AU611292B2 - Detergent composition - Google Patents

Detergent composition Download PDF

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AU611292B2
AU611292B2 AU34758/89A AU3475889A AU611292B2 AU 611292 B2 AU611292 B2 AU 611292B2 AU 34758/89 A AU34758/89 A AU 34758/89A AU 3475889 A AU3475889 A AU 3475889A AU 611292 B2 AU611292 B2 AU 611292B2
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Prior art keywords
alkyl
chains
composition according
alkyl sulphate
surfactant
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AU3475889A (en
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Dennis Giles
Michael Hull
Reginald Vear Scowen
Bryan Cecil Smith
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Unilever PLC
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Unilever PLC
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/83Mixtures of non-ionic with anionic compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • C11D1/146Sulfuric acid esters
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/37Mixtures of compounds all of which are anionic
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

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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)
  • Detergent Compositions (AREA)

Description

3 11111=== :11111~: 11111~ 1 I111= III!1= 41, -i II~**IIIIL LCL- CPL~Y-- ~IC---C-CI- 'i: AUSTRALIA 1129Form Form PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE Short Title: Int. Cl: Application Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: S Priority: S Related Art: TO BE COMPLETED BY APPLICANT S 9 Name of Applicant: Address of Applicant: UNILEVER PLC UNILEVER HOUSE
BLACKFRIARS
LONDON EC4
ENGLAND
I 4 Actual Inventor: Address for Service: GRIFFITH HACK CO., 601 St. Kilda Road, Melbourne, Victoria 3004, Australia.
Complete Specification for the invention entitled: DETERGENT COMPOSITION The following statement is a full description of this invention including the best method of performing it known to me:u il C I- 14 V "v o o00 0 4 o o oJO 0 00 000 0 0 oc c 0 1 DETERGENT COMPOSITION 0 0 00 0 0C0 0' 00 0 0 0 0 S 0 0000 09 0 This invention relates to a detergent composition, in particular to a detergent composition for washing fabrics.
Fabric washing compositions contain, as an essential ingredient, surfactant system whose role is to assist in 5 the removal of soil from the fabric and its suspension in the wash liquor. Suitable detergent active materials fall into a number of classes, including anionic, nonionic and cationic materials and marketed products contain materials selected from one or more of these classes.
.O The most widely used anionic detergent active materials are the alkyl benzene sulphonates and these provide satisfactory results especially at high temperatures. There has been a desire to find alternative i t
I
c; I:r i: b i i ii 1 1 i i i; i..il 67 2 anionic surfactants for use in circumstances when alkyl benzene sulphonates are undesirable, but generally speaking the performance of other anionic detergent active materials is unsatisfactory.
Among such alternative anionic surfactants are the primary alcohol sulphates (PAS) otherwise known as alkyl sulphates. The PAS derived from tallow fat has been recommended for use. Thus, GB 1399966 (The Procter Gamble Company) discloses a detergent composition in which the surfactant system is a mixture of sodium tallow alkyl sulphate and a nonionic detergent active material. However, o otallow PAS suffers from the disadvantage that its O00 performance at low temperatures is poor. With the trend 00oo towards lower wash temperatures this becomes a serious oo 0 o0a 15 disadvantage.
00o00 oa oo 0o ,Other PAS's have been proposed in the art. Thus, for example, GB 1399966 referred to above, also discloses the 000 possibility of using the PAS derived from coconut oil. We oo have appreciated that under some circumstances coconut PAS 00 20 can perform better than tallow PAS at low temperatures, but under such circumstances its performance at higher 400 0 0000 temperatures is significantly poorer than the tallow derived material. Thus, while the consumer expects a single product 0,0 to perform satisfactorily both at high and low temperatures, the replacement of tallow PAS by coconut PAS is not an attractive option.
An objective of the present invention is to provide a surfactant system based on PAS and which is able to give a good combination of performance levels at a range of temperatures. b We have found that this can be achieved with a PAS which has a wider spread of alkyl chain lengths than -s the case when either tallow alone or coconut alone is the source of the alkyl chains. Use of a PA5 derived from a mixture of L A 3sources can perform better than tallow PAS at low temperatures and better than coconut PAS at higher temperatures. Under some circumstances there is better performance than with either tallow or coconut PAS. Even though these may give better performance at certain temperatures, use of PAS with a wider spread of alkyl chain lengths can give good performance over a wider temperature range.
The spread of chain lengths may be characterised by the presence of alkyl chains of twelve and eighteen carbon o0 0 atoms in amounts or a ratio which does not occur when the 0° alkyl chains come from a single natural source.
00o Thus, according to a first aspect of this invention 0000 there is provided a detergent composition for washing 0000 0. ^15 fabrics, the composition containing a surfactant system 0 comprising an anionic surfactant the major ingredient of which is alkyl sulphate of mixed alkyl chain length such that at least 10% by weight of the alkyl chains present in o the alkyl sulphate are C 12 chains, at least 20% by weight o oo20 of said alkyl chains are C 8 chains and the weight ratio o 9 o o of C 12 alkyl chains to C18 alkyl chains is in the range 9:4 to 1:6, preferably 2:1 to For comparison in a coconut feedstock the percentages of C12and C18 alkyl are typically 53% and 12%, amounting to a ratio over 3:1 (and indeed over 4:1) while in a tallow feedstock the alkyl chains can be 70% C 18 0 alkyl with C12 almost entirely absent.
12 In compositions of the invention, preferably at least 15% by weight of the alkyl chains present in the alkyl sulphate are C 12 while the C 18 alkyl chains are at least 25% by weight of the alkyl chains in the alkyl sulphate.
As stated, the alkyl sulphate of mixed chain lengths is the major ingredient of the anionic surfactant present, and hence over 50% of it. Of course the alkyl sulphate I' Rq; 1 t4V5 t
K^LOY$
I- i; o on 0 01 o 0o cooo o 00 0 0000 0000 o o0 o0 0 0000 0 00 00 a 0 0 o 00 00 0 0 00 0 00 0 0 0 .0 0 1 o o may constitute the whole of the anionic surfactant present.
Preferred is that the alkyl sulphate is at least 60% or even at least 80% of the anionic surfactant present.
Alkyl sulphates are also known as sulphated fatty alcohol salts. The alkyl sulphates, which are particularly envisaged for this invention, are normally produced from natural alcohols, such as those produced by reducing the glycerides of naturally occurring fats and oils.
Natural alcohols rich in C 12 alkyl chains include those derived from babassu, coconut, ouri-coury and palm kernel while alcohols rich in C 18 chains include those derived from beef tallow, kapok, olive, peanut, sesame, tall oil and teaseed.
Natural alcohols may be hardened, in which case 15 unsaturated alkyl chains will be absent. However PAS from unhardened materials, such as unhardened tallow alcohol, may be employed so that unsaturated chains are present. C,, unsaturated chains will normally be oleyl but further unsaturation may be present e.g. linoleic chains may be 20 present.
In addition to the C 12 and C 18 chains in the PAS materials useful in the present invention, other alkyl and unsaturated chains may be present. These chains will normally have between 8 and 18 carbon atoms. Materials which contain more than a small amount, i.e. more than about of chains containing more than 18 carbon atoms or less than 8 carbon atoms are less preferred.
From the point of view of ready availability, it is preferred to use a PAS derived from a mixture of tallow and coconut in the weight ratio of from 3:1 to 1:3, most preferably from 2:1 to 1:2.
It is preferred to use the water-soluble salts of i Y
I
these anionic surfactants, specifically the alkali metal (sodium or potassium) salts thereof.
Preferred compositions according to the invention include from 2% to 50%, such as from 4% to 30% by weight of the surfactant system.
The compositions of the invention also preferably contain a nonionic surfactant. We have found it to be of advantage if such a nonionic surfactant has an HLB of less than 10.5, although there is benefit even if the nonionic surfactant has an HLB greater than this.
o oo 0 00 Soo Suitable nonionic surfactants which may be used are 000 a o0 the reaction products of compounds having a hydrophobic 0 04 group and a reactive hydrogen atom, for example aliphatic 0 alcohols, acids, amides or alkyl phenols with alkylene 00 0a S 15 oxides, especially ethylene oxide either alone or with propylene oxide. Specific nonionic detergent compounds are a4, alkyl (C 6
C
22 phenols-ethylene oxide condensates, the a0 0 condensation products of aliphatic (C 8
C
18 primary or 4" secondary linear or branched alcohols with ethylene oxide, 0 20 and products made by condensation of ethylene oxide with the reaction products of propylene oxide and ethylenediamine.
a When alkylene oxide adducts of fatty materials are used as the nonionic surfactants, the number of alkylene a oxide groups per molecule has a considerable effect upon the HLB of the nonionic surfactant. The chain length and nature of the fatty material is also influential, and thus the preferred number of alkylene oxide groups per molecule depends upon the nature and chain length of the fatty material.
We have found it of advantage that the weight ratio between the anionic surfactant and the nonionic surfactant lies between 10:1 and 1:4, most preferably between 4:1 and 1:2.
I T; NOMMOMMOM rr~ 6 The surfactant system may include other surfactant materials in addition to the specified alkyl sulphate and the above mentioned nonionic materials. These other surfactant materials may be selected from other anionic detergent active materials, zwitterionic or amphoteric detergent active materials or mixtures thereof.
The level of any such further surfactant materials will not exceed 50% of the composition. It is preferably not more than 40% of the total amount of surfactant in the composition, and may perhaps be not over 5% by weight of the o 00 whole composition.
o 0o o 00 0 0 0 oo The other anionic detergent active materials which may 00 o be present may be the usual water-soluble alkali metal salts 000 .oo0 of organic sulphonates having alkyl radicals containing from 00 00 0 °0 15 about 8 to about 22 carbon atoms, the term alkyl being used to include the alkyl portion of higher acyl radicals.
Examples of suitable synthetic anionic detergent compounds o° are sodium and potassium alkyl (C 9
C
20 benzene 0 4 sulphonates, particularly sodium linear secondary alkyl (C 0
C
1 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 monoglyceride sulphates and sulphonates; sodium and potassium salts of sulphuric acid esters of higher (C 8 to Cz fatty alcohol-ethylene oxide reaction products; the reaction products of fatty acids such as coconut fatty acids esterified with isethionic acid and neutralised with sodium hydroxide; sodium and potassium salts of fatty acid amides of methyl taurine; alkane monosulphonates such as those derived by reacting alpha-olefins (C 8
-C
20 with sodium bisulphite and those derived from reacting paraffins with
SO
2 and Cl 2 and then hydrolysing with a base to produce a random sulphate. A further anionic detergent active which may be included is soap, especially soap with a high p 7 proportion of unsaturated acyl chains.
The compositions of the invention may contain a detergency builder material, this may be any material capable of reducing the level of free calcium ions in the wash liquor and will preferably provide the compositions with other beneficial properties such as the generation of an alkaline pH and the suspension of soil removed from the fabric. The amount of builder material in a composition of this invention may in particular be from 15% to 60% by weight of the composition.
o Examples of phosphorus-containing inorganic detergency o o builders, when present, include the water-soluble salts, 00o 0 o especially alkali metal pyrophosphates, orthophosphates, 0 000 metaphosphates, polyphosphates and phosphonates. Specific 0 0 15 examples of inorganic phosphate builders include sodium and 00 00 0 CT G S° potassium tripolyphosphates, orthophosphates and hexametaphosphatez;.
0000 0 0 0 00 a Examples of non-phosphorus-containing inorganic o 00 o oo detergency builders, when present, include water-soluble 0 o0 20 alkali metal carbonates, bicarbonates, silicates and D 0 0 0 crystalline and amorphous aluminosilicates. Specific examples include sodium carbonate (with or without calcite o seeds), potassium carbonate (with or without calcite seeds), S0 sodium and potassium bicarbonates and silicates.
s Examples of organic detergency builders, when present, include the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates, polyacetyl carboxylates and polyhydroxysulphonates. Specific examples include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, melitic acid, benzene polycarboxylic acids and citric acid.
It is preferred that the compositions according to the 1 1 I i_ 8 invention be alkaline, that is at the concentra-.on of 1 g/l in distilled water at 25°C the pH should be at least 8, preferably at least 10. To this end the compositions may include a water-soluble alkaline salt. This salt may be a detergency builder or a non-building alkaline material.
Apart from the ingredients already mentioned, a number of optional ingredients may also be present.
Examples of other ingredients which may be present in the composition include fabric softening agents such as fatty amines, fabric softening clay materials, lather So° o boosters such as alkanolamides, particularly the 0 o°°o monoethanolamides derived from palm kernel fatty acids and 0oo O oo coconut fatty acids, lather depressants, oxygen-releasing O 0 00o bleaching agents such as sodium perborate and sodium o .00 15 percarbonate, peracid bleach precursors, chlorine-releasing 00 00 0 o bleaching agents such as trichloroisocyanuric acid, inorganic salts such as sodium sulphate, and, usually 0oO present in very minor amounts, fluorescent agents, perfumes including deodorant perfumes, enzymes such as proteases, 0 00 0 20 cellulases, amylases and lipase, germicides and colourants.
0 00 0 0 0 aThe detergent compositions according to the invention may be prepared by a number of different methods according to their physical form. In the case of granular products S they may be prepared by dry-mixing or coagglomeration. A 4(400 preferred physical form is a granule incorporating a detergency builder salt and this is most conveniently manufactured by spray-drying at least part of the composition. In this process a slurry is prepared containing the heat-insensitive components of the composition such as the surfactant system, builder material and filler salt. The slurry is spray-dried to form base powder granules with which any solid heat-sensitive ingredients may be mixed, such ingredients including bleaches and enzymes. The specified nonionic surfactants can be liquified by melting or solvent dissolution and q i 1 i' i i 1 1
I~
o sprayed onto the base powder granules, rather than including them in the slurry for spray-drying. The invention will now be described in more detail in the following non-limiting examples.
EXAMPLES 1 TO 6 Wash liquors were prepared in water having a hardness of 250 FH (equivalent to a free calcium ion concentration of x 10- 3 molar). The wash liquor contained the equivalent of 6 g/l of a composition containing (by weight): 0 0o 10 Specified anionic surfactant 9% o o Specified nonionic surfactant 4% 000 a 00 Sodium tripolyphosphate 23% 0 0 0 Sodium carbonate 6% 0000 0o00 Sodium alkaline silicate 00 00 o 15 Sodium sulphate 30.8% Sodium chloride 2.93% 000 Water balance a O 9 0 00 o 00 The sodium chloride was included as being equivalent a in ionic strength to 5% sodium perborate monohydrate which 20 would be present in practice. The bleach is left out of these experiments in order to avoid confusion between a detergency and bleaching effect in the interpretation of the S results.
I t The wash liquors were used to wash a fabric load at liquor to cloth ratio of 50:1. The load included a number of polyester monitors to which had previously been applied an amount of C 14 tagged triolein. Measurement of the level of tagged triolein after washing, using standard radiotracer techniques, gives an indication of the degree of detergency, i.e. soil removal, obtained.
The wash time was 20 minutes with an agitation of rpm. Washes were isothermal at temperatures as specified I i below.
f The anionic surfactants used were as set out in the following table: Chain Length Distribution <C 8 C1 C 18 <Cis Surf actant Origin ELFAN 2801 ELFAN KT5501 SUL.FOPON T55 2 Coconut Coco/tallow mix Tallow 0 00 00 a 0 00 00 0 00 0 0 0 009 00.0.
0- 00 0000 0 0 0 00007 0 00 00 a 000 C0 0 090 0 0 10 1- ex Akzo 2 ex Henkel In Examples 1 to 6 the nonionic surfactant was SYNPERONIC A7 (ex ICI) which is principally C 1 3 /Cl. alcohol ethoxylated with an average of 7 moles of ethylene oxide.
This nonionic surf actant has an HLB of 11.7.
The results obtained were as follows: 00 0 0 00 000.000 0 0 Example No 1 2 3 4 6 Anionic ELFAN 280 ELFAN KT550 SULFOPON T55 ELFAN 280 ELFAN KT550 SULFOPON T55 Wash Temperaturem 30 0
C
300 C 300 C 60 0
C
60 0
C
600 C Soil Removal 24.9 30.0 24.9 30.5 36,3 46.7 From these results it is apparent that at 60 0 C ELFAN KT550 outperforms the coconut only derived PAS, ELFAN 280.
At the lower temperature of 30 0 C, ELFAN KT550 outperforms both the coconut only and the tallow derived materials.
it i EXAMPLES 7 TO 12 Examples 1 to 6 were repeated, except that the nonionic surfactant was a mixture of 1 part SYNPERONIC A7 with 3 parts of SYNPERONIC A3, which is a similar material in which the alcohol is ethoxylated with an average of 3 moles ethylene oxide per molecule. This nonionic surfactant mixture has an HLB of approximately The results were as follows: 0 01 0 00 o on 00 4 0 o0 00 0o 0 0 0 a ooo o 000 0000 00 00 00 0 o a 0o 4 S4 t SI 1 0 0 tt 0:000 0 0 Example No 7 8 9 10 15 11 12 Anionic ELFAN 280 ELFAN KT550 SULFOPON T55 ELFAN 280 ELFAN KT550 SULFOPON T55 Wash Temperature 30°C 30°C 30°C 60°C 60°C 600C Soil Removal 39.0 38.7 30.4 44.6 49.8 54.4
I)
From these results it is apparent, as with Examples 1 to 6, that at 60°C ELFAN KT550 outperforms the coconut only derived PAS, ELFAN 280. At the lower temperature, ELFAN KT550 outperforms the tallow only derived PAS, SULFOPON while not being significantly different in performance to the coconut only derived material.
A comparison of the results in Examples 7 to 12 with those in Examples 1 to 6 demonstrates the preference for utilising a nonionic surfactant with a lower HLB.
EXAMPLES 13 TO 24 Examples 1 to 3 were repeated but the levels and proportions of the surfactants were varied. The variations in composition and the results are set out in the list below in which "A3" and "A7" denote SYNPERONIC A3 and SYNPERONIC A7. The wash temperature was 30°C in each instance, as with Examples 1 to 3.
II h i Pt I- I r LII_~ Example No 13 14 16 17 18 19 21 22 23 24 Anionic 12% ELFAN 280 12% ELFAN KT550 12% SULFOPON T55 9% ELFAN 280 9% ELFAN KT550 9% SULFOPON T55 9% ELFAN 280 9% ELFAN KT550 9% SULFOPON T55 9% ELFAN 280 9% ELFAN KT550 9% SULFOPON T55 Nonionic 1.33% A7 1.33% A7 1.33% A7 2% A7 2% A7 2% A7 3% A7 3% A7 3% A7 4% A7 4% A7 4% A7 4% A3 4% A3 4% A3 A3 A3 A3 A3 A3 A3 A3 A3 A3 Soil Removal 42.9 43.7 34.5 37.3 36.8 32.3 35.2 37.2 33.0 34.3 36.1 33.2 o o 0 04 0 0 0 0 00 o oo 0 0 0 0 o o 0 00 oo a 0o o oo o o o 00o 00 0 0Q 0 0 00 o oo 0 00 0 0 0 040 0 Od 0 0 0 0 0 000000 4 a It will be seen that in every case, the ELFAN KT550 outperformed the all tallow SULFOPON T55 and came close to or surpassed the all coconut ELFAN 280. In every case, this amounts to a soil removal which is better than the average of the figures for the all coconut and all tallow derived materials.
EXAMPLES 25 TO 31 Wash liquors were prepared in water of 30 0
FH
(equivalent to a free calcium ion concentration of 3.0 x 10 3 molar). The wash liquor contained the equivalent of 6g/l of a composition containing (by weight): Specified surfactant Zeolite Polyacrylate Sodium sulphate Sodium carbonate Water 13% 24% 20.6% 12% balance Each wash liquor composition was employed to launder 13 several test cloths in a Tergotometer, in a heat-up cycle to After laundering the increase in reflectance of the test cloths was measured.
The test cloths employed had various stains as follows: EMPA-104 Stain of Indian ink and olive oil.
Stain predominantly wool fat, with minor amounts of kaolin, carbon black and iron oxide.
PC-9 Stain of ground nut oil, Indian ink and iron oxide.
1 0 8 1 00 The specified surfactant(s) consisted of some or all 000 8 o. of hardened tallow alcohol sulphate (TAS) and/or coconut alcohol sulphate (CAS) and mixtures with nonionic surfactant (NI) which was SYNPERONIC A3, i.e. C /Cis fatty alcohol Sa0 15 ethoxylated with an average of 3 moles of ethylene oxide per molecule.
o 0 0 Results were as follows: 0 0 0 o 0 'Example No Surfactant(s) Increase in Reflectance PC-9 EMPA-104 100% TAS 0% CAS 17.1 18.9 21.5 26 60% TAS 40% CAS 21.8 19.3 24.3 27 40% TAS 60% CAS 23.7 19.7 22.2 28 0% TAS 100% CAS 18.4 17.9 20.6 29 20% NI 80% TAS 0% CAS 20.0 19.8 17.9 20% NI 40% TAS 40% CAS 24.6 21.0 20.3 31 20% NI 0% TAS 80% CAS 19.2 18.9 16.9 It will be seen that in each case the mixture of hardened tallow based and coconut based surfactants gave better detergency than either of them used alone.
14 EXAMPLES 32 AND 33 Wash liquors were prepared in water having a hardness of 25" FH. The wash liquors contained the equivalent of 6 g/l of a composition containing (by weight): Ingredient by weight o #0 a o o o o o o o o 0o00 00 00 0 o oo 4 0O 0 D0 4 t It C1 11(t Specified anionic SYNPERONIC A7 SYNPERONIC A3 Zeolite Sodium sulphate Sodium carbonate Sodium silicate Sodium chloride Moisture 9 1 3 26.6 19.5 14.0 1.3 balance to 100% For Example 32 the anionic surfactant was ELFAN KT550.
For Example 33 the anionic surfactant was PAS derived from myristyl alcohol C 14 alcohol). The wash liquors were tested as in Examples 1 to 6, although a different grade of polyester was used for the test cloths.
Soil removal results were: Example 32 (ELFAN KT550) Example 33 (C 14
PAS)
28.1% 26.0% EXAMPLE 34 The following formulation was prepared by spray drying a slurry of some of the ingredients to form a base powder and then subsequently spraying on some of the nonionic surfactant and post dosing the remaining ingredients.
1- Ingredients Base powder Anionic (see below) SYNPERONIC A7 Zeolite Sodium sulphate Sodium carbonate Moisture and miscellaneous Spray-on SYNPERONIC AS Post-dose Sodium silicate Sodium perborate ionohydrate SYNPERONIC A3 15 TAED granules Anti foam Enzyme Perfume Sodium carbonate Parts by weight 26.6 19.5 13.7 71.8 1.0 1.3 2.8 0.6 0.3 12.0 30.0 0 0 00 0 00 o ,4 O 0 000 0 00 00 0 004 0000 0000 00 00 0 0 0 o 0 0 00 00 ~3 o oo 00 0 0 .0 0 Qo 00 0 000 0 20 Total 102.8 This composition was used to wash a variety of stained fabrics under a variety of conditions, results being assessed by measuring the reflectance of treated monitors.
The anionic surfactants used were tallow PAS, coconut PAS and a 50/50 mixture of the two.
The benefits observed in previous Examples were again observed in this case also. Thus the 50/50 mixture generally gave better performance than the coconut PAS alone, while on a number of stains (notably dirty motor oil, and make-up on white cotton) the mixture out-performed both alternatives.

Claims (7)

1. A detergent composition for washing fabrics, the composition containing a surfactant system comprising an anionic surfactant the major ingredient of which is an alkyl sulphate of mixed alkyl chain length such that at least by weight of the alkyl chains present in the alkyl sulphate are C 12 chains, at least 20% by weight of said alkyl chains o oo 10 are C 1 chains and the ratio of C 1 alkyl chains to C, 0 a alkyl chains is in the range 9:4 to 1:6. So o 2. A composition according to claim 1 wherein the said ooo 0 weight ratio is in the range 2:1 to 0 00 o C
3. A composition according to claim 1 or claim 2 wherein at least 15% by weight of the alkyl chains are C12 chains while at least 25% are C 1 chains. 00o 00 0 1 oooa 20 4. A detergent composition according to claim 1 in which o0 the alkyl sulphate is a mixture of tallow alkyl sulphate and g" c, coconut alkyl sulphate in a weight ratio of 3:1 to 1:3. o 0 A detergent composition according to claim 1 in which 00, 2 25 the alkyl sulphate is a mixture of tallow alkyl sulphate and 0 00 o0 0 coconut alkyl sulphate in a weight ratio of 2:1 to 1:2. 0 0Q
6. A composition according to any one of the preceding claims wherein the alkyl sulphate of mixed chain length is at least 60% of the anionic surfactant.
7. A composition according to any one of claims 1 to wherein the alkyl sulphate of mixed chain length is at least of the anionic surfactant. j
8. A detergent composition according to any one of the preceding claims which additionally contains a nonionic surfactant. S- 17
9. A detergent composition according to claim 8 in which the nonionic surfactant has an HLB of less than 10.5.
10. A detergent composition according to claim 8 or claim 9 in which the weight ratio of alkyl sulphate to nonionic surfactant is in the range 10:1 to 1:4. 0 0 0.00 000. 0 0 0.0o DATED THIS 21ST DAY OF MARCH 1991 00 UNILEVER PLC 00 By its Patent Attorneys: 00 GRIFFITH HACK CO. Fellows Institute of Patent Attorneys of Australia. 00. 00 0 0 0 00 0 00 0 0 0 0 U
AU34758/89A 1988-05-17 1989-05-12 Detergent composition Ceased AU611292B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888811672A GB8811672D0 (en) 1988-05-17 1988-05-17 Detergent composition
GB8811672 1988-05-17

Publications (2)

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AU3475889A AU3475889A (en) 1989-11-23
AU611292B2 true AU611292B2 (en) 1991-06-06

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EP (1) EP0342917B2 (en)
JP (1) JPH0813984B2 (en)
KR (1) KR960000198B1 (en)
AU (1) AU611292B2 (en)
BR (1) BR8902281A (en)
CA (1) CA1335488C (en)
DE (1) DE68929184T3 (en)
ES (1) ES2143454T5 (en)
GB (1) GB8811672D0 (en)
IN (1) IN168406B (en)
MY (1) MY105084A (en)
OA (1) OA09118A (en)
TR (1) TR23981A (en)
ZA (1) ZA893682B (en)

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KR0170424B1 (en) * 1990-07-05 1999-01-15 호르스트 헤를레,요한 글라슬 Process for making washing and cleaning active tensile granulates
DE4024657A1 (en) * 1990-08-03 1992-02-06 Henkel Kgaa METHOD FOR DRYING AND GRANULATING WAESS-RATED PASTE WASH ACTIVE AGGREGATE MIXTURES
DE4038476A1 (en) * 1990-12-03 1992-06-04 Henkel Kgaa Prepn. of solid washing compsn. - by mixing aq. alkyl sulphate paste with sodium sulphate and/or aluminosilicate and shaping or grinding
DE4241473A1 (en) * 1992-12-09 1994-06-16 Henkel Kgaa Water-soluble surfactant mixtures for liquid detergents
GB9313878D0 (en) * 1993-07-05 1993-08-18 Unilever Plc Detergent composition or component containing anionic surfactant and process for its preparation
AU7062494A (en) * 1993-07-12 1995-02-13 Procter & Gamble Company, The Surfactant system
DE4403323A1 (en) * 1993-09-23 1995-08-10 Henkel Kgaa Extruded washing or cleaning agents with improved dissolving properties
DE4415369C1 (en) * 1994-05-02 1995-08-31 Henkel Kgaa Heterogeneous surfactant granulate useful in washing powder and detergent
DE4432365A1 (en) * 1994-09-12 1996-03-14 Henkel Kgaa Anhydrous surfactant mixtures
GB2296919A (en) * 1995-01-12 1996-07-17 Procter & Gamble Detergent composition
DE19500644B4 (en) * 1995-01-12 2010-09-09 Henkel Ag & Co. Kgaa Spray-dried detergent or component thereof
CN1093876C (en) * 1996-04-16 2002-11-06 普罗格特-甘布尔公司 Liquid cleaning compsns. containing selected mid-chain branched surfactants
PH11997056158B1 (en) * 1996-04-16 2001-10-15 Procter & Gamble Mid-chain branched primary alkyl sulphates as surfactants
MA24136A1 (en) * 1996-04-16 1997-12-31 Procter & Gamble MANUFACTURE OF SURFACE AGENTS.
EG21174A (en) * 1996-04-16 2000-12-31 Procter & Gamble Surfactant manufacture
EG22088A (en) * 1996-04-16 2002-07-31 Procter & Gamble Alkoxylated sulfates
WO1998018889A2 (en) * 1996-10-30 1998-05-07 Henkel Kommanditgesellschaft Auf Aktien Anhydric surfactant mixtures
US6093856A (en) * 1996-11-26 2000-07-25 The Procter & Gamble Company Polyoxyalkylene surfactants
US6242406B1 (en) 1997-10-10 2001-06-05 The Procter & Gamble Company Mid-chain branched surfactants with cellulose derivatives
ZA989155B (en) 1997-10-10 1999-04-12 Procter & Gamble Mixed surfactant system
EP1023425A1 (en) 1997-10-14 2000-08-02 The Procter & Gamble Company Granular detergent compositions comprising mid-chain branched surfactants
CN1281500A (en) 1997-10-14 2001-01-24 普罗格特-甘布尔公司 Light-duty liquid or gel dishwashing detergent compositions comprising mid-chain branched surfactants
JP2001519376A (en) 1997-10-14 2001-10-23 ザ、プロクター、エンド、ギャンブル、カンパニー Personal cleansing composition comprising a mid-chain branched surfactant
JP5000991B2 (en) * 2006-11-28 2012-08-15 三洋化成工業株式会社 Cleaning agent for electronics materials
CA2958319A1 (en) 2014-09-08 2016-03-17 The Procter & Gamble Company Detergent compositions containing a branched surfactant
WO2016040248A2 (en) 2014-09-08 2016-03-17 The Procter & Gamble Company Detergent compositions containing a branched surfactant

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Also Published As

Publication number Publication date
AU3475889A (en) 1989-11-23
EP0342917B2 (en) 2006-10-25
EP0342917A3 (en) 1990-09-12
KR960000198B1 (en) 1996-01-03
JPH0218498A (en) 1990-01-22
EP0342917A2 (en) 1989-11-23
TR23981A (en) 1991-01-14
CA1335488C (en) 1995-05-09
OA09118A (en) 1991-10-31
ZA893682B (en) 1991-01-30
DE68929184T3 (en) 2007-02-15
KR890017348A (en) 1989-12-15
DE68929184T2 (en) 2000-08-24
DE68929184D1 (en) 2000-04-27
JPH0813984B2 (en) 1996-02-14
GB8811672D0 (en) 1988-06-22
BR8902281A (en) 1990-01-09
MY105084A (en) 1994-08-30
EP0342917B1 (en) 2000-03-22
ES2143454T3 (en) 2000-05-16
IN168406B (en) 1991-03-30
ES2143454T5 (en) 2007-06-16

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