CA1308374C - Detergent composition - Google Patents
Detergent compositionInfo
- Publication number
- CA1308374C CA1308374C CA000489502A CA489502A CA1308374C CA 1308374 C CA1308374 C CA 1308374C CA 000489502 A CA000489502 A CA 000489502A CA 489502 A CA489502 A CA 489502A CA 1308374 C CA1308374 C CA 1308374C
- Authority
- CA
- Canada
- Prior art keywords
- detergent
- cellulase
- clay
- compositions
- composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38645—Preparations containing enzymes, e.g. protease or amylase containing cellulase
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/02—Inorganic compounds ; Elemental compounds
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/126—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in solid compositions
Abstract
C.3044 A B S T R A C T
Fabric washing compositions containing a surfactant, which is usually an anionic and/or nonionic surfactant, and optionally other conventional ingredients such as builders, bleaches etc additionally contain both cellulase and a clay, particularly a smectite clay, to provide a softening benefit on cellulosic fabrics. The compositions may also contain cationic antistatic agents.
Fabric washing compositions containing a surfactant, which is usually an anionic and/or nonionic surfactant, and optionally other conventional ingredients such as builders, bleaches etc additionally contain both cellulase and a clay, particularly a smectite clay, to provide a softening benefit on cellulosic fabrics. The compositions may also contain cationic antistatic agents.
Description
~L3~37~
- 1 - C.3~44 DETERGENT COMPOSI~ION
.
This invention relates to deter~ent compositions for S washing fabrics, in particular to detergent compositions which are capable of cleaning and softening fabrics from the s,Ime wash liquo~.
Detergent compositions for simultaneously cleaning and softening fabrics are known in the art.
Conventionally such compositions contain, as a detergent active material, an anionic surfactant to clean the fabrics and a cationic fabric softening agent. However, there is a tendency for the anionic and cationic components of such compositions to react with each other, either in the product i~self or in the wash liquor, with the result that the efficiency of the cationic softening agent is significantly reduced.
Various solutions to this problem have been proposed~ One such proposal, as described in United States patent specification 3 936 537 (BASKERVILLE et al assigned to THE PROCTER~& GAMBLE COMPANY) is to combine .
- :
- 1 - C.3~44 DETERGENT COMPOSI~ION
.
This invention relates to deter~ent compositions for S washing fabrics, in particular to detergent compositions which are capable of cleaning and softening fabrics from the s,Ime wash liquo~.
Detergent compositions for simultaneously cleaning and softening fabrics are known in the art.
Conventionally such compositions contain, as a detergent active material, an anionic surfactant to clean the fabrics and a cationic fabric softening agent. However, there is a tendency for the anionic and cationic components of such compositions to react with each other, either in the product i~self or in the wash liquor, with the result that the efficiency of the cationic softening agent is significantly reduced.
Various solutions to this problem have been proposed~ One such proposal, as described in United States patent specification 3 936 537 (BASKERVILLE et al assigned to THE PROCTER~& GAMBLE COMPANY) is to combine .
- :
- 2 - C.30~4 the cationic components in a separate particle with a dispersion inhibitor, such as a long chain alkanol, with the object of reducing the interaction with the anionic surfactant in the wash liquor.
An alternative proposal is to avoid the use of anionic surfactants, by for example using nonionic surfactants as described in British Patent Specification GB 1 079 388 tGENERAL FOODS CORPORATION).
A further series of proposals relate to the us~ of alternative fabric softening agents in place of the cationic material. One such example is to use cellulolytic enzymes ie cellulase, as a harshness-reducing agent, as disclosed in British Patent Specification GB 1 368 599 (UNILEVER). Other enzymes, such as proteolytic enzymes like Alcalase, do not provide softening benefits. A further example is to use various clay materials as disclosed in United States patent specification US 4 062 647 ~STORM et al assigned to THE
PROCTER & GAMBLE COMPANY) .
To date, none of these various proposals bythemselves, have lead to commercially successful products.
It is thought that cellulase achieves its anti~
harshening effect on eg cotton, by cleaving and thereby assisting the removal of the cellulosic fibrils which form on the fabric fibres in the normal washing process, the bonding of these fibrils to each other and the cotton fibres themselves being responsible for introducing a degree of rigidity, that is harshening, to the fabric surface. On the other hand it is believed that clay materials achieve their softening benefit by coating the fibres and fibrils with a layer o~ lubricating material thereby lowering the friction between fibrils and - 3 - C.3044 fibrils/fibres reducing the tendency of the fibril~ ~o bond together. One would expect therefor2 that where a composition contains cellulase as a fabric softening agent, there is nothing to be gained from the additional inclusion of clay materials, the fibrils having been removed following cellulase action. Looking at *he matter in another manner, one would expect that where a composition contains a clay material as a softening agent, there is no~hing to be yained rom the additional inclusion of ~ellulase, the clay coating on the fibrils effectively screening the fibrils from attack by the callulase, which is known to be selective towards cellulosic matexial~ and not in any way to attack clay materials~
For this reason one would expect that in compo~itions which contain both cellulase and clay materials, these softening agents would appear to mutually inhibit one another and we believe it i3 for this reason that compo~itions containing both cellulase and clay materials as softening agents have not previously been proposed.
We have now surprisingly discovered however ~hat this mutual inhibition does not occur in practice and that therefore fabric washing compositions which contain both cellulase and clay materials aq softening agents provide qurprisingly good softening results.
Thus, according to the invention, there i5 provided a detergent composition for cleaning and softening fabrics comprising:
.
( i) 5 to 50% of a detergent active material;
_ 4 _ C.304~
( ii) 1.5 to 35~ of a fabric softening clay material, and (iii) 0.1 to 10~ of cellulase.
We are aware of British patent specification Nos.
2 094 826, 2 095 275 and 2 124 244 fKA0 SOAP) which disclose detergent compositions which contain specific types of cellulase to provide improved detergency. In these specifications clay, of unspecified type, is mentioned as an ingredient for inhibiting caking of the compo6itions.
The compositions according to the invention necessarily contain a detergent active material, otherwise referred to herein simply as a detergent compound. The detergent compounds may be selected from anionic, nonionic, zwitterionic and amphoteric synthetic detergent active materials. ~any suitable detergent compounds are commercially 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.
The preferred detergent compounds which can be used are synthetic anionic and nonionic compounds. The former are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals. Examples of suitable synthetic anionic detergent compound~ are sodium and potassium alkyl sulphate~, especially those obtained by sulphating higher tC8-C18 ) alcohols produced for example from tallow or coconut oil, sodium and potas~ium alkyl (Cg-C20) benzene sulphonates, particularly sodium linear secondary alkyl (Clo-C15) benzene sulphonates; sodium alkyl glyceryl ether :
, .
D8~
- 5 - C.30~4 sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monogl~ceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C8-C18) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esteri~ied with isethionic acid and neutralised with sodium hydroxide;
sodium and potassium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha-olefins (C8-C20) with sodium bisulphite and those derived from reacting paraffins with S02 and C12 and then hydrolysing with a base to produce a random sulphonate; and olefin sulphonates, which term is used to describe the material made by reacting olefins, particularly C10-C20 alpha-olefins, with S03 and then neutralising and hydrolysing the reaction product. The preferred anionic detergent compounds are sodium (Cll-C15) alkyl benzene sulphonates and sodium (C16-C18) alkyl sulphates.
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 al~ylene oxides, especially ethylene oxide either alone or with propylene oxide.
Specific nonionic detergent compounds are alkyl (C6-C22) phenols-ethylene oxide condensates, generally 5 to 25 EO, ie 5 to 25 units of ethylene oxide per molecule, the condensation products of aliphatic (C8-C18) primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Other so-called nonionic 3~L
- 6 - C.3044 detergent compounds include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
Mixtures of detergent compounds, for example mixed anionic or mixed anionic and nonionic compounds may be used in the detergent compositions, particularly in the latter case to provide controlled low sudsing properties.
This is beneficial for compositions intended for use in suds-intolerant automatic washing machines.
Amounts of amphoteric or zwitterionic detergent compounds can also be used in the compositions of the invention but this i5 not normally desired due to their relatively high cost. If any amphoteric or zwitterionic detergent compounds are used it is generally in small amounts in compositions based on the much more commonly used synthetic anionic and/or nonionic detergent compounds.
The effective amount of the detergent active compound or compounds used in the composition of the present invention is generally in the range of from 2 to 50~, preferably from 5 to 40~ by weight, most preferably not more than 30% by weight of the composition.
A second essential component of the compositions of the present invention is a fabric softening clay material.
This clay material should be a phyllosilicate clay with a 2:1 layer structure, which definition includes pyrophyllite clays, smectite or montmorillonite clays, saponites, vermiculites and micas. Clay materials which have been found to be unsuitable for fabric softening purposes include chlorites and kaolinites. Other aluminosilicate materials which do not have a layer structure, such as zeolites are also unsuitable as fabric ;3 s)~
- 7 - C.3044 softening clay materials. Particularly suitable clay materials are the smectite clays described in detail in United States Patent Specification US 3 959 155 (MONTGOMERY
et al assigned to THE PROCTER & GAMBLE COMPANY), especially smectite clays such as described in United States Patent Specification US 3 936 537 (BASKE~VILLE - referred to above). Other disclosures of suitable clay materials for fabric softening purposes include European patent specification EP 26528-A (PROCTER & GAMBLE LIMITED).
The most preferred clay fabric softening materials include those materials of bentonitic origin, bentonites being primarily montmorillonite type clays together with various impurities, the level and nature of which depends on the source of the clay material.
The level of fabric softening clay material in the compositions of the invention should be sufficient to provide the fabrics with a softening benefit. A preferred level is 1.5~ to 35% by weight of the composition, most preferably from 4% to 15%, these percentages referring to the level of the clay mineral er se. Levels of clay raw material higher than this may be necessary when the raw material is derived from a particularly impure source.
A third essential component of the compositions of the invention is the cellulase.
The cellulase in the present invention may be any bacterial or fungal cellulase having a pH optimum of between 5 and 11.5. It is however preferred to use cellulases which have optimum activity at alkaline p~
values, such as those described in British Patent ~`
, - 8 - C.30~4 Specifications GB 2 075 028 A (NOVO INDUSTRIE A/S~, GB 2 095 275 A (KAO SOAP CO LTD~ and GB 2 094 826 A (KAO
SOAP CO LTD).
Examples of such alkaline cellulases are cellulases produced by a strain of ~umicola insolens (Humicola grisea var. thermoidea), particularly the Humicola strain DSM
1800, and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging to the genus Aeromonas, and cellulase ex~racted from the hepatopancreas of a marine mullosc (Dolabella Auricula Solander).
The cellulase added to the composition o~ the invention may be in the form of a non-dusting granulate, eg "marumes" or "prill~", or in the form of a liquid in whi~h the cellulase is provided as a cellulase concentrate suspended in eg a nonionic surfactant or dissolved in an aqueous medium, having cellulase activity of at least 250 regular Cx cellulase activity units/gram, measured under the standard conditions as described in GB 2 075 028 A~
The amount of cellulase in the composition of the invention will, in general, be from about 0.1 to 10% by weight in whatever form. In terms of cellulase activity the use of cellulase in an amount corresponding to from 0.25 to 150 or higher regular Cx units/gram of the detergent composition is within the preferred scope of the present invention. A most preferred range of cellulase activity, however, is from 0.5 to 25 regular Cx units/gram of the detergent composition.
The compositions of the invention will generally include a detergency builder to improve the efficiency of the detergent active, in particular to remove calcium hardness ions from the water and to provide alkalinity.
The builder material may be selected from precipitating _ g _ C.3044 builder materials (such as alkali metal carbonates, bicarbonates, borates, orthophosphates and silicates), sequestering builder materials (such as alkali metal pyrophosphates, polyphosphates, amino polyacetates, phytates, polyphosphonates, aminopolymethylene phosphonates and polycarboxylates), ion-exchange builder materials (such as zeolites and amorphous alumino-silicates), or mixtures of any one or more of these materials. Preferred examples of builder matPrials include sodium tripolyphosphate, mix~ures thereof with sodium orthophosphate, sodium carbonate, mixtures thereof with calcite as a seed crystal, sodium citrate, zeolite and the sodium salt of nitrilotriacetic acid.
The level of builder material in the compositions of the invention may be up to 80% by weight, p,referably from 20~ to 70% by weight and most preferably from 30~ to 60%
by weight.
Apart from the components already mentioned, a detergent composition of the invention can contain any of the conventional additives in the amounts in which such additives are normally employed in fabric washing detergent compositions. Examples of these additives include the lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel atty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine-releasing bleaching agents such as tricloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, 1uorescent agents, perfumes, other enzymes such as proteases and amylases, qermicides and colourants.
- 10 - C.3044 We have found it particularly beneficial to include in the compositions of the invention an antistatic agent, to reduce the level of static on washed fabrics, especially those fabrics which include synthetic fibres, S such as nylon.
The antistatic agents useful herein are quaternary ammonium salts of the formula ~RlR2R3R4N] Y wherein at least one, but not more than two, of Rl, R2, R3 and R~ is an organic radical containing a group selected from a C16-C22 aliphatic radical, or an alkyl phenyl or alkyl benzyl radical having 10-16 atoms in the alkyl chain, the remaining group or groups being selected from hydrocarbyl groups containing from 1 to about 4 carbon atoms, or C2 C4 hydroxy alkyl groups and cyclic structures in which the nitrogen atom forms part of the ring, and Y is an anion such as halide, methylsulfate, or ethylsulfate.
In the context of the above definition, the hydrophobic moiety (ie, the C16-C22 aliphatic, Cl~-C16 alkyl phenyl or alkyl benzyl radical) in the organic radical Rl may be directly attached to the quaternary nitrogen atom or may be indirectly attached thereto through an amide, esters, alkoxy, e~her, or like grouping.
The quaternary ammonium antistatic agents can be prepared in various ways well known in the art. Many such materials are commercially available. The quaternaries are often made from alkyl halide mixtures corresponding to the mixed alkyl chain lengths in fatty acids. For example, the "ditallown quaternaries are made from alkyl halides having mixed C14-C18 chain lengths.
Such mixed di-long chain quaternaries are useful herein and are preferred from a cost standpoint. Optionally, the tallow alkyl groups are hydrogenated or "hardened" to reduce the level of unsaturation and thereby raise the - 11 - C.3044 melting point and lower the water-solubility of compounds made therefrom. As used herein "ditallow" is intended to refer to the above-described ditallowalkyl quaternaries, either in their hardened or unhardened forms.
The quaternary ammonium antistatic compounds useful herein include both water-soluble and substantially water-insoluble materials. Imidazolinium compounds enumerated in US 3 936 537 (BASKERVILLE - referred to above) possess appreciable water solubility and are preferably utilised in the pxesent invention by mixing with an appropriate type and level of organic dispersion inhibitor and complexing component to give ultimate particle solubility in water of less than 50 ppm lParts per million~ at 25C. Relatively water-soluble quaternary ammonium antistatic agents may also be of the nonring variety, such as diisostearyl dimethyl ammonium chlorides. Exempl~ry quatexnary ammonium imidazolinium compounds are specifically methyl-l-alkylamidoethyl-2-alkyl imidazolinium methyl sulfates, specificallyl-methyl-l-[(tallowamido)ethyl]-2-tallowimidazolinium methyl sulfate. However, the most useful quaternary ammonium antistatic agents are characterised by relatively limited solubility in water.
The following are representative examples of substantially water-insoluble quaternary ammonium antistatic agents suitable for use in the compositions of the instan~ invention. Dioctadecyldimethyl ammonium chloride is an especially preferred quaternary antistatic agent for use herein by virtue of its high antistatic activity; ditallow dimethyl ammonium chloride is equally preferred because of its ready availability and its good antistatic activity; other useful di-long chain quaternary compounds are dicetyl dimethyl ammonium chloride;
bis-docosyl dimethyl ammonium chloride; didodecyl dimethyl .
- 12 - C.3044 ammonium chloride; ditallow dimethyl ammonium bromide;
dioleyoyl dimethyl ammonium hydroxide; ditallow dimethyl ammonium chloride; ditallow dipropyl ammonium bromide;
ditallow dibutyl ammonium fluoride; cetyldecylmethylethyl ammonium chloride; bis-[ditallow dimethyl ammonium~
sulfate; and tris [ditallow dimethyl ammonium] phosphate.
The level of cationic antistatic agent should be sufficien~ to provide an antistatic benefit on synthetic fabrics. We have found that at least 1.0% by weight, most preferably at least 1.5% by weight of cationic antistatic agent is suitable. The compositions of the invention need not contain more than 10~ by weight, generally not more than 6% by weight antistatic agent.
The compositions of the invention may also include organic amines. Suitable amines include primary, secondary and tertiary amines, such as hydrogenated tallow alkyl primary amine, secondary coconut methyl amine or methyl di-hardened tallow alkyl tertiary amine. The presence of such amines in the composition is known to enhance the perfume delivery to the fabrics. A suitable level for the amine in the composi~ion is from 1.0% to 10%, most preferably 1.5% to 6% by weight.
PREPARATION OF THE COMPOSI~ION
The detergent compositions may be prepared in any way appropriate to their physical form such as by -dry-mixing the components, co agglomerating them or dispersing them in a liquid carrier. However, a preferred physical form is a granule incorporating a deterg ncy builder material and this is most conveniently manufactured by spray-drying at least part of the composition.
' .
' ` ',' .
`` ~ 7~
- 13 - C.304~
The preferred compositions of the invention may be prepared by making up an aqueous slurry of the non-heat-sensitive component~, comprising the anionic and/or nonionic surfactants, the clay-fabric softening material, the builder and filler salts together with any soil-suspending agents and optical brighteners, and spray-drying this slurry. The moisture content of the slurry is normally in the range of 28% to 35% and its temperature is conveniently in the range of 70C-95C.
The spray-drying tower inlet temperatures are normally in the range of 300-360C and the resultant spray-dried granules have a moisture content of 8-12% by weight. An optional, but preferred, additional processing step i5 to cool the dried granules rapidly by means of cool air from a temperature o 90C to a temperature in the range of 25-35C, in order to facilitate the further processing of the product. Solid heat-sensitive components, such as persalts and enzymes, are mixed with the spray-dried granules. Although ~he cationic antistatic agent, if 2Q any, may be included in the slurry for spray-drying, this component may degrade under certain processing conditions and adversely affect product quality. It is therefore preferred that the antistatic agent if any be liquefied by melting or solvent dissolution and that this liquid be sprayed onto the spray-dried granules before or after other heat-sensitive solids have been dry-mixed with them.
If the antistatic agent is applied as a melt, a liquid temperature of 5-30C in excess of the melting point can conveniently be used for the spray-on. When the antistatic agent is a waxy solid of rather low melting point, it may be blended with a compatible higher melting substance so as to ensure that granules sprayed on therewith are sufficiently crisp, are free-flowing and do not cake on storage. It is also possible to add the clay material as a granule, together with the solid heat-sensitive components to ~he spray-dried granules.
- 1~ - C.30~4 The invention is illustrated by the following non-limiting examples.
A detergent composition was prepared by spray-drying the following components:
Alkyl benzene sulphonate 5.5 Ethoxylated alcohol 3.0~
Soap 2.0%
Sodium tripolyphosphate 30.0%
Sodium silicate 5.0%
Sodium sulphate 8.0%
Water and minor ingredients 11.5%
where the percentages quoted are based on the weight of the final product. To this spray-dried base powder was added 21.0~ of sodium perborate tetrahydrate and 14%
sodium sulphate. This composition was used as a control.
Further compositions were prepared which included various amounts of clay and cellulase as set out below. These components were added to the spray dried base powder granules and the level of post-dosed sodium sulphate in the base powder was reduced accordingly.
Example No: Control A B C _ 1 2 Cellulase - 0.55%* 3.3%** - 0.55%* 3.3%**
Clay - - - 10% 10% 10~
* Cellulase added to give 10 Cx units/l in the wash (pH 9.3)~
** Cellulase added to give 60 Cx units/l in the wash (pH 9.3).
:
.
. , ' ' .
, ` ' , "' .
- 15 - C.3044 These compositions were then used to wash pre-harshened terry towelling monitors. The product dosage was 5 g/l, the water hardness was 8GH equivalent to about 1.36xlO 3molar free calcium ions and the pH of the wash liquor was approximately 9.~ IELE (Trade Mark) automatic washing machine was used on a 25C to 40C heat up cycle, heating up at 2C/min. The wash time was 35 minutes. After washing the monitors were rinsed 3 times in tap water. After 5 washes the monitors were line-dried and then assessed for softness using a laboratory fabric softness measuring device. ~he results were as set out in the following Table, the softness of the monitors washed once in the control formulation being taken as 100%.
Example No % softness after 5 washes Control (after 1 wash) 100 Control (after 5 washes3 103 A comparison of the results obtained from all compositions relative to the control shows that both cellulase and clay improve the measured softening. A
comparison of the results obtained from compositions A, C
and Example 1 shows that the use of clay and cellulase together gives a softening benefit which is greater than the use of either softening component alone. A similar conclusion can be drawn from a comparison of compositions B, C and Example 2.
- 16 - C.30~4 The cellulase used in these compositions was a granulated ~umicola insolens cellulase SP 227 ex NOVO
having an activity at pH 9,3 of 365 Cx units/gram. The clay used in these compositions was White Bentonite from ~urkey, available from Steetley Minerals ~imited, England which consists of about 95% clay mineral and has a cation exchange capacity of between 90 and 100 meqllOO g.
Similar results are obtained when additionally 4~ by weight of diharde~ed tallow dimethyl ammonium chloride ~AROSURF TA 100 - Trade Mark) are included as an antistatic agent, and antistatic test~ on synthetic fabrics show a significant benefit over those compositions where no antistatic agent is present. ~lso, similar benefits for the combination of clay and cellulase occur when the phosphate containing base referred to above is replaced with a base containing zeolite and sodium carbonate but no phosphate.
Using the same spray-dried base powder used in Examples 1 and 2, compositions were prepared having the following formulations (% by weight).
.
~L3~3~
- 17 - C.3044 Example No: Control D E 3 F ~ 4 Base powder65 65 65 65 65 65 65 Clay - l - 10 10 10 Clay - 2 ~ 10 10 10 Cellulase - - - 1.0* - - 1.0*
Alcalase - - 0.21**- - 0~21**-Sodium perborate 21 2121 21 21 21 21 Sodium sulphate ---------- balance to 100% ~
* Cellulase added to give 10 Cx units/l in the wash ** Alcalase added to give 10 gU/ml in the wash Clay No. 1 is a bentonite having a cation exchange capacity of 95 meg/lOOg while Clay No~ 2 is a bentonite having a cation exchange capacity of 31 meg/lOOg Using the same evaluation method as described in connection with Examples 1 and 2 the softness of terry towelling monitors was assessed and the results were as ~ollows:
~5 Example No: Control D E 3 F G 4 % sotness 100 106 104 113 105 103 107 These results demonstrate that in the case of clay No. 1, in comparison with the Control, the presence of clay improves softening lExample D) and this softening is further improved by the additional presence of cellulase (Example 3) but not by the additional presence of alcalase (Example E). The same conclusion can be drawn from the results of those Examples which contain Clay No. 2.
lExamples F, G and 4). It is also apparent from these results that Clay No. 1 shows improved results over Clay No. 2, particularly in the presence of cellula~e (compare Examples 3 and 4 ) .
..
An alternative proposal is to avoid the use of anionic surfactants, by for example using nonionic surfactants as described in British Patent Specification GB 1 079 388 tGENERAL FOODS CORPORATION).
A further series of proposals relate to the us~ of alternative fabric softening agents in place of the cationic material. One such example is to use cellulolytic enzymes ie cellulase, as a harshness-reducing agent, as disclosed in British Patent Specification GB 1 368 599 (UNILEVER). Other enzymes, such as proteolytic enzymes like Alcalase, do not provide softening benefits. A further example is to use various clay materials as disclosed in United States patent specification US 4 062 647 ~STORM et al assigned to THE
PROCTER & GAMBLE COMPANY) .
To date, none of these various proposals bythemselves, have lead to commercially successful products.
It is thought that cellulase achieves its anti~
harshening effect on eg cotton, by cleaving and thereby assisting the removal of the cellulosic fibrils which form on the fabric fibres in the normal washing process, the bonding of these fibrils to each other and the cotton fibres themselves being responsible for introducing a degree of rigidity, that is harshening, to the fabric surface. On the other hand it is believed that clay materials achieve their softening benefit by coating the fibres and fibrils with a layer o~ lubricating material thereby lowering the friction between fibrils and - 3 - C.3044 fibrils/fibres reducing the tendency of the fibril~ ~o bond together. One would expect therefor2 that where a composition contains cellulase as a fabric softening agent, there is nothing to be gained from the additional inclusion of clay materials, the fibrils having been removed following cellulase action. Looking at *he matter in another manner, one would expect that where a composition contains a clay material as a softening agent, there is no~hing to be yained rom the additional inclusion of ~ellulase, the clay coating on the fibrils effectively screening the fibrils from attack by the callulase, which is known to be selective towards cellulosic matexial~ and not in any way to attack clay materials~
For this reason one would expect that in compo~itions which contain both cellulase and clay materials, these softening agents would appear to mutually inhibit one another and we believe it i3 for this reason that compo~itions containing both cellulase and clay materials as softening agents have not previously been proposed.
We have now surprisingly discovered however ~hat this mutual inhibition does not occur in practice and that therefore fabric washing compositions which contain both cellulase and clay materials aq softening agents provide qurprisingly good softening results.
Thus, according to the invention, there i5 provided a detergent composition for cleaning and softening fabrics comprising:
.
( i) 5 to 50% of a detergent active material;
_ 4 _ C.304~
( ii) 1.5 to 35~ of a fabric softening clay material, and (iii) 0.1 to 10~ of cellulase.
We are aware of British patent specification Nos.
2 094 826, 2 095 275 and 2 124 244 fKA0 SOAP) which disclose detergent compositions which contain specific types of cellulase to provide improved detergency. In these specifications clay, of unspecified type, is mentioned as an ingredient for inhibiting caking of the compo6itions.
The compositions according to the invention necessarily contain a detergent active material, otherwise referred to herein simply as a detergent compound. The detergent compounds may be selected from anionic, nonionic, zwitterionic and amphoteric synthetic detergent active materials. ~any suitable detergent compounds are commercially 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.
The preferred detergent compounds which can be used are synthetic anionic and nonionic compounds. The former are usually water-soluble alkali metal salts of organic sulphates and sulphonates having alkyl radicals containing from about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals. Examples of suitable synthetic anionic detergent compound~ are sodium and potassium alkyl sulphate~, especially those obtained by sulphating higher tC8-C18 ) alcohols produced for example from tallow or coconut oil, sodium and potas~ium alkyl (Cg-C20) benzene sulphonates, particularly sodium linear secondary alkyl (Clo-C15) benzene sulphonates; sodium alkyl glyceryl ether :
, .
D8~
- 5 - C.30~4 sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty monogl~ceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C8-C18) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esteri~ied with isethionic acid and neutralised with sodium hydroxide;
sodium and potassium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha-olefins (C8-C20) with sodium bisulphite and those derived from reacting paraffins with S02 and C12 and then hydrolysing with a base to produce a random sulphonate; and olefin sulphonates, which term is used to describe the material made by reacting olefins, particularly C10-C20 alpha-olefins, with S03 and then neutralising and hydrolysing the reaction product. The preferred anionic detergent compounds are sodium (Cll-C15) alkyl benzene sulphonates and sodium (C16-C18) alkyl sulphates.
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 al~ylene oxides, especially ethylene oxide either alone or with propylene oxide.
Specific nonionic detergent compounds are alkyl (C6-C22) phenols-ethylene oxide condensates, generally 5 to 25 EO, ie 5 to 25 units of ethylene oxide per molecule, the condensation products of aliphatic (C8-C18) primary or secondary linear or branched alcohols with ethylene oxide, generally 5 to 40 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Other so-called nonionic 3~L
- 6 - C.3044 detergent compounds include long chain tertiary amine oxides, long chain tertiary phosphine oxides and dialkyl sulphoxides.
Mixtures of detergent compounds, for example mixed anionic or mixed anionic and nonionic compounds may be used in the detergent compositions, particularly in the latter case to provide controlled low sudsing properties.
This is beneficial for compositions intended for use in suds-intolerant automatic washing machines.
Amounts of amphoteric or zwitterionic detergent compounds can also be used in the compositions of the invention but this i5 not normally desired due to their relatively high cost. If any amphoteric or zwitterionic detergent compounds are used it is generally in small amounts in compositions based on the much more commonly used synthetic anionic and/or nonionic detergent compounds.
The effective amount of the detergent active compound or compounds used in the composition of the present invention is generally in the range of from 2 to 50~, preferably from 5 to 40~ by weight, most preferably not more than 30% by weight of the composition.
A second essential component of the compositions of the present invention is a fabric softening clay material.
This clay material should be a phyllosilicate clay with a 2:1 layer structure, which definition includes pyrophyllite clays, smectite or montmorillonite clays, saponites, vermiculites and micas. Clay materials which have been found to be unsuitable for fabric softening purposes include chlorites and kaolinites. Other aluminosilicate materials which do not have a layer structure, such as zeolites are also unsuitable as fabric ;3 s)~
- 7 - C.3044 softening clay materials. Particularly suitable clay materials are the smectite clays described in detail in United States Patent Specification US 3 959 155 (MONTGOMERY
et al assigned to THE PROCTER & GAMBLE COMPANY), especially smectite clays such as described in United States Patent Specification US 3 936 537 (BASKE~VILLE - referred to above). Other disclosures of suitable clay materials for fabric softening purposes include European patent specification EP 26528-A (PROCTER & GAMBLE LIMITED).
The most preferred clay fabric softening materials include those materials of bentonitic origin, bentonites being primarily montmorillonite type clays together with various impurities, the level and nature of which depends on the source of the clay material.
The level of fabric softening clay material in the compositions of the invention should be sufficient to provide the fabrics with a softening benefit. A preferred level is 1.5~ to 35% by weight of the composition, most preferably from 4% to 15%, these percentages referring to the level of the clay mineral er se. Levels of clay raw material higher than this may be necessary when the raw material is derived from a particularly impure source.
A third essential component of the compositions of the invention is the cellulase.
The cellulase in the present invention may be any bacterial or fungal cellulase having a pH optimum of between 5 and 11.5. It is however preferred to use cellulases which have optimum activity at alkaline p~
values, such as those described in British Patent ~`
, - 8 - C.30~4 Specifications GB 2 075 028 A (NOVO INDUSTRIE A/S~, GB 2 095 275 A (KAO SOAP CO LTD~ and GB 2 094 826 A (KAO
SOAP CO LTD).
Examples of such alkaline cellulases are cellulases produced by a strain of ~umicola insolens (Humicola grisea var. thermoidea), particularly the Humicola strain DSM
1800, and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging to the genus Aeromonas, and cellulase ex~racted from the hepatopancreas of a marine mullosc (Dolabella Auricula Solander).
The cellulase added to the composition o~ the invention may be in the form of a non-dusting granulate, eg "marumes" or "prill~", or in the form of a liquid in whi~h the cellulase is provided as a cellulase concentrate suspended in eg a nonionic surfactant or dissolved in an aqueous medium, having cellulase activity of at least 250 regular Cx cellulase activity units/gram, measured under the standard conditions as described in GB 2 075 028 A~
The amount of cellulase in the composition of the invention will, in general, be from about 0.1 to 10% by weight in whatever form. In terms of cellulase activity the use of cellulase in an amount corresponding to from 0.25 to 150 or higher regular Cx units/gram of the detergent composition is within the preferred scope of the present invention. A most preferred range of cellulase activity, however, is from 0.5 to 25 regular Cx units/gram of the detergent composition.
The compositions of the invention will generally include a detergency builder to improve the efficiency of the detergent active, in particular to remove calcium hardness ions from the water and to provide alkalinity.
The builder material may be selected from precipitating _ g _ C.3044 builder materials (such as alkali metal carbonates, bicarbonates, borates, orthophosphates and silicates), sequestering builder materials (such as alkali metal pyrophosphates, polyphosphates, amino polyacetates, phytates, polyphosphonates, aminopolymethylene phosphonates and polycarboxylates), ion-exchange builder materials (such as zeolites and amorphous alumino-silicates), or mixtures of any one or more of these materials. Preferred examples of builder matPrials include sodium tripolyphosphate, mix~ures thereof with sodium orthophosphate, sodium carbonate, mixtures thereof with calcite as a seed crystal, sodium citrate, zeolite and the sodium salt of nitrilotriacetic acid.
The level of builder material in the compositions of the invention may be up to 80% by weight, p,referably from 20~ to 70% by weight and most preferably from 30~ to 60%
by weight.
Apart from the components already mentioned, a detergent composition of the invention can contain any of the conventional additives in the amounts in which such additives are normally employed in fabric washing detergent compositions. Examples of these additives include the lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel atty acids and coconut fatty acids, lather depressants, oxygen-releasing bleaching agents such as sodium perborate and sodium percarbonate, peracid bleach precursors, chlorine-releasing bleaching agents such as tricloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually present in very minor amounts, 1uorescent agents, perfumes, other enzymes such as proteases and amylases, qermicides and colourants.
- 10 - C.3044 We have found it particularly beneficial to include in the compositions of the invention an antistatic agent, to reduce the level of static on washed fabrics, especially those fabrics which include synthetic fibres, S such as nylon.
The antistatic agents useful herein are quaternary ammonium salts of the formula ~RlR2R3R4N] Y wherein at least one, but not more than two, of Rl, R2, R3 and R~ is an organic radical containing a group selected from a C16-C22 aliphatic radical, or an alkyl phenyl or alkyl benzyl radical having 10-16 atoms in the alkyl chain, the remaining group or groups being selected from hydrocarbyl groups containing from 1 to about 4 carbon atoms, or C2 C4 hydroxy alkyl groups and cyclic structures in which the nitrogen atom forms part of the ring, and Y is an anion such as halide, methylsulfate, or ethylsulfate.
In the context of the above definition, the hydrophobic moiety (ie, the C16-C22 aliphatic, Cl~-C16 alkyl phenyl or alkyl benzyl radical) in the organic radical Rl may be directly attached to the quaternary nitrogen atom or may be indirectly attached thereto through an amide, esters, alkoxy, e~her, or like grouping.
The quaternary ammonium antistatic agents can be prepared in various ways well known in the art. Many such materials are commercially available. The quaternaries are often made from alkyl halide mixtures corresponding to the mixed alkyl chain lengths in fatty acids. For example, the "ditallown quaternaries are made from alkyl halides having mixed C14-C18 chain lengths.
Such mixed di-long chain quaternaries are useful herein and are preferred from a cost standpoint. Optionally, the tallow alkyl groups are hydrogenated or "hardened" to reduce the level of unsaturation and thereby raise the - 11 - C.3044 melting point and lower the water-solubility of compounds made therefrom. As used herein "ditallow" is intended to refer to the above-described ditallowalkyl quaternaries, either in their hardened or unhardened forms.
The quaternary ammonium antistatic compounds useful herein include both water-soluble and substantially water-insoluble materials. Imidazolinium compounds enumerated in US 3 936 537 (BASKERVILLE - referred to above) possess appreciable water solubility and are preferably utilised in the pxesent invention by mixing with an appropriate type and level of organic dispersion inhibitor and complexing component to give ultimate particle solubility in water of less than 50 ppm lParts per million~ at 25C. Relatively water-soluble quaternary ammonium antistatic agents may also be of the nonring variety, such as diisostearyl dimethyl ammonium chlorides. Exempl~ry quatexnary ammonium imidazolinium compounds are specifically methyl-l-alkylamidoethyl-2-alkyl imidazolinium methyl sulfates, specificallyl-methyl-l-[(tallowamido)ethyl]-2-tallowimidazolinium methyl sulfate. However, the most useful quaternary ammonium antistatic agents are characterised by relatively limited solubility in water.
The following are representative examples of substantially water-insoluble quaternary ammonium antistatic agents suitable for use in the compositions of the instan~ invention. Dioctadecyldimethyl ammonium chloride is an especially preferred quaternary antistatic agent for use herein by virtue of its high antistatic activity; ditallow dimethyl ammonium chloride is equally preferred because of its ready availability and its good antistatic activity; other useful di-long chain quaternary compounds are dicetyl dimethyl ammonium chloride;
bis-docosyl dimethyl ammonium chloride; didodecyl dimethyl .
- 12 - C.3044 ammonium chloride; ditallow dimethyl ammonium bromide;
dioleyoyl dimethyl ammonium hydroxide; ditallow dimethyl ammonium chloride; ditallow dipropyl ammonium bromide;
ditallow dibutyl ammonium fluoride; cetyldecylmethylethyl ammonium chloride; bis-[ditallow dimethyl ammonium~
sulfate; and tris [ditallow dimethyl ammonium] phosphate.
The level of cationic antistatic agent should be sufficien~ to provide an antistatic benefit on synthetic fabrics. We have found that at least 1.0% by weight, most preferably at least 1.5% by weight of cationic antistatic agent is suitable. The compositions of the invention need not contain more than 10~ by weight, generally not more than 6% by weight antistatic agent.
The compositions of the invention may also include organic amines. Suitable amines include primary, secondary and tertiary amines, such as hydrogenated tallow alkyl primary amine, secondary coconut methyl amine or methyl di-hardened tallow alkyl tertiary amine. The presence of such amines in the composition is known to enhance the perfume delivery to the fabrics. A suitable level for the amine in the composi~ion is from 1.0% to 10%, most preferably 1.5% to 6% by weight.
PREPARATION OF THE COMPOSI~ION
The detergent compositions may be prepared in any way appropriate to their physical form such as by -dry-mixing the components, co agglomerating them or dispersing them in a liquid carrier. However, a preferred physical form is a granule incorporating a deterg ncy builder material and this is most conveniently manufactured by spray-drying at least part of the composition.
' .
' ` ',' .
`` ~ 7~
- 13 - C.304~
The preferred compositions of the invention may be prepared by making up an aqueous slurry of the non-heat-sensitive component~, comprising the anionic and/or nonionic surfactants, the clay-fabric softening material, the builder and filler salts together with any soil-suspending agents and optical brighteners, and spray-drying this slurry. The moisture content of the slurry is normally in the range of 28% to 35% and its temperature is conveniently in the range of 70C-95C.
The spray-drying tower inlet temperatures are normally in the range of 300-360C and the resultant spray-dried granules have a moisture content of 8-12% by weight. An optional, but preferred, additional processing step i5 to cool the dried granules rapidly by means of cool air from a temperature o 90C to a temperature in the range of 25-35C, in order to facilitate the further processing of the product. Solid heat-sensitive components, such as persalts and enzymes, are mixed with the spray-dried granules. Although ~he cationic antistatic agent, if 2Q any, may be included in the slurry for spray-drying, this component may degrade under certain processing conditions and adversely affect product quality. It is therefore preferred that the antistatic agent if any be liquefied by melting or solvent dissolution and that this liquid be sprayed onto the spray-dried granules before or after other heat-sensitive solids have been dry-mixed with them.
If the antistatic agent is applied as a melt, a liquid temperature of 5-30C in excess of the melting point can conveniently be used for the spray-on. When the antistatic agent is a waxy solid of rather low melting point, it may be blended with a compatible higher melting substance so as to ensure that granules sprayed on therewith are sufficiently crisp, are free-flowing and do not cake on storage. It is also possible to add the clay material as a granule, together with the solid heat-sensitive components to ~he spray-dried granules.
- 1~ - C.30~4 The invention is illustrated by the following non-limiting examples.
A detergent composition was prepared by spray-drying the following components:
Alkyl benzene sulphonate 5.5 Ethoxylated alcohol 3.0~
Soap 2.0%
Sodium tripolyphosphate 30.0%
Sodium silicate 5.0%
Sodium sulphate 8.0%
Water and minor ingredients 11.5%
where the percentages quoted are based on the weight of the final product. To this spray-dried base powder was added 21.0~ of sodium perborate tetrahydrate and 14%
sodium sulphate. This composition was used as a control.
Further compositions were prepared which included various amounts of clay and cellulase as set out below. These components were added to the spray dried base powder granules and the level of post-dosed sodium sulphate in the base powder was reduced accordingly.
Example No: Control A B C _ 1 2 Cellulase - 0.55%* 3.3%** - 0.55%* 3.3%**
Clay - - - 10% 10% 10~
* Cellulase added to give 10 Cx units/l in the wash (pH 9.3)~
** Cellulase added to give 60 Cx units/l in the wash (pH 9.3).
:
.
. , ' ' .
, ` ' , "' .
- 15 - C.3044 These compositions were then used to wash pre-harshened terry towelling monitors. The product dosage was 5 g/l, the water hardness was 8GH equivalent to about 1.36xlO 3molar free calcium ions and the pH of the wash liquor was approximately 9.~ IELE (Trade Mark) automatic washing machine was used on a 25C to 40C heat up cycle, heating up at 2C/min. The wash time was 35 minutes. After washing the monitors were rinsed 3 times in tap water. After 5 washes the monitors were line-dried and then assessed for softness using a laboratory fabric softness measuring device. ~he results were as set out in the following Table, the softness of the monitors washed once in the control formulation being taken as 100%.
Example No % softness after 5 washes Control (after 1 wash) 100 Control (after 5 washes3 103 A comparison of the results obtained from all compositions relative to the control shows that both cellulase and clay improve the measured softening. A
comparison of the results obtained from compositions A, C
and Example 1 shows that the use of clay and cellulase together gives a softening benefit which is greater than the use of either softening component alone. A similar conclusion can be drawn from a comparison of compositions B, C and Example 2.
- 16 - C.30~4 The cellulase used in these compositions was a granulated ~umicola insolens cellulase SP 227 ex NOVO
having an activity at pH 9,3 of 365 Cx units/gram. The clay used in these compositions was White Bentonite from ~urkey, available from Steetley Minerals ~imited, England which consists of about 95% clay mineral and has a cation exchange capacity of between 90 and 100 meqllOO g.
Similar results are obtained when additionally 4~ by weight of diharde~ed tallow dimethyl ammonium chloride ~AROSURF TA 100 - Trade Mark) are included as an antistatic agent, and antistatic test~ on synthetic fabrics show a significant benefit over those compositions where no antistatic agent is present. ~lso, similar benefits for the combination of clay and cellulase occur when the phosphate containing base referred to above is replaced with a base containing zeolite and sodium carbonate but no phosphate.
Using the same spray-dried base powder used in Examples 1 and 2, compositions were prepared having the following formulations (% by weight).
.
~L3~3~
- 17 - C.3044 Example No: Control D E 3 F ~ 4 Base powder65 65 65 65 65 65 65 Clay - l - 10 10 10 Clay - 2 ~ 10 10 10 Cellulase - - - 1.0* - - 1.0*
Alcalase - - 0.21**- - 0~21**-Sodium perborate 21 2121 21 21 21 21 Sodium sulphate ---------- balance to 100% ~
* Cellulase added to give 10 Cx units/l in the wash ** Alcalase added to give 10 gU/ml in the wash Clay No. 1 is a bentonite having a cation exchange capacity of 95 meg/lOOg while Clay No~ 2 is a bentonite having a cation exchange capacity of 31 meg/lOOg Using the same evaluation method as described in connection with Examples 1 and 2 the softness of terry towelling monitors was assessed and the results were as ~ollows:
~5 Example No: Control D E 3 F G 4 % sotness 100 106 104 113 105 103 107 These results demonstrate that in the case of clay No. 1, in comparison with the Control, the presence of clay improves softening lExample D) and this softening is further improved by the additional presence of cellulase (Example 3) but not by the additional presence of alcalase (Example E). The same conclusion can be drawn from the results of those Examples which contain Clay No. 2.
lExamples F, G and 4). It is also apparent from these results that Clay No. 1 shows improved results over Clay No. 2, particularly in the presence of cellula~e (compare Examples 3 and 4 ) .
..
Claims (7)
1. A detergent composition for cleaning and softening fabrics which includes:
(i) from 5 to 50% of a detergent active material;
(ii) from 1.5 to 35% of a fabric softening clay material; and (iii) from 0.1 to 10% of cellulase;
the balance of the composition comprising other detergent ingredients.
(i) from 5 to 50% of a detergent active material;
(ii) from 1.5 to 35% of a fabric softening clay material; and (iii) from 0.1 to 10% of cellulase;
the balance of the composition comprising other detergent ingredients.
2. A composition according to claim 1, wherein the fabric softening clay material is a bentonitic clay.
3. A composition according to claim 1, wherein the cellulase is selected from bacterial and fungal cellulases having a pH
optimum of between 5 and 11.5.
optimum of between 5 and 11.5.
4. A method of cleaning and softening fabrics comprising contacting the fabrics with a wash liquor to which has been added a detergent composition comprising from 5 to 50% of a detergent active material, from 1.5 to 35% of a fabric softening clay material and from 0.1 to 10% of cellulase, the balance of the composition comprising other detergent ingredients.
5. A method of preparing a detergent composition according to claim 1, which method comprises forming an aqueous slurry of at least a detergent active material and a detergency builder material, spray-drying the slurry to form base granules and adding to the granules cellulase and a fabric softening clay material.
6. A method of preparing a detergent composition according to claim 1, which method comprises forming an aqueous slurry of a detergent active and a fabric softening clay material, spray-drying the slurry to form base granules and adding cellulase to the base granules.
7. A composition according to claim 1, 2 or 3 wherein the detergent active material comprises anionic or mixed anionic and nonionic detergent active materials.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB848421802A GB8421802D0 (en) | 1984-08-29 | 1984-08-29 | Detergent composition |
| GB8421802 | 1984-08-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1308374C true CA1308374C (en) | 1992-10-06 |
Family
ID=10565969
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000489502A Expired - Fee Related CA1308374C (en) | 1984-08-29 | 1985-08-27 | Detergent composition |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0177165B1 (en) |
| AT (1) | ATE61399T1 (en) |
| AU (1) | AU561138B2 (en) |
| BR (1) | BR8504091A (en) |
| CA (1) | CA1308374C (en) |
| DE (1) | DE3581996D1 (en) |
| GB (1) | GB8421802D0 (en) |
| ZA (1) | ZA856551B (en) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8627914D0 (en) * | 1986-11-21 | 1986-12-31 | Procter & Gamble | Softening detergent compositions |
| US4822516A (en) * | 1986-12-08 | 1989-04-18 | Kao Corporation | Detergent composition for clothing incorporating a cellulase |
| US4832864A (en) * | 1987-09-15 | 1989-05-23 | Ecolab Inc. | Compositions and methods that introduce variations in color density into cellulosic fabrics, particularly indigo dyed denim |
| GB8727081D0 (en) * | 1987-11-19 | 1987-12-23 | Procter & Gamble | Granular detergent compositions |
| GB8816112D0 (en) * | 1988-07-06 | 1988-08-10 | Unilever Plc | Detergent compositions |
| NZ230842A (en) * | 1988-10-21 | 1992-05-26 | Colgate Palmolive Co | Nonionic heavy duty particulate detergent containing protease, amylase and cellulase |
| DE8901770U1 (en) * | 1989-02-15 | 1990-07-26 | Schaltbau Gmbh, 8000 Muenchen, De | |
| ES2174820T3 (en) * | 1991-01-16 | 2002-11-16 | Procter & Gamble | COMPOSITIONS OF COMPACT DETERGENTS WITH HIGH ACTIVITY CELL. |
| US5443750A (en) * | 1991-01-16 | 1995-08-22 | The Procter & Gamble Company | Detergent compositions with high activity cellulase and softening clays |
| US5668073A (en) * | 1991-11-06 | 1997-09-16 | The Procter & Gamble Company | Detergent compounds with high activity cellulase and quaternary ammonium compounds |
| AU662120B2 (en) * | 1992-02-18 | 1995-08-24 | Procter & Gamble Company, The | Detergent compositions with high activity cellulase and softening clays |
| AU2244992A (en) * | 1992-02-18 | 1993-09-03 | Procter & Gamble Company, The | Detergent compositions with high activity cellulase and quaternary ammonium compounds |
| EP0633311B1 (en) * | 1993-06-28 | 2000-05-17 | The Procter & Gamble Company | Hydrophobic amines for cellulase stabilization in liquid detergent compositions containing anionic surfactant and cellulase |
| US5883066A (en) * | 1993-06-28 | 1999-03-16 | The Procter & Gamble Company | Liquid detergent compositions containing cellulase and amine |
| WO1995027036A1 (en) * | 1994-03-30 | 1995-10-12 | The Procter & Gamble Company | Laundry detergent bars containing fabric softening clay and cellulase enzyme |
| US5558676A (en) * | 1995-03-15 | 1996-09-24 | Ocean Wash, Inc. | Composition and a method for treating garments with the composition |
| US5593458A (en) * | 1995-03-16 | 1997-01-14 | Ocean Wash, Inc. | Process and composition for decorating a dyed cloth fabric |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3936537A (en) * | 1974-11-01 | 1976-02-03 | The Procter & Gamble Company | Detergent-compatible fabric softening and antistatic compositions |
| ATE10646T1 (en) * | 1979-09-29 | 1984-12-15 | The Procter & Gamble Company | DETERGENT COMPOSITIONS. |
| GB2094826B (en) * | 1981-03-05 | 1985-06-12 | Kao Corp | Cellulase enzyme detergent composition |
-
1984
- 1984-08-29 GB GB848421802A patent/GB8421802D0/en active Pending
-
1985
- 1985-08-26 AU AU46645/85A patent/AU561138B2/en not_active Ceased
- 1985-08-27 CA CA000489502A patent/CA1308374C/en not_active Expired - Fee Related
- 1985-08-27 BR BR8504091A patent/BR8504091A/en not_active IP Right Cessation
- 1985-08-27 AT AT85306056T patent/ATE61399T1/en not_active IP Right Cessation
- 1985-08-27 EP EP19850306056 patent/EP0177165B1/en not_active Revoked
- 1985-08-27 DE DE8585306056T patent/DE3581996D1/en not_active Revoked
- 1985-08-28 ZA ZA856551A patent/ZA856551B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0177165B1 (en) | 1991-03-06 |
| BR8504091A (en) | 1986-06-17 |
| GB8421802D0 (en) | 1984-10-03 |
| AU561138B2 (en) | 1987-04-30 |
| DE3581996D1 (en) | 1991-04-11 |
| ZA856551B (en) | 1987-05-27 |
| EP0177165A3 (en) | 1989-05-03 |
| AU4664585A (en) | 1986-03-06 |
| ATE61399T1 (en) | 1991-03-15 |
| EP0177165A2 (en) | 1986-04-09 |
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