NZ224863A - Surfactant system containing anionic and alkoxylated nonionic surfactants - Google Patents
Surfactant system containing anionic and alkoxylated nonionic surfactantsInfo
- Publication number
- NZ224863A NZ224863A NZ224863A NZ22486388A NZ224863A NZ 224863 A NZ224863 A NZ 224863A NZ 224863 A NZ224863 A NZ 224863A NZ 22486388 A NZ22486388 A NZ 22486388A NZ 224863 A NZ224863 A NZ 224863A
- Authority
- NZ
- New Zealand
- Prior art keywords
- weight
- surfactant
- alkyl
- composition according
- sodium
- Prior art date
Links
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
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
- C11D17/0026—Structured liquid compositions, e.g. liquid crystalline phases or network containing non-Newtonian phase
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/22—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Description
<div id="description" class="application article clearfix">
<p lang="en" class="printTableText">New Zealand Paient Spedficaiion for Paient Number £24863 <br><br>
n <br><br>
22 4 8 6 3 <br><br>
^ *^^ALAND <br><br>
PATENTS ACT, 1953 <br><br>
/ v * <br><br>
No.: Date: <br><br>
COMPLETE SPECIFICATION <br><br>
LIQUID DETERGENT COMPOSITIONS <br><br>
j-- —11 We, ALBRIGHT & WILSON LIMITED, a British company, of 210-222 s Hagley Road West, Oldbury, Warley, West Midlands, England hereby declare the invention for which I / we pray that a patent may be granted to me-/us, and the method by which it is to be performed, to be particularly described in and by the following statement: - <br><br>
- 1 - <br><br>
(followed by page la) <br><br>
22 4 8 6 3 <br><br>
-let' <br><br>
This invention relates to liquid detergent compositions and preferably compositions having a stable spherulitic structure and comprising a substantial proportion of non-ionic surfactant. The invention is especially applicable to the formulation of liquid detergent compositions having a controlled foaming character e.g. suitable for use in a front loading washing machine. It is also of value in preparing compositions suitable for use in low temperature wash regimes. <br><br>
In formulating liquid laundry detergents, a good balance of mobility and high pay load of useful ingredients is most readily obtained if the surfactants can be constrained to adopt a spherulitic structure by the presence of an appropriate concentration of an electrolyte which salts surfactants out of aqueous micellar solution and forms them into spherulites, which are believed to consist of a number of concentric shells, each comprising a curved surfactant bilayer, alternating with shells of aqueous electrolyte solution. When the spherulites are sufficiently closely packed, a stable structured liquid is formed, capable of suspending solid particles of builder. Compositions of this type are discussed in detail in our GB-A-2 153 380, the disclosure of which is incorporated herein by reference. <br><br>
Relatively few single surfactants are known which are capable of forming stable spherulitic compositions on their own. They are characterised by very bulky hydrophobic groups having a large cross-sectional area relative to the hydrophilic groups, e.g. some secondary or branched chain alkyl benzene sulphonates such as sodium dodeca-6-yl benzene sulphonate, dialkyl sulphosuccinates and some olefin sulphonates. Generally these surfactants are expensive and exhibit poor detergency. However spherulites can more readily be obtained using mixtures of surfactants. In particular mixtures of <br><br>
22 A 8 6 3 <br><br>
-2- <br><br>
linear alkyl benzene sulphonates with alkyl ether sulphates, amine-oxides, or alkanolamides are all capable of forming stable spherulitic compositions and exhibit relatively cost-effective detergency, at least for natural fibres. <br><br>
Such compositions however have two disadvantages, which apply, respectively to those markets where front loading washing machines are commonly used, and to markets in which washing is carried out at low or ambient temperatures and/or the washload includes a high proportion of synthetic fibre. <br><br>
Firstly the surfactant mixtures hitherto found to give stable spherulites have been inherently high foaming systems. To formulate detergent compositions suitable for use in front loading washing machines, it has therefore been necessary to include relatively large amounts of expensive antifoams such as silicones. In addition to the cost, silicones have a less than ideal performance in that they tend to give too low a foam in the wash but some residual foam in the rinse. The consumer gets the impression that the detergent is not very effective and is not rinsing out properly. <br><br>
Secondly it has not proved possible to make stable spherulitic compositions containing significant levels of ethoxylated non-ionic detergent surfactants. Mixtures containing the latter are generally more cost-effective for cleaning synthetic fibres and give improved performance at low wash temperatures e.g. below 40'C. The detergent surfactants are generally defined as those having an HLB between 12 and 15. Surfactants outside this HLB range are not normally considered to be detergents. <br><br>
A further problem which may arise when liquid detergents are exported or sold at a point remote from the source of surfactant is <br><br>
22 4 8 6 3 <br><br>
-3- <br><br>
the cost of transporting the water and builder content of the liquid detergent. It is convenient to be able to transport the active material as a concentrate in a form suitable for blending and dilution at a site closer to the point of sale. Such compositions need to be pourable and non-separating, but also to be relatively the cost of transporting the water and builder content of the liquid detergent. It is convenient to be able to transport the active material as a concentrate in a form suitable for blending and dilution at a site closer to the point of sale. Such compositions need to be pourable and non-separating, but also to be relatively concentrated. Many bulk surfactants, however, are difficult to concentrate above about 30% due to the formation of immobile M phases. <br><br>
We have now discovered that certain mixtures of linear alkyl benzene sulphonates with non-ionic surfactants having an HLB of less than 12 form stable spherulitic compositions with high levels of wash performance on both natural and synthetic fibres and have substantially reduced foaming tendencies, and/or improved wash performance at low temperatures. <br><br>
We have further discovered that when such mixtures are concentrated to appropriate concentrations within the range 25 to 80%, non-separating pourable spherulitic and/or G phase compositions are obtained which can readily be diluted or blended with other detergent ingredients and which are relatively cheap to transport and store. <br><br>
Our invention, according to one embodiment, provides a surfactant system for use in a liquid detergent consisting essentially of: an active mixture of (a) at least 50% by weight, based on the total weight of the surfactants present, of anionic surfactants comprising at least 20%, based on the total weight of <br><br>
'■< <br><br>
224863 <br><br>
% <br><br>
X -4- <br><br>
| the surfactants present, of an alkyl benzene sulphonate, and (b) at <br><br>
1 least 2% by weight, based on the total weight of the surfactants j O present, of an alkoxylated non-ionic surfactant having an HLB below j 12; and sufficient water to provide a non-separating pourable i <br><br>
| spherulitic or G phase composition. <br><br>
t i } <br><br>
{ Preferably the surfactant concentration of the surfactant <br><br>
] (3 system is greater than 28%, e.g. greater than 30% and preferably <br><br>
| between 30 and 80%. Usually the surfactant concentration is <br><br>
| greater than 35% e.g. 40 to 75% especially 50 to 70% by weight. <br><br>
The surfactant system preferably consists essentially of surfactant and water together with such traces of sodium sulphate as are unavoidably present as an impurity in the anionic surfactant. It is, however, possible to include minor proportions of non-surfactant electrolytes in order to modify the viscosity and/or phase structure of the composition. We generally prefer that such electrolytes be present in proportions of less than 10%, preferably less than 5%, usually less than 2%, e.g. less than 1% of the total weight of the surfactant system. The presence of organic solvents is not preferred. <br><br>
j According to a further embodiment our invention provides a liquid detergent composition comprising water,sufficient of an active mixture as aforesaid to provide a total surfactant concentration of from 5 to 25%, by weight of the composition; and a dissolved surfactant desolubilising electrolyte in a concentration adapted to provide a non-sedimenting spherulitic composition. Preferably the liquid detergent composition of our invention additionally comprises suspended solid particles of a builder. <br><br>
The alkyl benzene sulphonate preferably has an average of from 10 to 14 aliphatic carbon atoms, e.g. 12, and is preferably a <br><br>
H <br><br>
224863 <br><br>
-5- <br><br>
linear alkyl benzene sulphonate. Particularly preferred are alkyl benzene sulphonates containing a broad range of different homologues and isomers. <br><br>
For low foam use we prefer that the anionic surfactant comprises at least one mono-and/or di-alkyl phosphate ester in a proportion of up to 50% e.g. 2 to 40%, preferably 5 to 30% especially 10 to 20% of the total weight of the anionic surfactant present. <br><br>
The anionic surfactant may additionally or alternatively comprise other sulphonated and/or sulphated surfactants and/or carboxylates. For instance the anionic surfactant may comprise a mixture of alkyl benzene sulphonate with from 5 to 100%, preferably 10 to 50% e.g. 15 to 30% of a Cg.gg (preferably Cj0-14) alkyl sulphate, based on the weight of alkyl benzene sulphonate. Where low temperature performance is important and low foam is not required the composition preferably comprises from 5 to 150%, preferably 20 to 120% e.g. 50 to 110% of Cg_20 (preferably Cjg.jg) alkyl polyalkyleneoxy sulphate based on the weight of alkylbenzene sulphonate. The alkyl polyalkyleneoxy sulphate preferably comprises an average of from 1 to 10 e.g. 1.5 to 5 molar parts of ethylene oxide. Other anionic surfactants which may be present include olefin sulphonates, parafin sulphonates, fatty acid sulphonates, sulphosuccinates, sulphosuccinamates and soaps. The counter ion of the anionic surfactant may be sodium, lithium, potassium, ammonium, or a lower alkyl ammonium or mono-di- or tri-alkanolammonium or a mixture of such ions. <br><br>
The non-ionic surfactant is preferably an ethoxylated alcohol but may alternatively be an ethoxylated carboxylic acid, alkyl amine, alkanolamide, alkylphenol, or ester such as an ethoxylated glyceryl, sorbitan, phosphate <br><br>
224863 <br><br>
r> <br><br>
-6- <br><br>
The alkyl groups of the non-ionic surfactant may be straight chain and primary, but comprise preferably at least some branched chain alkyl groups. It is often found that the greater the proportion of branched chain alkyl groups and the amount of branching, the more effective the detergency of the product. <br><br>
The alkyl groups of the non-ionic surfactant have an average of from 8 to 20, preferably 10 to 18 carbon atoms. For example ethoxylated Cg_j5 e.g. Cg_n or Cj2-13 branched chain alcohols are especially preferred from the point of view of detergency, but ethoxylated Cjg.jg linear alcohols give superior foam inhibition. For the lower temperature wash conditions, Cg.^5 alkyl groups are preferred. <br><br>
The number of ethylene oxide groups is selected, according to the alkyl chain length, to provide the desired HLB. Typically there are from 1 to 12, e.g. 2 to 8, ethylene oxide groups. It is possible to replace one or more of the ethylene oxide groups with propylene oxide. The HLB of the non-ionic surfactant is preferably from 2 to 12 e.g. 3 to 10 especially 3.5 to 8. <br><br>
We prefer ethoxylates of feedstocks containing at least 20%, more preferably at least 30%, especially at least 50%, e.g. at least 60%, branched chain alcohols. <br><br>
The non-ionic surfactant may comprise a proportion of free ^8-22 alc°hol- This is especially preferred for low foam compositions. The latter typically contain C14 to 22 fatty alcohols, e.g. in proportions up to 100% by weight of the total anionic surfactant. High foam, low temperature compositions may contain minor proportions of unethoxylated fatty alcohols, corresponding to the feed stock of the fatty alcohol ethoxylate. The latter are usually Cg to jg e.g. Cg.jj alcohols. We do not <br><br>
22 A 8 6 3 <br><br>
-7- <br><br>
exclude the presence of polyethylene glycol in the nonionic surfactant. <br><br>
Any fatty alcohol or polyethylene glycol are deemed to be included in the total ethoxylated non-ionic surfactant when estimating the HLB of the latter or in defining relative proportions of non-ionic surfactant. In the case of ethoxylated fatty alcohols the HLB may be taken for the purpose of this specification as being one fifth of the weight percentage of ethylene oxide based on the weight of non-ionic surfactant. <br><br>
The total proportion of surfactant is from 5 to 25% of the liquid of the total weight detergent composition. For low foam applications the total proportion of surfactant is preferably less than 20%, e.g. less than 14%, most preferably 5 to 12% based on the weight of the liquid detergent composition. However for low temperature use, where low foam is not a requirement, higher concentrations of total surfactant are preferred e.g. greater than 18%, especially 20 to 25% based on the total weight of the liquid detergent composition. <br><br>
The detergent composition of our invention comprises an electrolyte in a quantity sufficient to provide a non-sedimenting spherulitic composition. "Electrolyte" is used herein to refer to any water-soluble compound which is dissolved in the composition, which ionises in solution and which is capable of salting the surfactants out of micellar solution to form a spherulitic composition, but which is not itself a surfactant. The electrolyte may, preferably, comprise any of the water-soluble builders, or a dissolved portion of a sparingly soluble builder. Examples of suitable electrolytes therefore include citrates, orthophosphates, nitrilotriacetates, condensed phosphates such as pyrophosphates, <br><br>
22 4 8 6 3 <br><br>
-8- <br><br>
tripolyphosphates or tetraphosphates, soluble phosphate glasses such as hexametaphosphates, carbonates, silicates, phosphonates, <br><br>
such as acetodiphosphonates, aminotris(methylene phosphonates), <br><br>
ethylene diamine tetrakis(methylene phosphonates), diethylene triamine pentakis(methylene phosphonates) and higher homologues of the same series, and ethylenediamine tetracetates. <br><br>
It is possible to use as electrolyte, or part thereof, a buffer such as a borate, or less preferably a non-functional salt such as a chloride, bromide, iodide, nitrate or the like. Organic electrolytes such as formate or acetate may also be present. <br><br>
Sulphate is normally present in minor amounts as an impurity of the anionic surfactant, but may give rise to undesirable crystallisation in amounts greater than about 3%. We therefore prefer to avoid the use of higher concentrations of sulphate. <br><br>
The cationic portion of the electrolyte is preferably an alkali metal, e.g. lithium, potassium or, more preferably, sodium. <br><br>
The total concentration of dissolved electrolyte is preferably greater than 1%, typically 2 to 12%, depending upon the concentration of surfactant and the total proportion of non-ionic to anionic. Higher concentrations of surfactant and/or higher proportions of non-ionic surfactant require lower concentrations of electrolyte to form non-separating, spherulitic compositions. If the concentration of surfactant and/or the proportion of non-ionic surfactant is sufficiently high, any adventitious sodium sulphate may be sufficient to ensure a stable spherulitic composition without the adition of extra electrolyte. <br><br>
The builder is preferably sodium tripolyphosphate and is preferably present in excess of its solubility, as suspended solid <br><br>
7248 <br><br>
-9- <br><br>
particles. Alternatively or additionally the composition may contain zeolites and/or solid particles of any of the builders referred to above under the discussion of electrolytes. <br><br>
The low-foaming compositions of our invention containing phosphate esters have been found to prevent excessive foaming but not to suppress foaming entirely at the wash stage, giving visible confirmation that the detergent is present and acting. There is however little or no foaming in the rinse water. <br><br>
It is possible, but less preferred, to add other foam suppressing agents such as Cjg.jg fatty alkanolamides and/or hydrocarbons in addition to or instead of the phosphate ester. We prefer, however, not to use silicones as the antifoams, although it is possible, according to our invention, to achieve effective foam suppression with reduced proportions of silicone antifoam compared with those conventionally used. Minor amounts of silicone may be added as protective agent if it is desired to include enzymes in the formulation, for example as described in European Patent Application Publication No. 295021. <br><br>
Detergent compositions of our invention may contain the usual minor ingredients. Preferably these include an anti-redeposition agent such as sodium carboxymethyl cellulose, in conventional amounts, an optical brightener and perfumes and/or colouring. The compositions may contain suspended particles of fabric softeners such as bentonite or synthetic clays, or may generally contain any of the other minor ingredients, builders and electrolytes listed in our aforesaid GB-A-2153380 and in substantially the same proportions. <br><br>
? 2 4 8 6 3 <br><br>
■n <br><br>
-10- <br><br>
A specially preferred liquid detergent composition for low foam use comprises: water; from 4 to 10%, preferably 5 to 8% of Cl2-14 ^near alkyl benzene sulphonate; from 0.5 to 4%, preferably 1 to 3% of Cjq_j4 alkyl sulphate; from 0.5 to 4%, preferably 1 to 3% of an ethoxylated alcohol said alcohol having from 10 to 14, preferably 11 to 13 carbon atoms and said ethoxylated alcohol having an average of from 1 to 5, preferably from 2 to 4 ethyleneoxy group per molecule; and from 20 to 30% e.g. 24 to 27% of sodium tripolyphosphate; wherein all proportions are by weight based on the total weight of the composition. The above preferred compositon will normally contain conventional proportions of soil suspending agent, such as carboxymethyl cellulose, optical brightening agents and perfumes. It preferably contains minor amounts e.g. O.l to 2% each of sodium silicate, an alkanolamine such as triethanolamine and/or of phosphonate. It may optionally contain antifoams such as silcones and/or phosphate esters, fabric softeners, such as bentonite, enzymes such as proteases and/or lipases, preferably dispersed in a protective medium such as silicone and preservatives such as formaldehyde. <br><br>
^ A further type of preferred composition, where low foam is not <br><br>
•w a requirement, but where washing efficiency at low temperatures is an important consideration, comprises: water; from 6 to 12 e.g. 7 to 1C« sodium linear Cjq-14 alkyl benzene sulphonate; optionally but preferably from 6 to 12 e.g. 7 to 10% sodium Cj^O (preferably Cie-ig) alkyl polyethyleneoxy sulphate having an average of from 1 ^ to 5 e.g. 2 to 4 ethyleneoxy groups per molecule; from 1 to 8% <br><br>
preferably 2 to 7% of Cg.jg (preferably Cg.jj) alcohol ethoxylate having an average of from 1 to 5.5. e.g. 2 to 5 ethylene oxide groups per molecule; and from 15 to 30%, preferably 19 to 26% of sodium tripolyphosphate. The composition preferably contains the usual minor ingredients, such as soil suspending agent, optical brightner and perfume, in conventional amounts. <br><br>
721863 <br><br>
-11- <br><br>
o o <br><br>
The invention will be illustrated by the following examples, each of which was made by mixing the ingredients in the percentages by weight based on the total composition in the following tables, with the balance in each case water. In each case the surface active ingredients i.e. those components listed in the tables down to and including the Cjg-jg alcohol in the case of examples 1 to 18, were mixed together with sufficient water to form pourable, turbid mixtures having active concentrations between 30 and 50% by weight. In each case samples were centrifuged at 20,000g for 90 minutes to determine the optimum concentrations, at which no separation could be observed. <br><br>
The resulting pourable non-separating aqueous spherulitic or lamellar compositions were storable. The aqueous active mixtures could also be perfumed and/or combined with the appropriate proportion of carboxymethyl cellulose and/or optical brightening agent and/or phosphonate, with adjustment of concentration when required. <br><br>
Finally the active concentrate was mixed with the builder (sodium tripolyphosphate, and/or zeolite) and sufficient water to provide the desired final composition. <br><br>
Each of Examples 1 to 18 provided a stable non-sedimenting spherulitic composition having foaming characteristics suitable for use in front loading washing machines and giving good washing performance with both natural and synthetic fibres. <br><br>
The compositions gave moderate, controlled foaming during the wash cycle and little or no foaming during the rinse cycles. <br><br>
Eamples 19 to 25 all gave non-sedimenting spherulitic compositions with good low temperature wash performance. <br><br>
Table 1 <br><br>
22 4 8 6 3 <br><br>
•12- <br><br>
Example No <br><br>
1 I 2 I 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 <br><br>
r^. <br><br>
Sodium Cjo-14 linear alkyl benzene sulphonate <br><br>
Ci2_is alcohol 3 mole ethoxylate <br><br>
Mixed mono and di <br><br>
C16-18 a1kyl phosphate cl6-18 alc°h°l <br><br>
Sodium <br><br>
Tripolyphosphate <br><br>
Zeolite A. <br><br>
Optical Brightening agent. <br><br>
Sodium <br><br>
Carboxymethyl Cellulose. <br><br>
Sodium ethylenediamine tetrakis (metheno-phosphonate) <br><br>
Perfume. <br><br>
5.01 4.8| 5.51 5.41 5.51 5.81 5.51 5.51 5.01 5.0 <br><br>
2.0 <br><br>
0.8 <br><br>
0.8 <br><br>
30.0 <br><br>
0.15 <br><br>
0.1 <br><br>
0.5 <br><br>
0.35 <br><br>
1.9 <br><br>
1.9 <br><br>
23.8 <br><br>
4.8 <br><br>
0.19 <br><br>
0.1 <br><br>
0.48 <br><br>
0.38 <br><br>
3.2 <br><br>
2.2 <br><br>
28.1 <br><br>
0.23 <br><br>
0.11 <br><br>
0.56 <br><br>
0.45 <br><br>
2.9 <br><br>
2.0 <br><br>
24.4 <br><br>
2.4 <br><br>
0.20 <br><br>
0.1 <br><br>
0.5 <br><br>
0.4 <br><br>
3.0 <br><br>
2.0 <br><br>
25.0 <br><br>
0.20 <br><br>
0.1 <br><br>
0.5 <br><br>
0.4 <br><br>
3.3 <br><br>
2.2 <br><br>
27.2 <br><br>
0.20 <br><br>
0.1 <br><br>
0.5 <br><br>
0.4 <br><br>
4.0 <br><br>
2.0 <br><br>
20.0 <br><br>
7.3 <br><br>
0.20 <br><br>
0.1 <br><br>
0.5 <br><br>
0.4 <br><br>
4.0 <br><br>
2.0 <br><br>
20.0 <br><br>
7.3 <br><br>
0.20 <br><br>
0.1 <br><br>
1.0 <br><br>
0.4 <br><br>
1.0 <br><br>
1.0 <br><br>
1.0 <br><br>
31.0 <br><br>
0.15 <br><br>
0.5 <br><br>
0.35 <br><br>
2.0 <br><br>
1.0 <br><br>
1.0 <br><br>
30.0 <br><br>
0.15 <br><br>
0.5 <br><br>
0.35 <br><br>
& <br><br>
m <br><br>
22 4 8 6 3 <br><br>
s~ <br><br>
% f>\ <br><br>
1 <br><br>
13- <br><br>
Table 2 <br><br>
a o <br><br>
Example No. <br><br>
1 11 <br><br>
12 <br><br>
13 <br><br>
14 <br><br>
15 <br><br>
16 <br><br>
17 <br><br>
18 <br><br>
Sodium Cjq-14 Linear alkyl benzene Sulphonate. <br><br>
| 6.0 <br><br>
1 <br><br>
i <br><br>
5.0 <br><br>
5.0 <br><br>
5.0 <br><br>
5.0 <br><br>
5.0 <br><br>
5.0 <br><br>
5.0 <br><br>
C12_15 alcohol 3 mole ethoxylate. <br><br>
1 <br><br>
| 2.0 <br><br>
1 <br><br>
1 <br><br>
1.0 <br><br>
1.5 <br><br>
Nonyl phenol, 9 mole ethoxylate. <br><br>
1 <br><br>
1 1 <br><br>
1 <br><br>
1.0 <br><br>
1.5 <br><br>
1.0 <br><br>
1.5 <br><br>
Nonyl Phenol, 12 mole ethoxylate. <br><br>
1 <br><br>
1 1 <br><br>
I <br><br>
1.0 <br><br>
*"12-18 alc°hol, 8 mole ethoxylate. <br><br>
1 <br><br>
1 1 <br><br>
1 <br><br>
2.0 <br><br>
1.0 <br><br>
Mixed mono and di Cjg.jg alkyl phosphate. <br><br>
1 <br><br>
| 1.0 1 <br><br>
I <br><br>
2.0 <br><br>
2.0 <br><br>
2.0 <br><br>
2.0 <br><br>
2.0 <br><br>
1.7 <br><br>
1.7 <br><br>
Cis_18 alcohol. <br><br>
1 <br><br>
| 1.0 <br><br>
1 <br><br>
Sodium Tripolyphosphate. <br><br>
1 <br><br>
127.0 <br><br>
i <br><br>
28.0 <br><br>
30.0 <br><br>
28.0 <br><br>
28.0 <br><br>
28.0 <br><br>
25.0 <br><br>
25.0 <br><br>
Zeolite A. <br><br>
1 <br><br>
1 <br><br>
i <br><br>
4.7 <br><br>
4.7 <br><br>
Optical Brightening agent <br><br>
1 <br><br>
|0.15 <br><br>
i <br><br>
0.2 <br><br>
0.2 <br><br>
0.2 <br><br>
0.2 <br><br>
0.2 <br><br>
0.2 <br><br>
0.2 <br><br>
Sodium Carboxymethyl Cellulose <br><br>
1 <br><br>
1 0.1 1 <br><br>
i <br><br>
0.1 <br><br>
0.1 <br><br>
0.1 <br><br>
0.1 <br><br>
0.1 <br><br>
0.1 <br><br>
0.1 <br><br>
Sodium ethylenediamine tetra-kis (methenophosphonate). <br><br>
1 <br><br>
| 0.5 <br><br>
1 <br><br>
1 <br><br>
0.5 <br><br>
0.5 <br><br>
0.5 <br><br>
0.5 <br><br>
0.5 <br><br>
0.5 <br><br>
0.5 <br><br>
Perfume. <br><br>
1 <br><br>
|0.35 <br><br>
0.4 <br><br>
0.4 <br><br>
0.4 <br><br>
0.4 <br><br>
0.4 <br><br>
0.4 <br><br>
0.4 <br><br></p>
</div>
Claims (22)
1. A surfactant system for use in a liquid detergent consisting essentially of: an active mixture of (a) at least 50% by weight, based on the total weight of the surfactants present, of anionic surfactants comprising at least 20% by weight, based on the total weight of the surfactants present, of an alkyl benzene sulphonate and (b) at least 2% by weight, based on the total weight of surfactants present,of an alkoxylated non-ionic surfactant having an HLB below 12; and sufficient water to provide a non-separating, pourable, spherulitic or G phase composition.<br><br>
2. A surfactant system according to claim 1 containing less than 10% by weight of the surfactant system, of non-surfactant electrolyte.<br><br>
3. A surfactant system according to claim 2 wherein the proportion of non-surfactant electrolyte is less than 5% by weight, based on the total weight of the surfactant system.<br><br>
4. A surfactant system according to any foregoing claim substantially free from organic solvents.<br><br>
5. A surfactant system according to any foregoing claim containing between 30 and 80% by weight of said active mixture, based on the total weight of the surfactant system.<br><br>
6. A liquid detergent composition comprisinq: water; sufficient of an active mixture as specified in any of claims 1 to 5 to provide a total surfactant concentration of from 5 to 25% by weight of the composition; and sufficient, dissolved, surfactant-desolubilising electrolyte to provide a non-sedimenting spherulitic composition.<br><br>
7. A liquid detergent composition according to claim 6 containing suspended solid particles of builder.<br><br> 2 8 NOV I99|1<br><br> rV<br><br> - 16 -<br><br> 724863<br><br>
8. A composition according to any foregoing claim wherein the alkyl benzene sulphonate is a linear ^12-14 alkyl benzene sulphonate.<br><br>
9. A composition according to any foregoing claim wherein the anionic surfactant comprises up to 50% by weight based on the total r<br><br> weight of anionic surfactants present, of a ^14-22 mono-and/or di-alkyl phosphate ester.<br><br>
10. A composition according to claim 9 wherein said alkyl phosphate ester is present in a proportion of 2 to 40% by weight, based on the total weight of anionic surfactant present.<br><br>
11. A composition according to any foregoing claim wherein the anionic surfactant comprises from 5 to 100% by weight of a Cg-20 alkyl sulphate, based on the weight of alkyl benzene sulphonate.<br><br>
12. A composition according to claim 11 wherein the proportion by weight of alkyl sulphate is from 15 to 30% based on the weight of alkyl benzene sulphonate.<br><br>
13. A composition according to any foregoing claim wherein the anionic surfactant comprises from 5 to 150% by weight of a Cg-20 alkyl polyalkyleneoxy sulphate, based on the weight of alkyl benzene sulphonate.<br><br>
14. A composition according to claim 13 wherein the alkyl polyalkyleneoxy sulphate is a ^16-18 alkyl 1.5 to 5 mole polyethyleneoxy sulphate.<br><br>
15. A composition according to either of claims 13 and 14 wherein the proportion of alkyl polyalkyleneoxy sulphate is from 50 to 110% by weight, based on the weight of alkyl benzene sulphonate.<br><br>
16. A composition according to any foregoing claim wherein the nonionic surfactant comprises an ethoxylated alcohol.<br><br> v.<br><br> W<br><br> 2 8 NOV 199<br><br> jn|;<br><br> ft:<br><br> 224862<br><br> 17<br><br>
17. A liquid detergent composition according to any of claims 6 to 16 comprising suspended solid particles of sodium tripolyphosphate and/or zeolite.<br><br>
18. A liquid detergent composition according to any of claims 6 to 17 wherein the total proportion by weight of surfactant is from 6 to 12% by weight based on the total weight of the composition.<br><br>
19. A composition according to claim 18 comprising : water; from 4 to 10% of sodium linear Ci2-14 alkyl benzene sulphonate; from 0.5 to 4%<br><br> of a cio_i4 alkyl sulphate salt; from 0.5 to 4% of an ethoxylatedC1Q_14 alcohol having 1 to 5 mole ethyleneoxy; and frcm 20-30% sodium tripolyphosphate; all percentages being by weight based on the total weight of ■che composition.<br><br>
20. A composition according to claim 19 wherein the alkyl sulphate salt is a triethanolamine salt.<br><br>
21. A composition according to any of claims 6 to 20 additionally containing up to 2% each of sodium silicate and a sodium phospnonate and up to 1% each of soil suspending agent and optical brightener.<br><br>
22. A liquid detergent composition according to any of claims 6 to 17 having from 18 to 25% by weight of total surfactant, based on the total weight of the composition.<br><br> </p> </div>
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB878713574A GB8713574D0 (en) | 1987-06-10 | 1987-06-10 | Liquid detergent compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ224863A true NZ224863A (en) | 1992-01-29 |
Family
ID=10618686
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ224863A NZ224863A (en) | 1987-06-10 | 1988-06-01 | Surfactant system containing anionic and alkoxylated nonionic surfactants |
Country Status (26)
Country | Link |
---|---|
EP (1) | EP0295021A3 (en) |
JP (1) | JPS644700A (en) |
KR (1) | KR890000650A (en) |
CN (1) | CN88103546A (en) |
AU (1) | AU1754388A (en) |
BG (1) | BG47649A3 (en) |
BR (1) | BR8802818A (en) |
CS (1) | CS8804008A3 (en) |
DD (1) | DD270721A5 (en) |
DK (1) | DK314488A (en) |
FI (1) | FI882792A (en) |
GB (2) | GB8713574D0 (en) |
HU (1) | HUT48920A (en) |
IL (1) | IL86564A0 (en) |
IN (1) | IN172745B (en) |
IS (1) | IS3353A7 (en) |
MA (1) | MA21296A1 (en) |
NO (1) | NO882540L (en) |
NZ (1) | NZ224863A (en) |
OA (1) | OA08905A (en) |
PL (1) | PL273006A1 (en) |
PT (1) | PT87711B (en) |
TN (1) | TNSN88056A1 (en) |
ZA (1) | ZA883892B (en) |
ZM (1) | ZM3388A1 (en) |
ZW (1) | ZW7088A1 (en) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8821763D0 (en) * | 1988-09-16 | 1988-10-19 | Unilever Plc | Liquid detergents |
GB8919254D0 (en) * | 1989-08-24 | 1989-10-11 | Albright & Wilson | Liquid cleaning compositions and suspending media |
ES2066216T5 (en) * | 1989-09-13 | 1999-04-01 | Unilever Nv | LIQUID DETERGENTS. |
EP0430330A3 (en) * | 1989-11-24 | 1991-12-18 | The Procter & Gamble Company | Suspending liquid detergent compositions |
IN180345B (en) * | 1990-04-10 | 1998-01-24 | Albright & Wilson U K Ltd | |
GB2245262A (en) * | 1990-06-22 | 1992-01-02 | Unilever Plc | Aluminosilicate slurries l |
EP0482275B1 (en) * | 1990-10-22 | 1996-07-10 | The Procter & Gamble Company | Stable liquid detergent compositions containing bleach |
GB2259519B (en) * | 1991-08-30 | 1996-03-06 | Albright & Wilson | Concentrated aqueous surfactant compositions |
IN185580B (en) * | 1991-08-30 | 2001-03-03 | Albright & Wilson Uk Ltd | |
GB9217001D0 (en) * | 1992-08-11 | 1992-09-23 | Unilever Plc | Liquid compositions |
CN1037912C (en) * | 1993-03-01 | 1998-04-01 | 上海锦华科技开发公司 | Emulsive dirt detergent and its prepn. |
DE4333224A1 (en) * | 1993-09-30 | 1995-04-06 | Henkel Kgaa | Paste-shaped textile detergent |
EP0675194A1 (en) * | 1994-03-28 | 1995-10-04 | The Procter & Gamble Company | Detergent additives in structured liquids |
WO1996018713A1 (en) * | 1994-12-15 | 1996-06-20 | Albemarle Corporation | Liquid laundry detergent |
WO1998029526A1 (en) * | 1996-12-31 | 1998-07-09 | The Procter & Gamble Company | Thickened, highly aqueous, low cost liquid detergent compositions with aromatic surfactants |
US6897188B2 (en) | 2001-07-17 | 2005-05-24 | Ecolab, Inc. | Liquid conditioner and method for washing textiles |
WO2003055456A1 (en) | 2001-12-21 | 2003-07-10 | Rhodia Inc. | Stable surfactant compositions for suspending components |
US8110537B2 (en) | 2003-01-14 | 2012-02-07 | Ecolab Usa Inc. | Liquid detergent composition and methods for using |
US7682403B2 (en) | 2004-01-09 | 2010-03-23 | Ecolab Inc. | Method for treating laundry |
US20050233935A1 (en) * | 2004-04-15 | 2005-10-20 | Euen Gunn | Structured surfactant compositions |
EP2136768B1 (en) | 2007-03-23 | 2018-10-17 | Solvay USA Inc. | Structured surfactant compositions |
AU2015335977B2 (en) * | 2014-10-22 | 2019-05-30 | Rohm And Haas Company | Liquid laundry detergent containing amine additives |
JP6959370B2 (en) | 2017-06-22 | 2021-11-02 | エコラボ ユーエスエー インコーポレイティド | Bleaching with peroxyformic acid and oxygen catalyst |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL297876A (en) * | 1963-10-21 | |||
NO121968C (en) * | 1966-06-23 | 1977-06-13 | Mo Och Domsjoe Ab | |
GB1431271A (en) * | 1972-04-24 | 1976-04-07 | Unilever Ltd | Detergent compositions |
PH14451A (en) * | 1972-10-31 | 1981-07-23 | Procter & Gamble | Detergent compositions |
GB1495146A (en) * | 1974-04-11 | 1977-12-14 | Procter & Gamble | Controlled sudsing detergent compositions |
GB1562801A (en) * | 1976-01-02 | 1980-03-19 | Procter & Gamble | Liquid detergent composition |
GB2022125B (en) * | 1978-03-02 | 1982-07-07 | Albright & Wilson | Concentrated aqueous surfactant compositions |
JPS577162A (en) * | 1980-06-17 | 1982-01-14 | Toshiba Corp | Nonvolatile semiconductor memory and manufacture therefor |
US4530780A (en) * | 1981-11-16 | 1985-07-23 | Lever Brothers Company | Liquid detergent composition containing stabilizing electrolyte mixtures |
IS1740B (en) * | 1982-02-05 | 1999-12-31 | Albright & Wilson Uk Limited | Composition of cleaning liquid |
NZ205345A (en) * | 1982-08-27 | 1985-08-30 | Unilever Plc | Aqueous,built liquid detergent compositions |
MX167884B (en) * | 1983-12-22 | 1993-04-20 | Albright & Wilson | LIQUID DETERGENT COMPOSITION |
JPS61163660A (en) * | 1985-01-14 | 1986-07-24 | Seiko Epson Corp | Semiconductor memory element |
JPS61206231A (en) * | 1985-03-08 | 1986-09-12 | Mitsubishi Electric Corp | Manufacture of semiconductor device |
CA1315635C (en) * | 1986-11-14 | 1993-04-06 | Ronald L. Jacobsen | Stable liquid detergent compositions |
-
1987
- 1987-06-10 GB GB878713574A patent/GB8713574D0/en active Pending
-
1988
- 1988-05-31 IL IL86564A patent/IL86564A0/en unknown
- 1988-05-31 IS IS3353A patent/IS3353A7/en unknown
- 1988-06-01 ZA ZA883892A patent/ZA883892B/en unknown
- 1988-06-01 NZ NZ224863A patent/NZ224863A/en unknown
- 1988-06-03 EP EP19880305114 patent/EP0295021A3/en not_active Withdrawn
- 1988-06-03 GB GB08813132A patent/GB2205852A/en not_active Withdrawn
- 1988-06-03 ZW ZW70/88A patent/ZW7088A1/en unknown
- 1988-06-08 TN TNTNSN88056A patent/TNSN88056A1/en unknown
- 1988-06-08 MA MA21538A patent/MA21296A1/en unknown
- 1988-06-09 ZM ZM33/88A patent/ZM3388A1/en unknown
- 1988-06-09 HU HU882995A patent/HUT48920A/en unknown
- 1988-06-09 AU AU17543/88A patent/AU1754388A/en not_active Abandoned
- 1988-06-09 PT PT87711A patent/PT87711B/en not_active IP Right Cessation
- 1988-06-09 DK DK314488A patent/DK314488A/en not_active Application Discontinuation
- 1988-06-09 CS CS884008A patent/CS8804008A3/en unknown
- 1988-06-09 BR BR8802818A patent/BR8802818A/en not_active Application Discontinuation
- 1988-06-09 NO NO882540A patent/NO882540L/en unknown
- 1988-06-10 JP JP63141888A patent/JPS644700A/en active Pending
- 1988-06-10 DD DD88316653A patent/DD270721A5/en not_active IP Right Cessation
- 1988-06-10 BG BG84441A patent/BG47649A3/en unknown
- 1988-06-10 PL PL27300688A patent/PL273006A1/en unknown
- 1988-06-10 FI FI882792A patent/FI882792A/en not_active IP Right Cessation
- 1988-06-10 OA OA59412A patent/OA08905A/en unknown
- 1988-06-10 CN CN198888103546A patent/CN88103546A/en active Pending
- 1988-06-10 KR KR1019880007003A patent/KR890000650A/en not_active Application Discontinuation
- 1988-06-30 IN IN469DE1988 patent/IN172745B/en unknown
Also Published As
Publication number | Publication date |
---|---|
HUT48920A (en) | 1989-07-28 |
DK314488A (en) | 1988-12-11 |
CS275072B2 (en) | 1992-01-15 |
PL273006A1 (en) | 1989-04-03 |
DK314488D0 (en) | 1988-06-09 |
GB8813132D0 (en) | 1988-07-06 |
ZW7088A1 (en) | 1988-07-27 |
FI882792A0 (en) | 1988-06-10 |
IS3353A7 (en) | 1988-12-11 |
NO882540L (en) | 1988-12-12 |
ZA883892B (en) | 1989-02-22 |
AU1754388A (en) | 1988-12-15 |
OA08905A (en) | 1989-10-31 |
IL86564A0 (en) | 1988-11-15 |
EP0295021A2 (en) | 1988-12-14 |
EP0295021A3 (en) | 1991-06-19 |
TNSN88056A1 (en) | 1990-07-10 |
MA21296A1 (en) | 1988-12-31 |
GB2205852A (en) | 1988-12-21 |
ZM3388A1 (en) | 1989-02-27 |
CN88103546A (en) | 1988-12-28 |
JPS644700A (en) | 1989-01-09 |
NO882540D0 (en) | 1988-06-09 |
FI882792A (en) | 1988-12-11 |
GB8713574D0 (en) | 1987-07-15 |
BR8802818A (en) | 1989-01-03 |
CS8804008A3 (en) | 1992-01-15 |
DD270721A5 (en) | 1989-08-09 |
PT87711B (en) | 1992-10-30 |
KR890000650A (en) | 1989-03-16 |
IN172745B (en) | 1993-11-20 |
BG47649A3 (en) | 1990-08-15 |
PT87711A (en) | 1988-07-01 |
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