CA1191068A - Detergent additives and detergent compositions containing them - Google Patents
Detergent additives and detergent compositions containing themInfo
- Publication number
- CA1191068A CA1191068A CA000407291A CA407291A CA1191068A CA 1191068 A CA1191068 A CA 1191068A CA 000407291 A CA000407291 A CA 000407291A CA 407291 A CA407291 A CA 407291A CA 1191068 A CA1191068 A CA 1191068A
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- Prior art keywords
- weight
- soap
- detergent
- detergent additive
- chain length
- 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.)
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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
- C11D3/02—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
- C11D3/128—Aluminium silicates, e.g. zeolites
-
- 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
- C11D3/20—Organic compounds containing oxygen
- C11D3/2075—Carboxylic acids-salts thereof
-
- 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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/33—Amino carboxylic acids
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
Abstract
ABSTRACT
A ternary builder system for detergent compositions comprises 25 to 97% by weight of an aluminosilicate cation-exchange material such as Zeolite A and 3 to 75% by weight, in total, of (i) a soap containing at least 60% by weight of saturated material, and (ii) nitrilotriacetic acid or a water-soluble salt thereof, at a (i):(ii) ratio of 10:1 to 1:10, the proportion of soap in the ternary mix being at least 12%. The builder mix is advantageously used in detergent compositions containing less than 10% inorganic phosphate, and gives good results in zero-phosphate compositions.
A ternary builder system for detergent compositions comprises 25 to 97% by weight of an aluminosilicate cation-exchange material such as Zeolite A and 3 to 75% by weight, in total, of (i) a soap containing at least 60% by weight of saturated material, and (ii) nitrilotriacetic acid or a water-soluble salt thereof, at a (i):(ii) ratio of 10:1 to 1:10, the proportion of soap in the ternary mix being at least 12%. The builder mix is advantageously used in detergent compositions containing less than 10% inorganic phosphate, and gives good results in zero-phosphate compositions.
Description
-1~9~8 DETERGENT ADDITIVES AND DETERGENT COMPOSITIONS
CO~TAINING THEM
The present invention relates to additives for detergent compositions, and to detergent compositions containing them~ These compositions are particularly, but not essentially~ adapted for fabric washing. The invention relates more particularly to substantially phosphate-free detergent compositions.
Fabric washing compositions conventionally contain phosphate detergency builders such as sodium tripolyphosphate. In some circumstances it is thought that the use of phosphates in detergent compositions can lead to environmental problems in waste waters. There is therefore a desire to reduce the level of phosphorus, or to eliminate it altogether, in detergent compositions.
Water-insoluble aluminosilicate ion exchange materials have been suggested as alternative builders to phosphates;
see, for example, GB l,473,201 and GB l,473,202 (Henkel).
It has been found in practice, however, that these aluminosilicate materials, even in large amounts, tend to P6E21E ~
.~
1~9~
CO~TAINING THEM
The present invention relates to additives for detergent compositions, and to detergent compositions containing them~ These compositions are particularly, but not essentially~ adapted for fabric washing. The invention relates more particularly to substantially phosphate-free detergent compositions.
Fabric washing compositions conventionally contain phosphate detergency builders such as sodium tripolyphosphate. In some circumstances it is thought that the use of phosphates in detergent compositions can lead to environmental problems in waste waters. There is therefore a desire to reduce the level of phosphorus, or to eliminate it altogether, in detergent compositions.
Water-insoluble aluminosilicate ion exchange materials have been suggested as alternative builders to phosphates;
see, for example, GB l,473,201 and GB l,473,202 (Henkel).
It has been found in practice, however, that these aluminosilicate materials, even in large amounts, tend to P6E21E ~
.~
1~9~
- 2 - C.1303/1 be undesirably slow in their exchange of cations, especially at low temperatures, resulting in inferior detergency. It has accordingly been suggested that supplementary water-soluble builders should be used in combination with these aluminosilicates to raise the detergency to an acceptable level. These supplementary builders are generally materials that are efficient sequestrant builders in their own right, for example, alkali metal tripolyphosphates, nitrilotriacetates and poly- C~ -hydroxyacrylates. High levels of these materials are, however, not generally desirable in detergent compositions for cost or environmental reasons.
We have now discovered that surprisingly good detergency results are obtained by using, in combination with an aluminosilicate builder, relatively small amounts of both a specific organic sequestrant builder (nitrilo-triacetic acid or a salt thereof) and a specific organic precipitant builder (a defined soap or soap blend). The 20 detergency results obtained using ternary systems of this type have surprisingly been found to be better than would have been expected from consideration of the results obtained using the corresponding binary aluminosilicate/
sequestrant and aluminosilicate/precipitant systems, so 25 that decreased amounts of the supplementary builders can be used, giving cost savings and environmental advantages.
It is known that the detergency builder properties of aluminosilicates are enhanced by the addition of water-3o soluble complexing agents such as sodium tripolyphosphate.This effect has been explained in terms of the so-called "carrier molecule model": see, for example, P Berth, J. Am. Oil Chemists' Soc., 55 , 52-53 (1978). The complexing agent is able to take up polvalent water hardness ions (notably Ca2+, but also Mg2+) from solid surfaces (such as the surface of a textile fibre) and pass them on to the aluminosilicate ion exchanger after transport through the aqueous medium. The complexing agent forms a chelate complex with the hardness ion which on arrival at the surface of the aluminosilicate dissociates.
It is not easy to envisage a similar mechanism with precipitant builders, such as soaps, since these remove hard-ness ions from the wash liquor by the virtually irre~ersible formation of a precipitate ~insoluhle calcium or magnesium salt).
It is thus unexpected that addition of a soap to an aluminosilicate/sequestrant system gives a substantial im-provement in detergency builder properties.
The present invention accordingly provides, in a first aspect, a detergent additive consisting of:
~a) at least 25% by weight of a crystalline or amorphous aluminosilicate cation-exchange material, (b) the balance consisting of (i) one or more water-soluble soaps of C8-C22 fatty acids, at least 60% by weight of the total soap being sat-urated material, (ii) nitrilotriacetic acid or a water-soluble salt thereof, the weight ratio of (i) to (ii) being from 3:1 to 1:3, and (i) being present in an amount of at least 12% by weight based on the total weight of (a) and (b).
Component (b)(ii) will hereinafter be referred to as NTA.
Thus the subject of the invention is a ternary builder system consisting of aluminosilicate, soap and NTA.
i~9~ o~
- 4 - C.1303/1 In GB 1 498 492 (Henkel) and DE 25 33 110 (Henkel) there are disclosed detergent compositions, built with aluminosilicate and NTA, in which the detergent-active system includes soap; the soap is, however, present only in small quantities.
EP 38 591 (Procter & Gamble) discloses detergent compositions built with aluminosilicate in which the detergent-active agents used include soaps of C16-C22 10 unsaturated fatty acids. These soaps function in the compositions as detergent-active agents, assisting in soil removal and cool-water detergency; the aluminosilicate is said to assist in keeping the unsaturated soap from forming an insoluble curd D The unsaturated soaps are not, 15 accordingly, functioning as builders by precipitating calcium from the wash liquor as an insoluble calcium soap.
The soap compositions disclosed in EP 38 591 may contain some saturated soap, but only at low levels so as not to detract from the detergent activity o the preferred 20 unsaturated materials.
The unsaturated soaps disclosed in EP 38 591 are unsuitable for use in the compositions of the present invention, because their calcium salts are not sufficiently 25 insoluble in water. The predominantly saturated soaps used according to the inventon, on the other hand, have highly insoluble calcium salts. Calcium present in the wash liquor is removed in the form of insoluble calcium soaps;
the soaps themselves thus function as builders rather than 3O as detergent-active agents.
The soaps used in the compositions of the invention consist to an extent of at least 60%, preferably at least 80%, of saturated soaps. Advantageously 100% saturated material may be used.
1191~
- 5 - C.1303/1 The soap preferably contains both longer-chain (C18 and above) and shorter-chain (C14 and below) material.
The longer the chain, the higher the insolubility of the of the calcium salt, and thus the greater the efficiency of the soap as a builder. Shorter chain-length soaps, however, although forming less insoluble calcium salts, can also be effective detergency builders because of their lower molecular weight and accordingly greater weight-effectiveness. The shorter-chain soaps are especially valuable under low temperature washing conditions.
Shorter-chain soaps themselves (generally the sodium salts) also have better solubility then the longer-chain 15 materials, and the presence of some short-chain material along with longer-chain soaps can enhance overall soap solubility.
In general, for efficient building, the soap used in the detergent additive of the invention preferably contains at least 5% by weight, more preferably at least 8%, of material having a chain length of Cl~ and above. It may also be advantageous, from the point of view of solubility, for the soap used in the detergent additive of the invention to contain at least 1~, preferably at least 3~, of material being a chain length of C14 and below.
When predominantly longer-chain soaps are used in the detergent additive of the invention, the soap or mixture of soaps contains at least 60% by weight, preferably at least 80% by weight, of material having a chain length of C18 and above. It is also advantageous, from the point of view of solubility, for the soap to contain at least 1~, preferably at least 3%, of material having a chain length of C14 and below. This is not essential, however, for products intended for use in conventional medium or - 6 - C.1303/l high-temperature washing, where the solubility of the soap itself (the sodium or other soluble salt) is not a problem.
Examples of such soaps include hardened tallow (67% C18 and above) and hardened rapeseed (96.5% Cl8 and above).
When predominantly shorter-chain soaps are used in the detergent additive of the invention, the soap or mixture of 10 soaps contains at least 60% by weight, preferably at least 7C~ by weight, of material having a chain length of C14 and below. It preferably also contains at least 5%, more preferably at least 8%, of material having a chain lengh of Cl8 and above. Such a composition is especially 15 beneficial for lower-temperature washing where the solubility of the soap itself is important in determining good detergency building.
Examples of such soaps include coconut (82% Cl4 and 20 below) and palm kernel (73.5% C14 and below).
The following Table shows the constitution of the four soaps mentioned above:
L06~
- 7 - C.1303/1 _._________________________________________________________ Soap ¦ Hardened ¦ Hardened ¦ Coconut ¦ Palm tallow ¦ rapeseed ¦ ¦ kernel _________________I__ _______I__________I_________I__ _____ Saturated material (%) ¦ 100 ¦ 100 ¦ 92.5 ¦ 85.5 _________________I~_________I_______~__I_________I________ 5 Chain length distribution (%) ¦ l l l C10 and below ¦ _ ¦ _ ¦13.0 ¦ 7.5 C12 1 _ I _ 149.5 148.5 C14 13,5 1 - ~19.5 117.5 C15 ¦0 5 ¦ ~ ¦ ~ ¦ ~
C16 127.5 1 3.5 18.5 110.5 C17 11.5 1 _ I _ I _ C18 166.5 137.2 19.5 116.0 c2o 10,5 1 6.6 C22 ¦ _ ¦52.7 _________________________________________________________ These are of course only exemplary of the many soaps and soap blends that may be used in the detergent additive of the invention.
The detergent additive of the invention also includes 20 a water-insoluble aluminosilicate cation exchange material~
This is a crystalline or amorphous material having the general formula:
(Cat2/n o)X-A12o3(sio23Y 2 wherein Cat is a cation having valency n that is 25 exchangeable with calcium (e.g. Na+ or K+); x is a number from 0.7-1.5; y is a number from 1.3-~; and z is 6~
- 8 - C.1303/1 such that the bound water content is from 10% to 23% by weight.
Pr~ferably a crystalline material is used which can be described by the unit ceIl content:
Nax ~A1O2)X-(siO2)~ Z~2 wherein x and y are integers of at least 6, the ratio of x to y being in the range o 1:1 to 1:2; and z is such that the bound water content is from 10~ to 28% by weight.
The aluminosilicate preferably has a particle size of from 0.1 to 100 micrometres, ideally between 0.1 and 10 micrometres, and an ion exchange capacity of at least 200 mg CaCO3 per gram of aluminosilicate (anhydrous basis~.
In a preferred embodiment the water-insoluble aluminosilicate is a crystalline material having the formula described by the unit cell content:
Nal2LAlo2)12 (sio2)12]~ 2 wherein z is from 20 to 30, preferably about 27.
An example of this material is the commercially available product ~nown as Zeolite type A, which is typically:
Na2o.Al2o3 2sio2 4 5H20 and is also described by the unit cell content:
al2 ~A1O2)l2~(sio2)l2].27H2o.
The third component of the detergent additive of the invention is an organic sequestrant builder, namely, nitrilotriacetic acid or a water-soluble salt thereof ~L~9~6~3 - 9 - C.1303/1 (NTA). This component may be represented by the following structural formula _( 2.COOX)3 wherein X is hydrogen or a solubilizing cation. These compounds may further contain C bonded substituents of an inert and innoxious nature such as alkyl, eg methyl or ethyl, or haloalkyl, eg chloromethyl. The nature of said compounds is ~ot particularly critical with the implicit limitation that such substituents be devoid of any tendency to deleteriously affect the desirable properties of the NTA.
Preerred compounds falling within the ambit of the above-described definition and formula are nitrilotriacetic acid and its alkali metal salts, especially trisodium nitrilotriacetate monohydrate, tripotassium nitrilotriacetate 9 disodium nitrilotriacetate and dipotassium nitrilotriacetate.
The soap and NTA together constitute from about 3% to about 75% by weight of the builder mix (detergent additive) of the invention, preferably from about 10% to about 60%
and especially from about 20% to about 50%. The ratio of soap to NTA is from 10:1 to 1:10, preferably from 3:1 to 1:3 and desirably from 3:1 to 1:1.
The detergent additive of the present invention is an efficient builder system yielding good detergency results when incorporated, with detergent-active materials, in a detergent composition.
Accordingly, in a second aspect the present invention provides a detergent composition comprising from about 3 to - 10 - C.1303/1 about 90% by weight of at least one synthetic detergent-active material, and from about 10 to about 97%
by weight of a detergent additive as previously defined.
The detergent composition of the invention contains from about 10% to about 97% by weight of the detergent additive of the invention, preferably from about 10% to about 80%. more preferably from about 25~ to about 70%, and especially from abou~ 28% to about 67%.
Since the detergent additive contains from about 25%
to about 97% by weight of aluminosilicate, the aluminosilicate content of the detergent composition can range from about 2.5% to about 94%. An aluminosilicate content of from about 10~ to about 60%, especially from about 17% to about 47%, is preferred.
Similarly, the content of the specified organic builders (soap plus ~TA) can range from about 0.3% to about 73%, a range of from about 5% to about 40%, especially from about 7% to about 27%, being preferred~ The preferred range for the content of the soap is from about 3% to about 20%, especially from about 5% to about 10%; for the NTA
the preferred range is from about 1% to about 15%, especially from about 2% to about 10~.
The detergent compositions of the present invention are preferably substantially free of inorganic phosphate.
This is highly desirable for the environmental reasons mentioned earlier. Compositions according to the invention containing no inorganic phosphate have been found to exhibit detergency properties comparable to those of sodium tripolyphosphate-built products.
If desired, however, the compositions may contain inorganic phosphate, but if avoidance of the possible gl~6~
- 11 - C.1303/1 environmental effects of phosphate is in ~uestion the level advantageously does not exceed 10% based on the whole product; levels below 5% and more especially below 3% are of particular interest in this connexion. Any phosphate present may, for example, be in the form o~ alkali metal (preferably sodium) tripolyphosphate, orthophosphate, pyrophosphate or polymeric phosphate.
The detergent composition of the invention may if desired contain other builders in addition to the specified ternary builder system of the invention. As indicated previously, these are preferably non-phosphate materials.
Examples of suitable materials include the water-soluble salts of the following acids: ethylenediamine tetracetic acid, polyacrylic acid, poly(CX-hydroxyacrylic) acid, carboxymethyloxymalonic acid, carboxymethyloxysuccinic acid, oxydiacetic acid, oxydisuccinic acid, citric acid, dipicolinic acid and many more. The polyacetal carboxylates disclosed in US 4,144,126 and US 4,146,495 (Monsanto) and the oxidised polysaccharides disclosed in GB
1,330,121, GB 1,330,122 and ~B 1,330,123 (Unilever) may also advantageously be used.
The detergent composition of the invention necessarily includes from about 3% to about 90% by weight, preferably from about 5% to about 40% by weight, more preferably from about 10% to about 25% by weight, of a synthetic anionic, nonionic, amphoteric or zwitterionic detergent compound or mixture thereof. Many suitable detergent-active compounds are commercially available and are fully described in the literature, for example in "Surface ~ctive Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
The preferred detergent compounds which can be used ~19~ 6~
- 12 - C.1303~1 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 aryl radicals.
Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C8-C18~ alcohols produced for example from tallow or coconut oil; sodium and potassium alkyl (Cg-C20) benzene sulphonates, particularly sodium linear secondary alkyl (C10-Cl5) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty acid monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (Cg-Cl8) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralis~d 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 bisulphate and those derived by 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-Examples of suitable nonionic detergent compoundswhich may be used include in particular the reaction ~5 products of alkylene oxides, usually ethylene oxide, with alkyl (C6-C22) phenols, generally 5 to 25 E0, ie 5 to - 13 - C.1303/1 25 units of ethylene oxide per molecule; the condensation products of aliphatic (~8-Cl8) primary or secondary linear or branched alcohols with ethylene oxide, generally 6 to 30 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Other so-called nonionic detergent compounds include long chain tertiary amine oxides, 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. Anionic and nonionic detergent compounds are advantageously used together in ratios of from 3:1 to 1.5:1.
Amounts of amphoteric or zwitterionic detergent compounds can also be used in the compositions of the invention but this is 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.
According ~o a preferred embodiment of the invention, the detergent composition also contains a bleach system.
The b~each system preferably comprises a peroxy bleach compound which is an inorganic persalt, which is preferably used in conjunction with an activa~or therefor. The persalt may be, for example, sodium perborate (either the monohydrate or the tetrahydrate) or sodium percarbonate.
The activator makes the bleaching more effective at lower temperatures, ie in the range from ambient temperature to ~191(~
- 14 - C.1303/l about 60C, so that such bleach systems are commonly known as low-temperature bleach systems and are well known in the art. The inorganic persalt acts to release active oxygen in solution, and the activator is usually an organic compound having one or more reactive acyl residues, which cause the formation of peracids, the latter providin~ for a more e~fective bleaching action at lower temperatures than can be obtained by use of the peroxy bleach compound alone.
The ratio by weight of the peroxy bleach compound to the activator is generally from about 20:1 to about l:l, preferably about 15:1 to about 2:1.
The detergent composition of the invention preferably contains from about 5% to about 30% by weight of the peroxy bleach compound, and about 0.1 to about 15% by weight of the activator. The total amount of the bleach system ingredients preferably lies within the range of from 5% to 35% by weight, especially from about 6~ to about 30% by weight.
Typical examples of suitable peroxy bleach compounds are alkali metal perborates, both tetrahydrates and monohydrates, alkali metal percarbonates, persilicates and perphosphates, of which sodium perborate is preferred.
Activators for peroxybleach compounds have been amply described in the literature, including British patents 836,988, 855,735, 907,356, 907,358, 970,950, 1,003,310 and 1,246,339, US patents 3,332,882 and 4,128,494, Canadian patent 844,481 and South African patent 68/6,344. Speci~ic suitable activators include:
(a) N-diacylated and N,N'-polyacylated amines, such as N,N,N',N'-tetraacetyl methylene diamine and N,N,N',N'-tetraacetyl ethylene diamine, N,N-diacetylaniline, N,N-diacetyl-p~toluidine;
~191V6~3 - 15 - C.1303/1 1,3-diacylated hydantoins such as, for example, 1,3-diacetyl-5,5-dimethyl hydantoin and 1,3-dipropionyl hydantoin; D~-acetoxy-(N,N')-polyacylmalonamide, for example D<-acetoxy-(N,N')-diacetylmalonamide;
(b) N-alkyl-N-sulphonyl carbonamides, for example the compounds N-methyl-N-mesyl--acetamide, N-methyl-N-mesyl-benæamide, N-methyl-N-mesyl-p-nitrobenzamide, and N-methyl-N-mesyl-p-methoxybenzamide;
(c) N-acylated cyclic hydrazides, acylated triazones or uraæoles, for example monoacetylmaleic acid hydrazide;
(d~ 0,N,N-trisubstituted hydroxylamines, such as 0-benzoyl-N,N-succinyl hydroxylamine, 0-acetyl-N,N-succinyl hydroxylamine, ~5 0-p-methoxybenzoyl N,N-succinyl-hydroxylamine, 0-p-nitrobenzoyl-N r N-succinyl-hydroxylamine and 0,N,N-triacetyl hydroxylamine;
(e) N,N'-diacyl-sulphurylamides, for example N,N'-dimethyl-N,N'-diacetyl-sulphurylamide and N,N'-diethyl-N,N'-dipropionyl sulphurylamidei (f) Triacylcyanurates, for example triacetyl cyanurate and tribenzoyl cyanurate;
(g) Carboxylic acid anhydrides, such as benzoic anhydride, m-chloro-benzoic anhydride, phthalic anhydride, 4-chloro-phthalic anhydride;
(h) Sugar esters, for example glucose pentaacetate;
(i) 1,3-diacyl-4,5-diacyloxy-imidazolidine, for example 1,3-diformyl-4,5-diacetoxy-imidazolidine, 1,3-diacetyl-4,5-diacetoxy-imidazolidine, 1,3-diacetyl-4,5-dipropionyloxy-imidazoline;
(j) Tetraacetylglycoluril and tetrapropionylglycoluril;
(k) Diacylated 2,5-diketopiperazine, such as 1,4-diacetyl-2,5-diketopiperazine, 1,4~dipropionyl 2,5-diketopiperazine and 1,4-dipropionyl-3,6-dimetyl-~5 2,5-diketopiperazine;
(1) Acylation products o~ propylenediurea or 2r2-dimethyl-~19~
- 16 - C.1303/1 propylenediurea (2,4,6,8-tetraaza-bicyclo-(3,3,1)-nonane-3,7-dione or its 9,9-dimethyl derivative), especially the tetraacetyl- or the tetrapropionyl-propylenediurea or their dimethyl derivatives;
(m) Carbonic acid esters, for example the sodium salts of p-(ethoxycarbonyloxy)-benzoic acid and p-(propoxy-carbonyloxy)-benzenesulphonic acid.
(n) ~-acyloxy-(N,N') polyacyl malonamides, such as D<-acetoxy-tN~N~) diacetyl malonamide.
The N~diacylated and ~,N'-polyacylatedamines mentioned under (a) are of special interest, particularly N,N,N',N'-tetra-acetyl-ethylenediamine (TAED).
It is preferred to use the activator in granular form, preferably wherein the activator is finely divided as described in our UK Patent Application No. 80 21979.
Specifically, it is preferred to have an activator of an average particle size of less than 150 micrometres, which gives significant improvement in bleach efficiency. The sedimentation losses, when using an activator with an average particle size of less than 150 /um, are substantially deGreased. Even better bleach performance is obtained if the average particle size of the activator is less than 100 /um. However, too small a particle size gives increased decomposition, dust-formation and handling problems, and although particle sizes below 100 /um can provide for an improved bleaching efficienc~, it is desirable that the activator should not have more than 20%
by weight of particles with a size of less than 50 /um.
On the other hand, the activator may have a certain amount of particles of a si~e greater than 150 /um, but it should not contain more than 5% by weight of particles ~' 300 /um, and not more than 20% by weight of particles > 200 /um, preferably > 150 /um. It is to be understood that these particle sizes refer to the activator ~91~
- 17 - ~.1303/1 present in the granules, and not to the granules themselves. The latter have a particle size, the major part of it ranging from 100 to 2000 /um, preferably 250 to 1000 /um. Up to 5% by weight of granules with a particle size of ~ 1700 /um and up to 10% by weight of granules ~ 250 /um is tolerable. The granules incorporating the activator, preferably in this finel~-divided form, may be obtained by granulating a suitable carrier material, such as sodium tripolyphosphate and/or potassium tripolyphosphate with activator particles of the required size. Other granulation methods, e.g. using organic and/or inorganic granulation aids, can also be usefully applied. The granules can be subsequently dried, if required.
Basically, any granulation process is appli~able, as long as the granule contains the activator, and as long as the other materials present in the granule do not negatively affect the activator.
It is particularly preferred to include in the detergent compositions a stabiliser for the bleach system, for example ethylene diamine tetramethylene phosphonate and diethylene triamine pentamethylene phosphonate. These stabilisers can be used in acid or salt form, especially in calcium, magnesium, zinc or aluminium salt form, as described in our UK Patent Application No. 2 048 930.
Apart from the components already mentioned, the detergent compositions of the invention can contain any of the conventional additives in the amounts in which such materials are normally employed in fabric washing detergent compositions. Examples of these additives include lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids; lather depressants such as al~yl - 1~91C~
~ C.1303/1 phosphates, silicones, or alkyl phosphonic acids incorporated in petroleum jelly, wax or mineral oil;
anti-redeposition agents such as sodium carboxymethyl-cellulose and cellulose ethers; fabric softening agents;
inor~anic salts such as sodium sulphate and sodium carbonate; and, usually present in very minor amounts, fluorescent agents, perfumes, enzymes such as proteases and amylases.
It may be desirable to include in the composition an amount of an alkali metal silicate, particularly sodium ortho-, meta- or pre~erably neutral or alkaline silicateO
The presence of such alkali metal silicates at levels of at least ~bout 1%, and preferably from about 5~ to about 15%
by weight of the composition, is advantageous in decreasing the corrosion of metal parts in washing machines, besides giving processing benefits and generally improved powder properties. The more highly alkaline ortho- and meta-silicates would normally only be used at lower amounts within this range, in admixture with the neutral or alkaline silicates.
The composition of the invention is preferably alkaline, but not too strongly alkaline as this could result in fabric damage and also be hazardous for domestic usage. In practice the composition should desirably give a pH of from about 8.5 to about 11 in use in aqueous wash solution. It is preferred in particular for domestic products to have a pH of from about 9.0 to about 10.5 as lower pH's tend to be less effective for optimum detergency building, and more highly alkaline products can be hazardous if misused. The pH is measured at the lowest normal usage concentration of 0.1% w/v of the product in water of 12H (Ca), (French permanen~ hardness, calcium only) at 50C so that a satisfactory degree of alkalinity can be assured in use at all normal product concentrations.
119~0~
- 19 - C.13~3/1 If necessary, up to 10% by weight of alkali metal carbonate, preferably sodium carbonate, may be included in order to raise the pH and to maintain adequate buffer capacity in the presence of acidic soils.
If carbonate or phosphates are present it may be desirable to include in the composition of the invention one or more antideposition agents, to decrease any tendency to form inorganic deposits on washed fabrics. The amount of any such antideposition agent is normally from about 0.1~ to about 5% by weight, preferably from about 0.2% to about 1.5~ by weight of the composition. The preferred antideposition agents are anionic polyelectrolytes, esp~cially polymeric aliphatic carboxylates, or orqanic phosphonates.
The detergent compositions of the invention should desirably be in free-flowing particulate, for example, powdered or granular form, and can be produced by any of the techniques commonly employed in the manufacture of such washing compositions, for example, by slurry-making and spray-drying processes. It is preferred that the process used to form the compositions should result in a product having a moisture content of not more than about 12%, more preferably from about 4% to about 10% by weight.
The detergent compositions of the invention may also be in the form of bars or tablets, or in liquid form.
The invention will now be illustrated by the following non-limiting Examples.
EXAMPLES
In the Examples that follow, the detergencies of wash liquors incorporating various builder systems were compared ~L191(~
- 20 - C.1303/1 by measuring the reflectance of a clay-soiled polyester/cotton test cloth before and after washing in the Tergotometer. The reflectances were measured using a Carl Zeiss Elrepho Reflectometer and the reflectance increase on washing (~R) was taken as a measure of detergency.
In each case a wash liquor was prepared using the ingredients stated below in the concentrations stated below, in 40FH (Ca)water. The wash liquor was allowed to equilibrate for 15 minutes. Test cloth pieces ~four,pieces per litre, each measuring 76.2 mm x 76.2 mm) were then added and a 20-minute wash at 80C, pH
10.0 and 55 rpm agitation was carried out, followed by a rinse in water of the same hardness as that of the water used to prepare the wash liquor.
The ingredients and concentrations were as follows:
g/litre Sodium C10-Cl3 linear alkylbenzene 0.135 sulphonate C14-C15 alcohol ethoxylate (11 EO) 0.09 Hardened tallow soap* 0.06 Alkaline silicate 0.15 Sodium sulphate 2.00 Detergent additive according to the invention (as specified in E~amples) 2.00-5.00 * The soap was included for lather control purposes and was present in addition to the soap included in the detergent additive according to the invention.
~ 21 C~1303/1 It will be seen that the detergent additive according to the invention was used at concentrations of from 2.00 to 5.00 g/litre, and the other components of the composition were used at a constant total concentration of ~.495 g/litre, so that the total concentration ranged from 4.495 to 7.495 g/litre. Thus the percentage of the total composition constituted by the detergent additive of the invention at each concentration of the latter was as follows:
10 ¦ Concentration I .
~ % detergent additive ¦ (of detergent ¦ (total) ¦ in composition additive 1 2~00 1 4.495 1 44.49 ¦ ~.50 ¦ 4.995 ¦ 50O05
We have now discovered that surprisingly good detergency results are obtained by using, in combination with an aluminosilicate builder, relatively small amounts of both a specific organic sequestrant builder (nitrilo-triacetic acid or a salt thereof) and a specific organic precipitant builder (a defined soap or soap blend). The 20 detergency results obtained using ternary systems of this type have surprisingly been found to be better than would have been expected from consideration of the results obtained using the corresponding binary aluminosilicate/
sequestrant and aluminosilicate/precipitant systems, so 25 that decreased amounts of the supplementary builders can be used, giving cost savings and environmental advantages.
It is known that the detergency builder properties of aluminosilicates are enhanced by the addition of water-3o soluble complexing agents such as sodium tripolyphosphate.This effect has been explained in terms of the so-called "carrier molecule model": see, for example, P Berth, J. Am. Oil Chemists' Soc., 55 , 52-53 (1978). The complexing agent is able to take up polvalent water hardness ions (notably Ca2+, but also Mg2+) from solid surfaces (such as the surface of a textile fibre) and pass them on to the aluminosilicate ion exchanger after transport through the aqueous medium. The complexing agent forms a chelate complex with the hardness ion which on arrival at the surface of the aluminosilicate dissociates.
It is not easy to envisage a similar mechanism with precipitant builders, such as soaps, since these remove hard-ness ions from the wash liquor by the virtually irre~ersible formation of a precipitate ~insoluhle calcium or magnesium salt).
It is thus unexpected that addition of a soap to an aluminosilicate/sequestrant system gives a substantial im-provement in detergency builder properties.
The present invention accordingly provides, in a first aspect, a detergent additive consisting of:
~a) at least 25% by weight of a crystalline or amorphous aluminosilicate cation-exchange material, (b) the balance consisting of (i) one or more water-soluble soaps of C8-C22 fatty acids, at least 60% by weight of the total soap being sat-urated material, (ii) nitrilotriacetic acid or a water-soluble salt thereof, the weight ratio of (i) to (ii) being from 3:1 to 1:3, and (i) being present in an amount of at least 12% by weight based on the total weight of (a) and (b).
Component (b)(ii) will hereinafter be referred to as NTA.
Thus the subject of the invention is a ternary builder system consisting of aluminosilicate, soap and NTA.
i~9~ o~
- 4 - C.1303/1 In GB 1 498 492 (Henkel) and DE 25 33 110 (Henkel) there are disclosed detergent compositions, built with aluminosilicate and NTA, in which the detergent-active system includes soap; the soap is, however, present only in small quantities.
EP 38 591 (Procter & Gamble) discloses detergent compositions built with aluminosilicate in which the detergent-active agents used include soaps of C16-C22 10 unsaturated fatty acids. These soaps function in the compositions as detergent-active agents, assisting in soil removal and cool-water detergency; the aluminosilicate is said to assist in keeping the unsaturated soap from forming an insoluble curd D The unsaturated soaps are not, 15 accordingly, functioning as builders by precipitating calcium from the wash liquor as an insoluble calcium soap.
The soap compositions disclosed in EP 38 591 may contain some saturated soap, but only at low levels so as not to detract from the detergent activity o the preferred 20 unsaturated materials.
The unsaturated soaps disclosed in EP 38 591 are unsuitable for use in the compositions of the present invention, because their calcium salts are not sufficiently 25 insoluble in water. The predominantly saturated soaps used according to the inventon, on the other hand, have highly insoluble calcium salts. Calcium present in the wash liquor is removed in the form of insoluble calcium soaps;
the soaps themselves thus function as builders rather than 3O as detergent-active agents.
The soaps used in the compositions of the invention consist to an extent of at least 60%, preferably at least 80%, of saturated soaps. Advantageously 100% saturated material may be used.
1191~
- 5 - C.1303/1 The soap preferably contains both longer-chain (C18 and above) and shorter-chain (C14 and below) material.
The longer the chain, the higher the insolubility of the of the calcium salt, and thus the greater the efficiency of the soap as a builder. Shorter chain-length soaps, however, although forming less insoluble calcium salts, can also be effective detergency builders because of their lower molecular weight and accordingly greater weight-effectiveness. The shorter-chain soaps are especially valuable under low temperature washing conditions.
Shorter-chain soaps themselves (generally the sodium salts) also have better solubility then the longer-chain 15 materials, and the presence of some short-chain material along with longer-chain soaps can enhance overall soap solubility.
In general, for efficient building, the soap used in the detergent additive of the invention preferably contains at least 5% by weight, more preferably at least 8%, of material having a chain length of Cl~ and above. It may also be advantageous, from the point of view of solubility, for the soap used in the detergent additive of the invention to contain at least 1~, preferably at least 3~, of material being a chain length of C14 and below.
When predominantly longer-chain soaps are used in the detergent additive of the invention, the soap or mixture of soaps contains at least 60% by weight, preferably at least 80% by weight, of material having a chain length of C18 and above. It is also advantageous, from the point of view of solubility, for the soap to contain at least 1~, preferably at least 3%, of material having a chain length of C14 and below. This is not essential, however, for products intended for use in conventional medium or - 6 - C.1303/l high-temperature washing, where the solubility of the soap itself (the sodium or other soluble salt) is not a problem.
Examples of such soaps include hardened tallow (67% C18 and above) and hardened rapeseed (96.5% Cl8 and above).
When predominantly shorter-chain soaps are used in the detergent additive of the invention, the soap or mixture of 10 soaps contains at least 60% by weight, preferably at least 7C~ by weight, of material having a chain length of C14 and below. It preferably also contains at least 5%, more preferably at least 8%, of material having a chain lengh of Cl8 and above. Such a composition is especially 15 beneficial for lower-temperature washing where the solubility of the soap itself is important in determining good detergency building.
Examples of such soaps include coconut (82% Cl4 and 20 below) and palm kernel (73.5% C14 and below).
The following Table shows the constitution of the four soaps mentioned above:
L06~
- 7 - C.1303/1 _._________________________________________________________ Soap ¦ Hardened ¦ Hardened ¦ Coconut ¦ Palm tallow ¦ rapeseed ¦ ¦ kernel _________________I__ _______I__________I_________I__ _____ Saturated material (%) ¦ 100 ¦ 100 ¦ 92.5 ¦ 85.5 _________________I~_________I_______~__I_________I________ 5 Chain length distribution (%) ¦ l l l C10 and below ¦ _ ¦ _ ¦13.0 ¦ 7.5 C12 1 _ I _ 149.5 148.5 C14 13,5 1 - ~19.5 117.5 C15 ¦0 5 ¦ ~ ¦ ~ ¦ ~
C16 127.5 1 3.5 18.5 110.5 C17 11.5 1 _ I _ I _ C18 166.5 137.2 19.5 116.0 c2o 10,5 1 6.6 C22 ¦ _ ¦52.7 _________________________________________________________ These are of course only exemplary of the many soaps and soap blends that may be used in the detergent additive of the invention.
The detergent additive of the invention also includes 20 a water-insoluble aluminosilicate cation exchange material~
This is a crystalline or amorphous material having the general formula:
(Cat2/n o)X-A12o3(sio23Y 2 wherein Cat is a cation having valency n that is 25 exchangeable with calcium (e.g. Na+ or K+); x is a number from 0.7-1.5; y is a number from 1.3-~; and z is 6~
- 8 - C.1303/1 such that the bound water content is from 10% to 23% by weight.
Pr~ferably a crystalline material is used which can be described by the unit ceIl content:
Nax ~A1O2)X-(siO2)~ Z~2 wherein x and y are integers of at least 6, the ratio of x to y being in the range o 1:1 to 1:2; and z is such that the bound water content is from 10~ to 28% by weight.
The aluminosilicate preferably has a particle size of from 0.1 to 100 micrometres, ideally between 0.1 and 10 micrometres, and an ion exchange capacity of at least 200 mg CaCO3 per gram of aluminosilicate (anhydrous basis~.
In a preferred embodiment the water-insoluble aluminosilicate is a crystalline material having the formula described by the unit cell content:
Nal2LAlo2)12 (sio2)12]~ 2 wherein z is from 20 to 30, preferably about 27.
An example of this material is the commercially available product ~nown as Zeolite type A, which is typically:
Na2o.Al2o3 2sio2 4 5H20 and is also described by the unit cell content:
al2 ~A1O2)l2~(sio2)l2].27H2o.
The third component of the detergent additive of the invention is an organic sequestrant builder, namely, nitrilotriacetic acid or a water-soluble salt thereof ~L~9~6~3 - 9 - C.1303/1 (NTA). This component may be represented by the following structural formula _( 2.COOX)3 wherein X is hydrogen or a solubilizing cation. These compounds may further contain C bonded substituents of an inert and innoxious nature such as alkyl, eg methyl or ethyl, or haloalkyl, eg chloromethyl. The nature of said compounds is ~ot particularly critical with the implicit limitation that such substituents be devoid of any tendency to deleteriously affect the desirable properties of the NTA.
Preerred compounds falling within the ambit of the above-described definition and formula are nitrilotriacetic acid and its alkali metal salts, especially trisodium nitrilotriacetate monohydrate, tripotassium nitrilotriacetate 9 disodium nitrilotriacetate and dipotassium nitrilotriacetate.
The soap and NTA together constitute from about 3% to about 75% by weight of the builder mix (detergent additive) of the invention, preferably from about 10% to about 60%
and especially from about 20% to about 50%. The ratio of soap to NTA is from 10:1 to 1:10, preferably from 3:1 to 1:3 and desirably from 3:1 to 1:1.
The detergent additive of the present invention is an efficient builder system yielding good detergency results when incorporated, with detergent-active materials, in a detergent composition.
Accordingly, in a second aspect the present invention provides a detergent composition comprising from about 3 to - 10 - C.1303/1 about 90% by weight of at least one synthetic detergent-active material, and from about 10 to about 97%
by weight of a detergent additive as previously defined.
The detergent composition of the invention contains from about 10% to about 97% by weight of the detergent additive of the invention, preferably from about 10% to about 80%. more preferably from about 25~ to about 70%, and especially from abou~ 28% to about 67%.
Since the detergent additive contains from about 25%
to about 97% by weight of aluminosilicate, the aluminosilicate content of the detergent composition can range from about 2.5% to about 94%. An aluminosilicate content of from about 10~ to about 60%, especially from about 17% to about 47%, is preferred.
Similarly, the content of the specified organic builders (soap plus ~TA) can range from about 0.3% to about 73%, a range of from about 5% to about 40%, especially from about 7% to about 27%, being preferred~ The preferred range for the content of the soap is from about 3% to about 20%, especially from about 5% to about 10%; for the NTA
the preferred range is from about 1% to about 15%, especially from about 2% to about 10~.
The detergent compositions of the present invention are preferably substantially free of inorganic phosphate.
This is highly desirable for the environmental reasons mentioned earlier. Compositions according to the invention containing no inorganic phosphate have been found to exhibit detergency properties comparable to those of sodium tripolyphosphate-built products.
If desired, however, the compositions may contain inorganic phosphate, but if avoidance of the possible gl~6~
- 11 - C.1303/1 environmental effects of phosphate is in ~uestion the level advantageously does not exceed 10% based on the whole product; levels below 5% and more especially below 3% are of particular interest in this connexion. Any phosphate present may, for example, be in the form o~ alkali metal (preferably sodium) tripolyphosphate, orthophosphate, pyrophosphate or polymeric phosphate.
The detergent composition of the invention may if desired contain other builders in addition to the specified ternary builder system of the invention. As indicated previously, these are preferably non-phosphate materials.
Examples of suitable materials include the water-soluble salts of the following acids: ethylenediamine tetracetic acid, polyacrylic acid, poly(CX-hydroxyacrylic) acid, carboxymethyloxymalonic acid, carboxymethyloxysuccinic acid, oxydiacetic acid, oxydisuccinic acid, citric acid, dipicolinic acid and many more. The polyacetal carboxylates disclosed in US 4,144,126 and US 4,146,495 (Monsanto) and the oxidised polysaccharides disclosed in GB
1,330,121, GB 1,330,122 and ~B 1,330,123 (Unilever) may also advantageously be used.
The detergent composition of the invention necessarily includes from about 3% to about 90% by weight, preferably from about 5% to about 40% by weight, more preferably from about 10% to about 25% by weight, of a synthetic anionic, nonionic, amphoteric or zwitterionic detergent compound or mixture thereof. Many suitable detergent-active compounds are commercially available and are fully described in the literature, for example in "Surface ~ctive Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
The preferred detergent compounds which can be used ~19~ 6~
- 12 - C.1303~1 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 aryl radicals.
Examples of suitable synthetic anionic detergent compounds are sodium and potassium alkyl sulphates, especially those obtained by sulphating higher (C8-C18~ alcohols produced for example from tallow or coconut oil; sodium and potassium alkyl (Cg-C20) benzene sulphonates, particularly sodium linear secondary alkyl (C10-Cl5) benzene sulphonates; sodium alkyl glyceryl ether sulphates, especially those ethers of the higher alcohols derived from tallow or coconut oil and synthetic alcohols derived from petroleum; sodium coconut oil fatty acid monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (Cg-Cl8) fatty alcohol-alkylene oxide, particularly ethylene oxide, reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralis~d 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 bisulphate and those derived by 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-Examples of suitable nonionic detergent compoundswhich may be used include in particular the reaction ~5 products of alkylene oxides, usually ethylene oxide, with alkyl (C6-C22) phenols, generally 5 to 25 E0, ie 5 to - 13 - C.1303/1 25 units of ethylene oxide per molecule; the condensation products of aliphatic (~8-Cl8) primary or secondary linear or branched alcohols with ethylene oxide, generally 6 to 30 EO, and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine. Other so-called nonionic detergent compounds include long chain tertiary amine oxides, 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. Anionic and nonionic detergent compounds are advantageously used together in ratios of from 3:1 to 1.5:1.
Amounts of amphoteric or zwitterionic detergent compounds can also be used in the compositions of the invention but this is 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.
According ~o a preferred embodiment of the invention, the detergent composition also contains a bleach system.
The b~each system preferably comprises a peroxy bleach compound which is an inorganic persalt, which is preferably used in conjunction with an activa~or therefor. The persalt may be, for example, sodium perborate (either the monohydrate or the tetrahydrate) or sodium percarbonate.
The activator makes the bleaching more effective at lower temperatures, ie in the range from ambient temperature to ~191(~
- 14 - C.1303/l about 60C, so that such bleach systems are commonly known as low-temperature bleach systems and are well known in the art. The inorganic persalt acts to release active oxygen in solution, and the activator is usually an organic compound having one or more reactive acyl residues, which cause the formation of peracids, the latter providin~ for a more e~fective bleaching action at lower temperatures than can be obtained by use of the peroxy bleach compound alone.
The ratio by weight of the peroxy bleach compound to the activator is generally from about 20:1 to about l:l, preferably about 15:1 to about 2:1.
The detergent composition of the invention preferably contains from about 5% to about 30% by weight of the peroxy bleach compound, and about 0.1 to about 15% by weight of the activator. The total amount of the bleach system ingredients preferably lies within the range of from 5% to 35% by weight, especially from about 6~ to about 30% by weight.
Typical examples of suitable peroxy bleach compounds are alkali metal perborates, both tetrahydrates and monohydrates, alkali metal percarbonates, persilicates and perphosphates, of which sodium perborate is preferred.
Activators for peroxybleach compounds have been amply described in the literature, including British patents 836,988, 855,735, 907,356, 907,358, 970,950, 1,003,310 and 1,246,339, US patents 3,332,882 and 4,128,494, Canadian patent 844,481 and South African patent 68/6,344. Speci~ic suitable activators include:
(a) N-diacylated and N,N'-polyacylated amines, such as N,N,N',N'-tetraacetyl methylene diamine and N,N,N',N'-tetraacetyl ethylene diamine, N,N-diacetylaniline, N,N-diacetyl-p~toluidine;
~191V6~3 - 15 - C.1303/1 1,3-diacylated hydantoins such as, for example, 1,3-diacetyl-5,5-dimethyl hydantoin and 1,3-dipropionyl hydantoin; D~-acetoxy-(N,N')-polyacylmalonamide, for example D<-acetoxy-(N,N')-diacetylmalonamide;
(b) N-alkyl-N-sulphonyl carbonamides, for example the compounds N-methyl-N-mesyl--acetamide, N-methyl-N-mesyl-benæamide, N-methyl-N-mesyl-p-nitrobenzamide, and N-methyl-N-mesyl-p-methoxybenzamide;
(c) N-acylated cyclic hydrazides, acylated triazones or uraæoles, for example monoacetylmaleic acid hydrazide;
(d~ 0,N,N-trisubstituted hydroxylamines, such as 0-benzoyl-N,N-succinyl hydroxylamine, 0-acetyl-N,N-succinyl hydroxylamine, ~5 0-p-methoxybenzoyl N,N-succinyl-hydroxylamine, 0-p-nitrobenzoyl-N r N-succinyl-hydroxylamine and 0,N,N-triacetyl hydroxylamine;
(e) N,N'-diacyl-sulphurylamides, for example N,N'-dimethyl-N,N'-diacetyl-sulphurylamide and N,N'-diethyl-N,N'-dipropionyl sulphurylamidei (f) Triacylcyanurates, for example triacetyl cyanurate and tribenzoyl cyanurate;
(g) Carboxylic acid anhydrides, such as benzoic anhydride, m-chloro-benzoic anhydride, phthalic anhydride, 4-chloro-phthalic anhydride;
(h) Sugar esters, for example glucose pentaacetate;
(i) 1,3-diacyl-4,5-diacyloxy-imidazolidine, for example 1,3-diformyl-4,5-diacetoxy-imidazolidine, 1,3-diacetyl-4,5-diacetoxy-imidazolidine, 1,3-diacetyl-4,5-dipropionyloxy-imidazoline;
(j) Tetraacetylglycoluril and tetrapropionylglycoluril;
(k) Diacylated 2,5-diketopiperazine, such as 1,4-diacetyl-2,5-diketopiperazine, 1,4~dipropionyl 2,5-diketopiperazine and 1,4-dipropionyl-3,6-dimetyl-~5 2,5-diketopiperazine;
(1) Acylation products o~ propylenediurea or 2r2-dimethyl-~19~
- 16 - C.1303/1 propylenediurea (2,4,6,8-tetraaza-bicyclo-(3,3,1)-nonane-3,7-dione or its 9,9-dimethyl derivative), especially the tetraacetyl- or the tetrapropionyl-propylenediurea or their dimethyl derivatives;
(m) Carbonic acid esters, for example the sodium salts of p-(ethoxycarbonyloxy)-benzoic acid and p-(propoxy-carbonyloxy)-benzenesulphonic acid.
(n) ~-acyloxy-(N,N') polyacyl malonamides, such as D<-acetoxy-tN~N~) diacetyl malonamide.
The N~diacylated and ~,N'-polyacylatedamines mentioned under (a) are of special interest, particularly N,N,N',N'-tetra-acetyl-ethylenediamine (TAED).
It is preferred to use the activator in granular form, preferably wherein the activator is finely divided as described in our UK Patent Application No. 80 21979.
Specifically, it is preferred to have an activator of an average particle size of less than 150 micrometres, which gives significant improvement in bleach efficiency. The sedimentation losses, when using an activator with an average particle size of less than 150 /um, are substantially deGreased. Even better bleach performance is obtained if the average particle size of the activator is less than 100 /um. However, too small a particle size gives increased decomposition, dust-formation and handling problems, and although particle sizes below 100 /um can provide for an improved bleaching efficienc~, it is desirable that the activator should not have more than 20%
by weight of particles with a size of less than 50 /um.
On the other hand, the activator may have a certain amount of particles of a si~e greater than 150 /um, but it should not contain more than 5% by weight of particles ~' 300 /um, and not more than 20% by weight of particles > 200 /um, preferably > 150 /um. It is to be understood that these particle sizes refer to the activator ~91~
- 17 - ~.1303/1 present in the granules, and not to the granules themselves. The latter have a particle size, the major part of it ranging from 100 to 2000 /um, preferably 250 to 1000 /um. Up to 5% by weight of granules with a particle size of ~ 1700 /um and up to 10% by weight of granules ~ 250 /um is tolerable. The granules incorporating the activator, preferably in this finel~-divided form, may be obtained by granulating a suitable carrier material, such as sodium tripolyphosphate and/or potassium tripolyphosphate with activator particles of the required size. Other granulation methods, e.g. using organic and/or inorganic granulation aids, can also be usefully applied. The granules can be subsequently dried, if required.
Basically, any granulation process is appli~able, as long as the granule contains the activator, and as long as the other materials present in the granule do not negatively affect the activator.
It is particularly preferred to include in the detergent compositions a stabiliser for the bleach system, for example ethylene diamine tetramethylene phosphonate and diethylene triamine pentamethylene phosphonate. These stabilisers can be used in acid or salt form, especially in calcium, magnesium, zinc or aluminium salt form, as described in our UK Patent Application No. 2 048 930.
Apart from the components already mentioned, the detergent compositions of the invention can contain any of the conventional additives in the amounts in which such materials are normally employed in fabric washing detergent compositions. Examples of these additives include lather boosters such as alkanolamides, particularly the monoethanolamides derived from palm kernel fatty acids and coconut fatty acids; lather depressants such as al~yl - 1~91C~
~ C.1303/1 phosphates, silicones, or alkyl phosphonic acids incorporated in petroleum jelly, wax or mineral oil;
anti-redeposition agents such as sodium carboxymethyl-cellulose and cellulose ethers; fabric softening agents;
inor~anic salts such as sodium sulphate and sodium carbonate; and, usually present in very minor amounts, fluorescent agents, perfumes, enzymes such as proteases and amylases.
It may be desirable to include in the composition an amount of an alkali metal silicate, particularly sodium ortho-, meta- or pre~erably neutral or alkaline silicateO
The presence of such alkali metal silicates at levels of at least ~bout 1%, and preferably from about 5~ to about 15%
by weight of the composition, is advantageous in decreasing the corrosion of metal parts in washing machines, besides giving processing benefits and generally improved powder properties. The more highly alkaline ortho- and meta-silicates would normally only be used at lower amounts within this range, in admixture with the neutral or alkaline silicates.
The composition of the invention is preferably alkaline, but not too strongly alkaline as this could result in fabric damage and also be hazardous for domestic usage. In practice the composition should desirably give a pH of from about 8.5 to about 11 in use in aqueous wash solution. It is preferred in particular for domestic products to have a pH of from about 9.0 to about 10.5 as lower pH's tend to be less effective for optimum detergency building, and more highly alkaline products can be hazardous if misused. The pH is measured at the lowest normal usage concentration of 0.1% w/v of the product in water of 12H (Ca), (French permanen~ hardness, calcium only) at 50C so that a satisfactory degree of alkalinity can be assured in use at all normal product concentrations.
119~0~
- 19 - C.13~3/1 If necessary, up to 10% by weight of alkali metal carbonate, preferably sodium carbonate, may be included in order to raise the pH and to maintain adequate buffer capacity in the presence of acidic soils.
If carbonate or phosphates are present it may be desirable to include in the composition of the invention one or more antideposition agents, to decrease any tendency to form inorganic deposits on washed fabrics. The amount of any such antideposition agent is normally from about 0.1~ to about 5% by weight, preferably from about 0.2% to about 1.5~ by weight of the composition. The preferred antideposition agents are anionic polyelectrolytes, esp~cially polymeric aliphatic carboxylates, or orqanic phosphonates.
The detergent compositions of the invention should desirably be in free-flowing particulate, for example, powdered or granular form, and can be produced by any of the techniques commonly employed in the manufacture of such washing compositions, for example, by slurry-making and spray-drying processes. It is preferred that the process used to form the compositions should result in a product having a moisture content of not more than about 12%, more preferably from about 4% to about 10% by weight.
The detergent compositions of the invention may also be in the form of bars or tablets, or in liquid form.
The invention will now be illustrated by the following non-limiting Examples.
EXAMPLES
In the Examples that follow, the detergencies of wash liquors incorporating various builder systems were compared ~L191(~
- 20 - C.1303/1 by measuring the reflectance of a clay-soiled polyester/cotton test cloth before and after washing in the Tergotometer. The reflectances were measured using a Carl Zeiss Elrepho Reflectometer and the reflectance increase on washing (~R) was taken as a measure of detergency.
In each case a wash liquor was prepared using the ingredients stated below in the concentrations stated below, in 40FH (Ca)water. The wash liquor was allowed to equilibrate for 15 minutes. Test cloth pieces ~four,pieces per litre, each measuring 76.2 mm x 76.2 mm) were then added and a 20-minute wash at 80C, pH
10.0 and 55 rpm agitation was carried out, followed by a rinse in water of the same hardness as that of the water used to prepare the wash liquor.
The ingredients and concentrations were as follows:
g/litre Sodium C10-Cl3 linear alkylbenzene 0.135 sulphonate C14-C15 alcohol ethoxylate (11 EO) 0.09 Hardened tallow soap* 0.06 Alkaline silicate 0.15 Sodium sulphate 2.00 Detergent additive according to the invention (as specified in E~amples) 2.00-5.00 * The soap was included for lather control purposes and was present in addition to the soap included in the detergent additive according to the invention.
~ 21 C~1303/1 It will be seen that the detergent additive according to the invention was used at concentrations of from 2.00 to 5.00 g/litre, and the other components of the composition were used at a constant total concentration of ~.495 g/litre, so that the total concentration ranged from 4.495 to 7.495 g/litre. Thus the percentage of the total composition constituted by the detergent additive of the invention at each concentration of the latter was as follows:
10 ¦ Concentration I .
~ % detergent additive ¦ (of detergent ¦ (total) ¦ in composition additive 1 2~00 1 4.495 1 44.49 ¦ ~.50 ¦ 4.995 ¦ 50O05
3.00 1 5.495 1 54.60
4.00 1 6.495 1 61.59
5.00 1 7.495 1 66.71 .l All percentages given in the Examples are by weight and are based on the anhydrous materials.
The detergencies of compositions containing a ternary builder system (detergent additive) according to the invention were compared, in 40EH water at a range of concentrations, with those of control compositions containing single or binary builder systems. The aluminosilicate used was zeolite A, the soap was hardened tallow soap, and the NTA was in the form of its trisodium salt. The results were as follows:
~19~
- 22 - C.1303/1 Reflec a ce ~R
Concentration,_g/l ¦ 2.0 ¦ 2.5 ¦ 3.0 ¦ 4.0 ¦ 5.0 ¦
l______l______l______l______l______l Detergent Additive 60~ zeolite/25% soap/
15% NTA -- ¦ 17.3 ¦ 22.6 ¦ 26.1 ¦ 27.3 ¦ 27.5 ¦
8S% zeolite/15% NTA ¦ 15.2 ¦ 20.3 ¦ 24.8 ¦ 26.2 ¦ 27.3 ¦
75% zeolite/25~ soap ¦ 15.3 ¦ 18.1 ~ 20.9 ¦ 23.5 ¦ 25.4 ¦
100~ zeolite ¦ 14.8 ¦ 17.4 ¦ 19.8 ¦ 22.1 ¦ 24.3 ¦
The procedure of Example 1 was repeated using different proportions of zeolite, soap and NTA~ The results were as follows:
Reflectance ~R
_ _ _ Concentration, g/l ¦ 3.0 ¦ 4.0 l__________l__________l Detergent Additive l l l 70% zeolite/20% soap/10% NTA ¦ 24.8 ~ 28.3 90% zeolite/10% NTA ¦ 21.2 ¦ 24.1 80% zeolite/20~ soap ¦ 18.5 ¦ 24.0 100% zeolite ¦ 18.7 ¦ 22.4
The detergencies of compositions containing a ternary builder system (detergent additive) according to the invention were compared, in 40EH water at a range of concentrations, with those of control compositions containing single or binary builder systems. The aluminosilicate used was zeolite A, the soap was hardened tallow soap, and the NTA was in the form of its trisodium salt. The results were as follows:
~19~
- 22 - C.1303/1 Reflec a ce ~R
Concentration,_g/l ¦ 2.0 ¦ 2.5 ¦ 3.0 ¦ 4.0 ¦ 5.0 ¦
l______l______l______l______l______l Detergent Additive 60~ zeolite/25% soap/
15% NTA -- ¦ 17.3 ¦ 22.6 ¦ 26.1 ¦ 27.3 ¦ 27.5 ¦
8S% zeolite/15% NTA ¦ 15.2 ¦ 20.3 ¦ 24.8 ¦ 26.2 ¦ 27.3 ¦
75% zeolite/25~ soap ¦ 15.3 ¦ 18.1 ~ 20.9 ¦ 23.5 ¦ 25.4 ¦
100~ zeolite ¦ 14.8 ¦ 17.4 ¦ 19.8 ¦ 22.1 ¦ 24.3 ¦
The procedure of Example 1 was repeated using different proportions of zeolite, soap and NTA~ The results were as follows:
Reflectance ~R
_ _ _ Concentration, g/l ¦ 3.0 ¦ 4.0 l__________l__________l Detergent Additive l l l 70% zeolite/20% soap/10% NTA ¦ 24.8 ~ 28.3 90% zeolite/10% NTA ¦ 21.2 ¦ 24.1 80% zeolite/20~ soap ¦ 18.5 ¦ 24.0 100% zeolite ¦ 18.7 ¦ 22.4
Claims (19)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A detergent additive consisting of:
(a) at least 25% by weight of a crystalline or amorphous aluminosilicate cation-exchange material, (b) the balance consisting of (i) one or more water-soluble soaps of C8-C22 fatty acids, at least 60% by weight of the total soap being saturated material, (ii) nitrilotriacetic acid or a water-soluble salt thereof, the weight ratio of (i) to (ii) being from 3:1 to 1:3, and (i) being present in an amount of at least 12% by weight based on the total weight of (a) and (b)
(a) at least 25% by weight of a crystalline or amorphous aluminosilicate cation-exchange material, (b) the balance consisting of (i) one or more water-soluble soaps of C8-C22 fatty acids, at least 60% by weight of the total soap being saturated material, (ii) nitrilotriacetic acid or a water-soluble salt thereof, the weight ratio of (i) to (ii) being from 3:1 to 1:3, and (i) being present in an amount of at least 12% by weight based on the total weight of (a) and (b)
2. A detergent additive as claimed in Claim l, wherein the soap (i) is present in an amount of at least 15% by weight, based on the total weight of (a) and (b).
3. A detergent additive as claimed in Claim 1 or Claim 2, characterised in that at least 80% by weight of the soap (i) is saturated material.
4. A detergent additive as claimed in Claim 1 or Claim 2, characterised in that the soap (i) consists substantially wholly of saturated material.
5. A detergent additive as claimed in claim 1, wherein the soap (i) contains at least 5% by weight of material having a chain length of C18 and above and at least 1% of material having a chain length of C14 and below.
6. A detergent additive as claimed in Claim 5, wherein the soap (i) contains at least 60% by weight of material having a chain length of C18 and above and at least 1% of material having a chain length of C14 and below.
7. A detergent additive as claimed in Claim 5, wherein the soap (i) comprises hardened tallow soap and/or hardened rapeseed soap.
8. A detergent additive as claimed in Claim 5, wherein the soap (i) contains at least 60% of material having a chain length of C14 and below and at least 5% of material having a chain length of C18 and above.
9. A detergent additive as claimed in Claim 5, wherein the soap (i) comprises coconut soap and/or palm kernel soap.
10. A detergent additive as claimed in any one of Claims 1 to 3, wherein (ii) is an alkali metal salt of nitrilotriacetic acid.
11. A detergent additive as claimed in claim 1, wherein the aluminosilicate cation exchange material is a crystalline material having a unit cell of the formula Nax (A102) X- (Si°2) y zH2°
whPrein x and y are integers of at least 6, the ratio of x to y being in the range of 1:1 to 1:2; and z is such that the bound water content is from 10% to 28% by weight.
whPrein x and y are integers of at least 6, the ratio of x to y being in the range of 1:1 to 1:2; and z is such that the bound water content is from 10% to 28% by weight.
12. A detergent additive as claimed in Claim 11, wherein the aluminosilicate cation exchange material is a crystalline material having a unit cell of the formula Na12(Al02)12 (si°2)12.zH2°
wherein z is from 20 to 30.
wherein z is from 20 to 30.
13. A detergent additive as claimed in any one of Claims 1 to 3, wherein it contains from 20 to 50% by weight, in total, of (i) and (ii).
14. A detergent additive as claimed in any one of Claims 1 to 3, characterised in that the weight ratio of (i) to (ii) is from 3:1 to 1:1.
15. A detergent composition comprising from 3 to 90% by weight of at least one synthetic detergent-active material and from 10 to 97% by weight of a detergent additive as claimed in Claim 1.
16. A detergent composition as claimed in Claim 15, which contains, in total, from 5 to 40% by weight of (i) and (ii) .
\
\
17. A detergent composition as claimed in Claim 15, which contains from 3 to 20% by weight of (i).
18. A detergent composition as claimed in Claim 15, characterised in that it contains from 1 to 15, by weight of (ii).
19. A detergent composition as claimed in Claim 15, which contains not more than 10% by weight of inorganic phosphate.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8121837 | 1981-07-15 | ||
| GB8121837 | 1981-07-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1191068A true CA1191068A (en) | 1985-07-30 |
Family
ID=10523262
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000407291A Expired CA1191068A (en) | 1981-07-15 | 1982-07-14 | Detergent additives and detergent compositions containing them |
| CA000407293A Expired CA1197156A (en) | 1981-07-15 | 1982-07-14 | Detergent additives and detergent compositions containing them |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000407293A Expired CA1197156A (en) | 1981-07-15 | 1982-07-14 | Detergent additives and detergent compositions containing them |
Country Status (11)
| Country | Link |
|---|---|
| EP (2) | EP0070190B1 (en) |
| JP (2) | JPS5823896A (en) |
| AT (2) | ATE15499T1 (en) |
| AU (2) | AU554225B2 (en) |
| BR (2) | BR8204091A (en) |
| CA (2) | CA1191068A (en) |
| DE (2) | DE3266194D1 (en) |
| DK (2) | DK314782A (en) |
| NO (2) | NO822434L (en) |
| NZ (2) | NZ201213A (en) |
| ZA (2) | ZA825005B (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9008013D0 (en) * | 1990-04-09 | 1990-06-06 | Unilever Plc | High bulk density granular detergent compositions and process for preparing them |
| US5508258A (en) * | 1990-08-03 | 1996-04-16 | Henkel Kommanditgesellschaft Auf Aktien | Use of surface-active alpha-sulfo-fatty acid di-salts in water and oil based drilling fluids and other drill-hole treatment agents |
| GB9022660D0 (en) * | 1990-10-18 | 1990-11-28 | Unilever Plc | Detergent compositions |
| AU2005280915B2 (en) * | 2004-09-06 | 2010-10-07 | Furukawa Techno Material Co., Ltd. | Surfactant-Based Composition |
| JP5388260B2 (en) * | 2006-03-03 | 2014-01-15 | 株式会社古河テクノマテリアル | Water-added fire extinguisher |
| JP5207161B2 (en) * | 2006-08-10 | 2013-06-12 | ディバーシー株式会社 | Method of supplying detergent to automatic dishwasher, tablet detergent composition for automatic dishwasher used therein, and washing method using the same |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE419975C (en) * | 1973-04-13 | 1986-08-18 | Henkel Kgaa | DETERGENTS AND / OR BLENDS CONTAINING A CRYSTALLINE WATER-INSULATED SILICATE PROCEDURE FOR ITS PREPARATION AND USE |
| US4605509A (en) * | 1973-05-11 | 1986-08-12 | The Procter & Gamble Company | Detergent compositions containing sodium aluminosilicate builders |
| DE2333356C3 (en) * | 1973-06-30 | 1982-03-11 | Henkel KGaA, 4000 Düsseldorf | laundry detergent |
| AT335030B (en) * | 1974-01-14 | 1977-02-25 | Henkel & Cie Gmbh | METHOD OF WASHING TEXTILES AND MEANS OF CARRYING OUT THE METHOD |
| JPS5328163B2 (en) * | 1974-05-30 | 1978-08-12 | ||
| US3985669A (en) * | 1974-06-17 | 1976-10-12 | The Procter & Gamble Company | Detergent compositions |
| AT375395B (en) * | 1974-10-04 | 1984-07-25 | Henkel Kgaa | METHOD FOR WASHING OR BLEACHING TEXTILES AND MEANS THEREOF |
| AT338948B (en) * | 1974-10-10 | 1977-09-26 | Henkel & Cie Gmbh | POWDERED DETERGENTS AND CLEANING AGENTS AND METHOD FOR THEIR PRODUCTION |
| JPS5228507A (en) * | 1975-08-29 | 1977-03-03 | Nippon Oil & Fats Co Ltd | Detergent composition |
| JPS52117908A (en) * | 1976-03-31 | 1977-10-03 | Nitsusan Setsuken Kk | Detergent composition |
| GB2040981B (en) * | 1977-06-21 | 1982-08-25 | Procter & Gamble | Low-phosphate detergent composition for fabric washing |
| IT1160682B (en) * | 1977-10-14 | 1987-03-11 | Po Corp. | DETERGENT COMPOSITIONS WITH SILANO-ZEOLITE ADJUVANT |
| CA1137076A (en) * | 1978-12-13 | 1982-12-07 | John R. Bauer | Fluid spray mixer - reactor system |
| JPS55108496A (en) * | 1979-02-13 | 1980-08-20 | Nippon Gousei Senzai Kk | Detergent composition |
| US4265777A (en) * | 1980-04-17 | 1981-05-05 | The Procter & Gamble Company | Detergent compositions containing an aluminosilicate detergency builder and an unsaturated fatty acid soap |
-
1982
- 1982-07-09 NZ NZ201213A patent/NZ201213A/en unknown
- 1982-07-09 NZ NZ201212A patent/NZ201212A/en unknown
- 1982-07-13 EP EP82303674A patent/EP0070190B1/en not_active Expired
- 1982-07-13 AU AU85984/82A patent/AU554225B2/en not_active Ceased
- 1982-07-13 DE DE8282303676T patent/DE3266194D1/en not_active Expired
- 1982-07-13 AU AU85985/82A patent/AU8598582A/en not_active Abandoned
- 1982-07-13 AT AT82303676T patent/ATE15499T1/en not_active IP Right Cessation
- 1982-07-13 AT AT82303674T patent/ATE16818T1/en not_active IP Right Cessation
- 1982-07-13 DE DE8282303674T patent/DE3267784D1/en not_active Expired
- 1982-07-13 EP EP82303676A patent/EP0070192B2/en not_active Expired - Lifetime
- 1982-07-14 DK DK314782A patent/DK314782A/en not_active Application Discontinuation
- 1982-07-14 CA CA000407291A patent/CA1191068A/en not_active Expired
- 1982-07-14 CA CA000407293A patent/CA1197156A/en not_active Expired
- 1982-07-14 NO NO822434A patent/NO822434L/en unknown
- 1982-07-14 BR BR8204091A patent/BR8204091A/en unknown
- 1982-07-14 DK DK314982A patent/DK314982A/en not_active Application Discontinuation
- 1982-07-14 ZA ZA825005A patent/ZA825005B/en unknown
- 1982-07-14 NO NO822433A patent/NO822433L/en unknown
- 1982-07-14 BR BR8204092A patent/BR8204092A/en not_active IP Right Cessation
- 1982-07-14 ZA ZA825006A patent/ZA825006B/en unknown
- 1982-07-15 JP JP57123749A patent/JPS5823896A/en active Granted
- 1982-07-15 JP JP57123750A patent/JPS5823897A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| CA1197156A (en) | 1985-11-26 |
| ATE15499T1 (en) | 1985-09-15 |
| NO822434L (en) | 1983-01-17 |
| JPS5823896A (en) | 1983-02-12 |
| DE3267784D1 (en) | 1986-01-16 |
| DK314982A (en) | 1983-01-16 |
| EP0070192B1 (en) | 1985-09-11 |
| AU554225B2 (en) | 1986-08-14 |
| ZA825006B (en) | 1984-02-29 |
| EP0070190B1 (en) | 1985-12-04 |
| DE3266194D1 (en) | 1985-10-17 |
| JPS6116315B2 (en) | 1986-04-30 |
| AU8598482A (en) | 1983-01-20 |
| DK314782A (en) | 1983-01-16 |
| BR8204091A (en) | 1983-07-05 |
| AU8598582A (en) | 1983-01-20 |
| ATE16818T1 (en) | 1985-12-15 |
| BR8204092A (en) | 1983-07-05 |
| JPH045720B2 (en) | 1992-02-03 |
| NO822433L (en) | 1983-01-17 |
| NZ201213A (en) | 1985-07-31 |
| ZA825005B (en) | 1984-02-29 |
| JPS5823897A (en) | 1983-02-12 |
| EP0070192A1 (en) | 1983-01-19 |
| EP0070192B2 (en) | 1990-01-17 |
| EP0070190A1 (en) | 1983-01-19 |
| NZ201212A (en) | 1985-08-16 |
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