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NZ199235A - Controlled-sudsing detergent compositions - Google Patents

Controlled-sudsing detergent compositions

Info

Publication number
NZ199235A
NZ199235A NZ199235A NZ19923581A NZ199235A NZ 199235 A NZ199235 A NZ 199235A NZ 199235 A NZ199235 A NZ 199235A NZ 19923581 A NZ19923581 A NZ 19923581A NZ 199235 A NZ199235 A NZ 199235A
Authority
NZ
New Zealand
Prior art keywords
alkyl
alkyl benzene
washing powder
suds
weight
Prior art date
Application number
NZ199235A
Inventor
G Butler
M N A Carter
M Curtis
R M Davies
Original Assignee
Unilever Plc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10518045&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NZ199235(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever Plc filed Critical Unilever Plc
Publication of NZ199235A publication Critical patent/NZ199235A/en

Links

Classifications

    • 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/36Organic compounds containing phosphorus
    • C11D3/362Phosphates or phosphites
    • 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
    • C11D1/22Sulfonic acids or sulfuric acid esters; Salts thereof derived from aromatic 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
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions

Landscapes

  • 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)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Description

New Zealand Paient Spedficaiion for Paient Number 1 99235 199235 Priority ,'ik . 17,'Jel '80 J •tB*ariaaa««a <• Coretpl®to Cpcc.'f}cation Filed: Pubiicatson Date: ,... ".0.--Jcurrial, Ko: '?.^7..
W. ^11 Ml' «gg ■ •« m a &rat k t);< No.: Date: NEW ZEALAND PATENTS ACT, 1953 j * $ V COMPLETE SPECIFICATION CONTROLLED-SUDSING DETERGENT COMPOSITIONS X/We, UNILEVER PLC a British company of Unilever House, Blackfriars, London EC4, England, hereby declare the invention for which k/ we pray that a patent may be granted to5fK«/us, and the method by which it is to be performed, to be particularly described in and by the following statement:- 1 _ (followed by page la) 19 92 - 1 o-- eC . 1070 CONTROLLED GUDGING DETERCEMG? COMPOGITIONC This invention relates to controlled suds washing powders containing alkyl benzene sulphonate as a detergent active component primarily designed for use in front loading or drum type washing machines.
Most controlled suds washing powders contain anionic surfactants usually in admixture with nonionic surfactants, and the suds generated by the surfactants is controlled by a suds suppressant, soap being the one most commonly used. However, manufacturers are beginning 10 to be willing to accept the cost penalty of using suds controllers other than soap because of the increased flexibility they give in formulation of the detergent active component. Even so, it is necessary to minimise the additional cost which use of these compounds involves.
JDB02L 2 - /m!7& eerirfrTB We have now discovered that when an alkyl benzene sulphonate is used as the anionic surfact component of the washing powder, and an alkyl phosphoric acid or a salt thereof is used as the suds controller, then very effective 5 suds control can be achieved by a selection of the type of alkyl benzene sulphonate used.
Accordingly the present invention provides a washing powder comprising 5% or more by weight of water-soluble salts of alkyl benzene sulphonates in which the total 10 content of alkyl groups containing 14 or more carbon atoms is less than 15% by weight of the alkyl benzene sulphonates, and a suds controller comprising an alkyl phosphoric acid or a salt thereof.
The alkyl benzene precursors of the sulphonates of the 15 invention may be prepared from cracked wax olefines, from polymerized lower olefines or by any other desired route, provided that they conform to the chain length and molecular weight criteria of the invention.
The characteristics of the alkyl benzene sulphonates 20 are extremely important to the present invention, since we have discovered that if sulphonates containing high proportions of alkyl groups having 14 or more carbon atoms are used, the suds produced requires significantly greater amounts of suds controller to be used in order to achieve 25 the target suds profile.
It is preferred that the total content of alkyl sulphonates having 14 or more carbon atoms is less than 5% by weight. Also preferred is that the mean molecular weight of the unsulphonated hydrocarbon is from 235 to 245. 30 The alkyl benzene sulphonates may be used in combination with other anionic detergent active species. Examples of such materials are sodium primary and secondary alkyl sulphates, sodium olefine sulphonates and sodium alkane sulphonates. Of these, the ^i2~^20 Pri-mary anc^ 35 secondary alkyl sulphates are preferred. "c Lr-6N0Vf$*84 SV923 Preferred total amounts of anionic surfactant in the compositions of the invention are from 5 to 25% by weight, most preferably 5 to 15% by weight. Desirably the selected alkyl benzene sulphonates will constitute at least half of 5 these amounts and in any event at least 5% by weight of the composition.
Nonionic surfactants may also be present in the compositions of the invention in amounts of up to 15% by weight. Preferred nonionic surfactants are the Cg-C24 10 primary and secondary aliphatic alcohols, ethoxylated with from 3 to 25 moles of ethylene oxide per mole of alcohol.
. Particularly preferred are the C1Q-C18 primary alcohol ethoxylates containing from 5 to 15 moles of ethylene oxide. We have found C^2_i5 primary alcohol 7EO 15 ethoxylate to be best from the point of view of detergency.
The second essential component of the compositions of the invention is an alkyl phosphoric acid, or a salt thereof, preferably mixed with a hydrocarbon oil or wax. The preferred alkyl phosphoric acids have the general 20 formula O Rl°(E°)n - P - OH (I) A where A is -OH or F^OCEO^-, and R2 are the same or different Ci2-C24' preferably straight or branched chain, saturated or unsaturated alkyl groups, essentially C^g-C-^g linear saturated groups, and 30 m and n are the same or different and are 0 or an integer of from 1 to 6. Preferably A is -OH and n is 0, so that the compounds are monoalkyl phosphoric acids, preferably with linear alkyl groups. These compounds may be present either as the free acid or as a sodium, potassium, calcium 35 or magnesium salt or as a mixture thereof. <fc "X J77/ The amount of the alkyl phosphoric acid or salt thereof used in the detergent compositions can be varied widely from a minimum level of about 0.05% up to a practical maximum of about 5, preferably about 0.1% to 5 about 3% by weight. Higher levels than 5% can be employed but this would be uneconomical and would generally not give any product advantages.
Suitable hydrocarbon waxes for use in the detergent compositions are water insoluble materials of either 10 synthetic, mineral, vegetable or animal origin, which are dispersible in the detergent solutions. The waxes should normally melt at a temperature between about 20°C and about 120°C, preferably not more than about 90°C and especially in the range of about 30"C to about 70°C, i.e. lower than 15 the maximum intended wash temperatures for the detergent compositions.
The preferred waxes are of mineral origin, especially those derived from petroleum, including microcrystalline and oxidised microcrystalline petroleum waxes, petroleum 20 jelly ('Vaseline') and paraffin waxes. Petroleum jelly is correctly a semi-solid wax, usually having a drop melting point of about 50°C, but is for convenience here grouped with other solid waxes. Synthetic waxes such as Fischer-Tropsch and oxidised Fischer-Tropsch waxes, or 25 Montan waxes, or natural waxes such as beeswax, candelilla and carnauba waxes may be used if desired. Any of the waxes described may be used alone or in admixture with other waxes. The waxes should be readily dispersible in the detergent liquor but not soluble therein, and 30 preferably they should not have very high saponification values, e.g. not in excess of about 100. Emulsifying or stabilising agents for the waxes can also be included in the detergent composition.
The amount of wax is normally from about 0.05% to 35 about 10%, preferably about 0.1% to about 5% and especially about 0.5% to about 3% in the composition. The total 199235 eg-; 107 8' amount of the alkyl phosphoric acid or salt and the hydrocarbon wax is generally from about 0.2% to about 20% by weight of the composition, preferably about 0.5% to about 5% by weight. The ratio of the amount of the alkyl 5 phosphoric acid or salt to the wax can be varied widely from about 1:25 to about 10:1 parts by weight but is generally from about 1:20 to about 10:1 parts by weight, preferably from about 1:10 to about 1:1 parts by weight.
In addition to the wax which may be used with the 10 alkyl phosphoric acid or salt in the detergent composition, a hydrocarbon oil may also be present, either added separately or jointly with the wax, for example in order to facilitate addition of the wax or to modify its melting point or dispersion characteristics.
Examples of suitable liquid hydrocarbons are mineral, vegetable or animal oils of which colourless mineral oils are preferred. Either light or heavy mineral oil or mixtures thereof may be employed, but of course any liquid hydrocarbon used must be of low volatility at normal fabric 20 washing temperatures. Other oils which could be used if desired are vegetable oils such as sesame oil, cottonseed oil, corn oil, sweet almond oil, olive oil, wheat germ oil, rice bran oil, or peanut oil, or animal oils such as lanolin, neat's foot oil, bone oil, sperm oil or cod liver 25 oil. Any such oils used should of course not be highly coloured, of strong odour or otherwise unacceptable for use in a detergent composition.
Other suds controllers may also be used in combination with the alkyl phosphoric acid-based suds controllers. 30 Examples of these are silicone-based controllers, for example particles of granular sodium tripolyphosphate impregnated with organopolysiloxane and encapsulated in wax, or hydrophobic silica particles impregnated with an organopolysiloxane. Another example, which is of 35 particular interest, is a particle having a spherical or cylindrical core, desirably of sucrose, coated with an 15J235 absorbent such as titanium dioxide which is impregnated with polysiloxane, the whole particle being coated with wax. Mixtures of poiysiloxanes and waxes or ethylene distearimides either alone or in admixture with waxes can 5 also be used as auxiliary suds controllers.
A detergency builder will normally be included within the compositions of the invention. Several suitable detergency builders are well-known and commercially available, examples being alkali metal, ortho-, pyro- and 10 tripolyphosphates, alkali metal carbonates and bicarbonates, alkali metal polyphosphonates, alkali metal nitrilotriacetates and the host of organic builders which have been suggested as a response to the anti-phosphate lobby, examples of which are sodium carboxymethyloxy-15 succinate, sodium citrate, and sodium polyacrylate.
Other detergency builders are the sodium carbonate/ finely divided calcite combination, and the crystalline or amorphous aluminosilicate cation exchange materials. These builders may be used in an amount of from 5 to 80% by 20 weight of the composition, preferably 10 to 60% by weight.
The compositions of the invention may also contain oxygen bleaches such as sodium perborate and sodium percarbonate, fillers such as sodium sulphate, and moisture and minor components such as slurry hydrotropes, corrosion 25 inhibitors, anti-redeposition agents, anti-ashing agents, anti-oxidants, fluorescers and optical brighteners, enzymes, blue-whiteners and pigments and dyestuffs.
The invention will be further illustrated by the following Examples. 19i92 w C • 1^1 iypwiu Example 1 A series of spray-dried powders was produced to the following general formulation and by the following general method: Parts by Weight Sodium alkylbenzene sulphonate 8.0 Primary C12-15 alcohol ethoxylate 7EO 3.0 Sodium silicate 8.0 Sodium tripolyphosphate 35.0 Sodium sulphate 7.0 Sodium carboxymethylcellulose 1.0 Moisture, fluorescers and stabilisers 14.0 A suds suppressant in the form of a mixture of one part of alkyl phosphoric acid ester with three parts of petroleum jelly was sprayed onto this powder as it fell in a cascade from one conveyor belt to another. 24 parts of sodium perborate tetrahydrate were then mixed with the 20 spray-dried powder, together with perfume.
The suds produced by each powder, varying one from the other as shown below, were assessed as follows: 2\ kg loads of white terry cotton towelling were washed in Hoover (registered trade mark) front-loading 25 automatic washing machines using water of 26°H hardness and 200 g of powder. The washing programme used washes at 90 °C.
The suds height of each wash liquor was measured using an arbitrary scale attached to the window of the machines. 30 Each suds assessment was performed four times, the average suds height being quoted in the following tables, which are interpolations from a graph. The graph was produced directly from the results in the experiments.
In the first series of experiments, three sets of 35 powder were used, Set A, the control set, containing a sulphonate of an alkyl benzene having a molecular weight of f9^235 255 and Sets B and C, the sets in accordance with the invention, containing a sulphonate of an alkyl benzene having a molecular weight of 241 and 242 respectively. The actual alkyl chain length distribution is shown in 5 Table 1.
Five variants of each set of powder were prepared by spraying the powder with 0.6, 0.8, 1.0, 1.2 and 1.4% by weight respectively of the alkyl phosphoric acid/petroleum jelly mixture and the suds height was assessed as 10 described. The results are shown in Table 2.
It can be seen that whereas Powder A containing an alkyl benzene sulphonate having substantial proportions of C14' C15 an^ C16 groups in the composition produces over-foaming at the lower levels of suds-15 suppressant, the powders in accordance with the invention do not, and indeed produce only a trace of suds at the higher levels of suppressant.
Table 1 Allcyl chain length djotrlbutlon of the various allcyl benzene sulphonates (AJ3S) Allcyl chain length C C11 °12 0 11 Cl/l ^15 °16 Mean Molecular ADS Weight - A B C 255 241 242 8 9 10 33 37 ,,..32 33 19 19 ll trace nil trace nil i vn I (3

Claims (7)

Table 2 Maximum Suda llelp.bt Produced by 5 Variants of 3 Powders Sudo Suppressant (%) ABS Mean Molecular Weight A 255 0.6 over-foam 0.8 over-foam 1.0 21 1.2 16 1.4 12 0 1 B 241 242 19 15 13 8 5 7 trace trace WHAT+/WE CLAIM IS: CLAIMS - 11 -
1. A washing powder comprising 5% or more by weight of water soluble salts of alkyl benzene sulphonates and a suds controller comprising an alkyl phosphoric acid or a salt thereof, characterised in that the total content of alkyl groups containing 14 or more carbon atoms in the alkyl benzene sulphonates is less than 15% by weight of the alkyl benzene sulphonates.
2. A washing powder according to claim 1 characterised in that the total content of alkyl groups containing 14 or more carbon atoms is less than 5% by weight of the alkyl benzene sulphonates.
3. A washing powder according to claim 1 or claim 2 characterised in that the average molecular weight of the alkyl benzene from which the alkyl benzene sulphonate is prepared is 235 to 245.
4. A washing powder according to any one of the preceding claims characterised in that the alkyl benzene sulphohate is combined with a Cg-C24 Primary or secondary aliphatic alcohol ethoxylated with from 3 to 25 moles of ethylene oxide per mole of alcohol.
5. A washing powder according to claim 4 characterised in that the ethoxylated alcohol is a ^i2~C15 Primary alcohol ethoxylated with from 5 to 10 moles of ethylene oxide per mole of alcohol.
6. A washing powder according to any one of the preceding claims characterised that the suds controller comprises an alkyl phosphoric acid or a salt thereof, in combination with a hydrocarbon oil or wax. itT923
7. A washing powder comprising an alkyl benzene sulphonate and an alkyl phosphoric acid suds controller, substantially as herein before described in compositions B and C of the Example. dated this (& day of *81 A. J. PARK & SON per agents for the applicants
NZ199235A 1980-12-17 1981-12-10 Controlled-sudsing detergent compositions NZ199235A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB8040446 1980-12-17

Publications (1)

Publication Number Publication Date
NZ199235A true NZ199235A (en) 1985-02-28

Family

ID=10518045

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ199235A NZ199235A (en) 1980-12-17 1981-12-10 Controlled-sudsing detergent compositions

Country Status (13)

Country Link
EP (1) EP0054436B2 (en)
JP (1) JPS57125299A (en)
AR (1) AR225124A1 (en)
AT (1) ATE7928T1 (en)
AU (1) AU549669B2 (en)
BR (1) BR8108146A (en)
CA (1) CA1163522A (en)
DE (1) DE3164235D1 (en)
DK (1) DK558981A (en)
FI (1) FI67400C (en)
NO (1) NO814304L (en)
NZ (1) NZ199235A (en)
ZA (1) ZA818696B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3144470A1 (en) * 1981-11-09 1983-05-19 Unilever N.V., 3000 Rotterdam FOAM CONTROLLED DETERGENTS
ZA833292B (en) * 1982-05-11 1984-12-24 Unilever Plc Granules containing silicone-based anti-foam and a process for preparing them
GB8619683D0 (en) * 1986-08-13 1986-09-24 Unilever Plc Particulate ingredient
JPH02113117U (en) * 1989-02-28 1990-09-11
GB2238530A (en) * 1989-10-31 1991-06-05 Grace W R & Co Antifoaming and defoaming compositions
EP2678410B1 (en) 2011-02-17 2017-09-13 The Procter and Gamble Company Composiitons comprising mixtures of c10-c13 alkylphenyl sulfonates

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1128330A (en) * 1965-01-08 1968-09-25 Unilever Ltd Detergent composition
NO121968C (en) * 1966-06-23 1977-06-13 Mo Och Domsjoe Ab
GB1571502A (en) * 1976-01-23 1980-07-16 Unilever Ltd Detergent compositions
ZA807664B (en) * 1979-12-14 1982-07-28 Unilever Ltd Process for making detergent compositions

Also Published As

Publication number Publication date
AU7856281A (en) 1982-06-24
AU549669B2 (en) 1986-02-06
DE3164235D1 (en) 1984-07-19
FI813990L (en) 1982-06-18
AR225124A1 (en) 1982-02-15
EP0054436A1 (en) 1982-06-23
JPS57125299A (en) 1982-08-04
FI67400C (en) 1985-03-11
BR8108146A (en) 1982-09-28
CA1163522A (en) 1984-03-13
ZA818696B (en) 1983-07-27
EP0054436B2 (en) 1989-01-25
JPS6110515B2 (en) 1986-03-29
EP0054436B1 (en) 1984-06-13
ATE7928T1 (en) 1984-06-15
DK558981A (en) 1982-06-18
FI67400B (en) 1984-11-30
NO814304L (en) 1982-06-18

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