Powder |
Base |
85.4 |
85.4 |
Enzyme |
1.0 |
1.0 |
Perborate |
10.0 |
10.0 |
TAED granules |
3.6 |
3.6 |
[0069] The bleach, fluorescer and enzyme performances of the tablets and powders were compared
as described in Example 1. Enzyme results are shown in Table 4, fluorescer results
in Table 5, and bleach results in Table 6.
Table 4
(enzyme) |
Example |
Time (weeks) |
|
0 |
1 |
2 |
2 (tablet) |
26.6 |
27.1 |
25.8 |
Q (powder) |
26.8 |
26.1 |
25.7 |
Table 5
(fluorescer) |
Example |
Time (weeks) |
|
0 |
1 |
2 |
2 (tablet) |
16.1 |
15.4 |
15.6 |
Q (powder) |
15.0 |
15.5 |
15.3 |
[0070] Again, no significant differences between tablet and powder were found.
Table 6
(bleach) |
Example |
Time (weeks) |
|
0 |
1 |
2 |
2 (tablet) |
6.0 |
5.4 |
5.0 |
Q (powder) |
5.6 |
5.2 |
4.3 |
[0071] Bleach loss on storage was observed, as expected, but surprisingly the results were
consistently better for the tablet than for the powder.
Examples 3 to 5
[0072] A further series of comparisons was carried out using the zero-phosphate base powder
of Example 1, and three different types of sodium perborate:
high-surface-area (5.9 m
2/g) monohydrate,
low-surface-area (3.2 m
2/g) monohydrate, and
tetrahydrate.
[0073] Tablets and powders were prepared to the following compositions, Examples 3, 4 and
5 being tablets and Examples R, S and T being powders:
Example |
3, R |
4, S |
5, T |
Base |
89.0 |
89.0 |
84.0 |
Enzyme |
1.0 |
1.0 |
1.0 |
Perborate : |
|
|
|
Mono (HSA) |
10.0 |
- |
- |
Mono (LSA) |
- |
10.0 |
- |
Tetra |
- |
- |
15.0 |
[0074] Bleach and enzyme performances of the fresh compositions, and after storage for 2
and 4 weeks (37°C, 70% relative humidity), were compared by the methods described
in Example 1. The results are shown below in Tables 7 (bleach) and 8 (enzyme).
Table 7
(bleach) |
Example |
Time (weeks) |
|
0 |
4 |
3 (tablet) |
2.3 |
0.9 |
R (powder) |
1.5 |
1.1 |
4 (tablet) |
2.0 |
0.8 |
S (powder) |
2.4 |
0.5 |
5 (tablet) |
1.3 |
1.6 |
T (powder) |
2.3 |
0.8 |
[0075] When perborate monohydrate was present, bleach performance always deteriorated after
4 weeks' storage, as expected, but that was no worse in the tablets than in the powders,
and, surprisingly, there was less loss of performance from the tablet than from the
powder in the case of the low-surface-area material. When the perborate was in tetrahydrate
form, an even better result for the tablet was obtained.
Table 8
(enzyme) |
Example |
Time (weeks) |
|
0 |
2 |
4 |
3 (tablet) |
29.1 |
31.8 |
34.1 |
R (powder) |
33.6 |
34.5 |
32.8 |
4 (tablet) |
33.4 |
32.3 |
33.2 |
S (powder) |
34.3 |
34.1 |
34.2 |
5 (tablet) |
33.0 |
32.2 |
33.8 |
T (powder) |
33.4 |
33.1 |
32.9 |
[0076] No significant differences were observed.
Examples 6 to 8
[0077] The exercise of Examples 3 to 5 was repeated using a similar series of compositions
additionally containing TAED (83 wt% zero-phosphate granules as used in Example 1).
Tablets and powders were prepared to the following compositions, Examples 6, 7 and
8 being tablets and Examples U, V and W being powders:
Example |
6, U |
7, V |
8, W |
Base |
85.4 |
85.4 |
80.4 |
Enzyme |
1.0 |
1.0 |
1.0 |
Perborate : |
|
|
|
Mono (HSA) |
10.0 |
- |
- |
Mono (LSA) |
|
10.0 |
- |
Tetra |
|
- |
15.0 |
TAED granules |
3.6 |
3.6 |
3.6 |
[0078] Bleach and enzyme performances of the fresh compositions, and after storage for 2
and 4 weeks (37°C, 70% relative humidity), were compared as described in Example 1,
the results being shown below in Tables 9 (bleach) and 10 (enzyme).
Table 9
(bleach) |
Example |
Time (weeks) |
|
0 |
4 |
6 (tablet) |
2.7 |
3.3 |
U (powder) |
4.4 |
3.0 |
7 (tablet) |
3.8 |
3.2 |
V (powder) |
4.0 |
3.5 |
8 (tablet) |
4.0 |
3.3 |
W (powder) |
4.1 |
3.6 |
[0079] No significant differences between tablets and powders were observed.
Table 10
(enzyme) |
Example |
Time (weeks) |
|
0 |
2 |
4 |
6 (tablet) |
33.4 |
31.7 |
34.1 |
U (powder) |
32.6 |
33.8 |
32.4 |
7 (tablet) |
33.5 |
32.5 |
33.8 |
V (powder) |
32.2 |
32.7 |
33.5 |
8 (tablet) |
33.3 |
33.6 |
33.6 |
W (powder) |
33.3 |
33.9 |
32.6 |
[0080] No significant differences were observed.
Examples 9 and 10
[0081] Examples 3 and 6 were repeated using the phosphate-built base powder of Example 2
instead of the zero-phosphate base powder of Example 1. Tablets and powders were prepared
to the following compositions, Examples 9 and 10 being tablets and Examples X and
Y being powders:
Example |
9, X |
10, Y |
Base |
89.0 |
85.4 |
Enzyme |
1.0 |
1.0 |
Perborate (mono, HSA) |
10.0 |
10.0 |
TAED granules |
- |
3.6 |
[0082] Bleach and enzyme performances of the fresh compositions, and after storage for 2
and 4 weeks (37°C, 70% relative humidity), were compared as described in Example 1,
the results being shown below in Tables 11 (bleach) and 12 (enzyme).
Table 11
(bleach) |
Example |
Time (weeks) |
|
0 |
4 |
9 (tablet) |
1.7 |
1.9 |
X (powder) |
2.4 |
1.1 |
10 (tablet) |
5.7 |
4.4 |
Y (tablet) |
5.0 |
4.1 |
[0083] The tablet showed better bleach performance than the corresponding powder after 4
weeks' storage.
Table 12
(enzyme) |
Example |
Time (weeks) |
|
0 |
2 |
4 |
9 (tablet) |
34.1 |
32.4 |
32.0 |
X (powder) |
32.6 |
33.5 |
31.4 |
10 (tablet) |
34.3 |
32.4 |
31.4 |
Y (powder) |
32.1 |
31.3 |
32.8 |
[0084] No significant differences were observed.
Example 11
[0085] A phosphate-built detergent powder containing sodium perborate tetrahydrate bleach
in conjunction with proteolytic enzyme (Savinase) and fluorescers was prepared, by
spray-drying and postdosing, to the following composition:
|
% |
Linear alkylbenzene sulphonate |
18.0 |
C12-C15 7EO nonionic surfactant |
8.0 |
Fatty acid soap |
2.0 |
Sodium tripolyphosphate |
30.0 |
Acrylic/maleic copolymer (Sokalan CP5) |
1.5 |
Alkaline sodium silicate |
10.0 |
Sodium carboxymethyl cellulose |
0.5 |
EDTA |
0.25 |
Fluorescers: |
Tinopal DMS |
0.13 |
Tinopal CBS-X |
0.08 |
Sodium sulphate |
3.6 |
Sodium perborate tetrahydrate |
10.0 |
Enzyme (Savinase 6CM) |
0.75 |
Antifoam granules |
3.0 |
Perfume |
0.22 |
Moisture, salts |
to 100.0 |
[0086] The powder had a bulk density of 400-425 g/litre. It was compressed to approximately
half its volume, using a pilot-scale tabletting machine, to form tablets weighing
32 g and having a diameter of 50 mm and a height of 23 mm.
[0087] The tablets displayed effective washing and cleaning performance in the washing machine,
two tablets being an appropriate dosage for soft water and three for hard water.
Example 12
[0088] A phosphate-built detergent powder containing sodium perborate tetrahydrate bleach
in conjunction with TAED granules, proteolytic enzyme (Savinase) and fluorescers was
prepared, by spray-drying and postdosing, to the following composition, and then compressed
as described in Example 11 to form tablets:
|
% |
Linear alkylbenzene sulphonate |
18.0 |
C12-C15 7EO nonionic surfactant |
8.0 |
Fatty acid soap |
2.0 |
Sodium tripolyphosphate |
30.0 |
Acrylic/maleic copolymer (Sokalan CP5) |
1.5 |
Alkaline sodium silicate |
10.0 |
Sodium carboxymethyl cellulose |
0.5 |
EDTA |
0.25 |
Fluorescers: |
Tinopal DMS |
0.13 |
Tinopal CBS-X |
0.08 |
Sodium sulphate |
1.3 |
Sodium perborate tetrahydrate |
10.0 |
TAED granules (83 wt% active) |
2.4 |
Enzyme (Savinase 6CM) |
0.75 |
Antifoam granules |
3.0 |
Perfume |
0.22 |
Moisture, salts |
to 100.0 |
[0089] The tablets displayed effective cleaning and washing performance when used at a dosage
of two to three tablets per wash.
Example 13
[0090] A phosphate-built detergent powder with enhanced bleaching performance, containing
sodium perborate monohydrate bleach in conjunction with TAED, proteolytic enzyme (Savinase)
and fluorescers, was prepared to the following composition by spray-drying and postdosing:
|
% |
Linear alkylbenzene sulphonate |
18.0 |
C12-C15 7EO nonionic surfactant |
8.0 |
Fatty acid soap |
2.0 |
Sodium tripolyphosphate |
30.0 |
Acrylic/maleic copolymer (Sokalan* CP5) |
1.5 |
Alkaline sodium silicate |
10.0 |
Sodium carboxymethyl cellulose |
0.5 |
EDTA |
0.25 |
Fluorescers: |
Tinopal DMS |
0.13 |
Tinopal CBS-X |
0.08 |
Salts |
4.24 |
Water |
8.0 |
Sodium perborate monohydrate |
10.0 |
TAED |
3.33 |
Enzyme (Savinase 6CM) |
0.75 |
Antifoam granules |
3.0 |
Perfume |
0.22 |
*Trade Mark; ex BASF AG, Ludwigshafen, Germany. |
[0091] The powder was compressed as described in Example 11 to form tablets, each weighing
26-28 g, having a diameter of 40 mm and a thickness of 26 mm. The tablets displayed
effective washing and cleaning performance when used at a dosage of two or three tablets
per wash.
Examples 14 and 15
[0092] The following zero-phosphate detergent powders, containing sodium perborate monohydrate
bleach in conjunction with TAED, proteolytic enzyme (Savinase) and fluorescers, prepared
by spray-drying and postdosing, are suitable for compression to form 40 g tablets
according to the present invention.
|
14 |
15 |
Linear alkylbenzene sulphonate |
16.0 |
6.0 |
C12-C15 7EO nonionic surfactant |
3.0 |
4.5 |
C13-C15 3EO nonionic surfactant |
5.0 |
4.0 |
Fatty acid soap |
2.0 |
- |
Zeolite 4A (anhydrous basis) |
30.0 |
37.0 |
Acrylic/maleic copolymer (Sokalan CP5) |
4.0 |
5.0 |
Sodium carboxymethyl cellulose |
0.5 |
0.5 |
Fluorescers: |
Tinopal DMS-X |
0.13 |
0.13 |
Tinopal CBS-X |
0.08 |
0.07 |
Sodium carbonate |
9.0 |
14.9 |
Sodium perborate monohydrate |
10.0 |
7.5 |
TAED granules (83%) |
4.5 |
4.5 |
Enzyme (Savinase 6.0T) |
1.0 |
1.0 |
Antifoam granules |
3.0 |
1.5 |
Perfume |
0.4 |
0.4 |
Water and minor ingredients to 100.0 |
1. A tablet of compressed detergent powder characterised in that it comprises:
(a) sodium perborate
(b) one or more ingredients sensitive to inorganic persalt bleach selected from
(b1) N-diacylated and N,N'-polyacylated amine bleach activators,
(b2) enzymes, and
(b3) fluorescers;
(c) one or more detergent-active compounds, one or more detergency builders, and optionally
other detergent ingredients;
wherein ingredients (a) and (b) are not segregated from one another.
2. A detergent tablet in claim 1, wherein the sodium perborate (a) is present as sodium
perborate monohydrate, and containing up to 60% by weight of alkali metal aluminosilicate
detergency builder.
3. A detergent tablet as claimed in either claim 1 or claim 2, characterised in that
the sodium perborate (a) is present in an amount within the range of from 1 to 30
wt%.
4. A detergent tablet as claimed in any preceding claim, comprising a bleach activator
(b1), characterised in that the weight ratio of sodium perborate (a) to bleach activator
(b1) is within the range of from 30:1 to 1:1.
5. A detergent tablet as claimed in either claim 1 or claim 2, characterised in that
it comprises as bleach activator tetraacetylethylenediamine.
6. A detergent tablet as claimed in claim 5, characterised in that the tetraacetylethylenediamine
is in granular form and is present in an amount within the range of from 1 to 15 wt%.
7. A detergent tablet as claimed in claim 6, characterised in that the tetraacetylethylenediamine
is in granular form and is present in an amount within the range of from 2 to 10 wt%.
8. A detergent tablet as claimed in any preceding claim, characterised in that it comprises
an enzyme (b2) in granular form in an amount within the range of from 0.1 to 3.0 wt%.
9. A detergent tablet as claimed in claim 8, characterised in that the enzyme is a protease.
10. A detergent tablet as claimed in any preceding claim, characterised in that it is
substantially homogenous.
11. A process for the preparation of a detergent tablet, characterised by the steps of:
(i) preparing a detergent powder comprising:
(a) sodium perborate
(b) one or more ingredients sensitive to inorganic persalt bleach selected from
(b1) N-diacylated and N,N'-polyacylated amine bleach activators,
(b2) enzymes, and
(b3) fluorescers;
(c) one or more detergent-active compounds, one or more detergency builders, and optionally
other detergent ingredients;
(ii) compressing the powder to form a tablet in which ingredients (a) and (b) are
not segregated from one another.
12. A process as claimed in claim 11, wherein the sodium perborate (a) is present as sodium
perborate monohydrate and, wherein the detergent contains up to 60% by weight of alkali
metal aluminosilicate detergency builder.
13. A process as claimed in either claim 11 or claim 12, characterised by the steps of:
(i) spray-drying an aqueous slurry to form a base powder including one or more detergent-active
compounds and one or more detergency builders, any fluorescer (b3) to be included,
and other ingredients as desires;
(ii) admixing to the base powder the sodium perborate (a), any N-diacylated or N,N'-polyacylated
amine bleach activator (b1) and/or enzyme (b2) to be included, and optionally other
ingredients, as desired, to form a homogeneous powder;
(iii) compressing the powder to form a tablet.