GB2206602A - Liquid laundry detergent compositions - Google Patents

Liquid laundry detergent compositions Download PDF

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Publication number
GB2206602A
GB2206602A GB08816023A GB8816023A GB2206602A GB 2206602 A GB2206602 A GB 2206602A GB 08816023 A GB08816023 A GB 08816023A GB 8816023 A GB8816023 A GB 8816023A GB 2206602 A GB2206602 A GB 2206602A
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United Kingdom
Prior art keywords
component
composition according
composition
sulphonates
fatty
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB08816023A
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GB8816023D0 (en
GB2206602B (en
Inventor
Jean-Pierre Chavannes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sandoz AG
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Sandoz AG
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Filing date
Publication date
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Publication of GB8816023D0 publication Critical patent/GB8816023D0/en
Publication of GB2206602A publication Critical patent/GB2206602A/en
Application granted granted Critical
Publication of GB2206602B publication Critical patent/GB2206602B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • C11D10/042Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap based on anionic surface-active compounds and soap
    • 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
    • C11D1/04Carboxylic acids or salts thereof
    • C11D1/06Ether- or thioether carboxylic acids
    • 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
    • C11D1/123Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • 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
    • 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
    • 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
    • C11D1/28Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
    • 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
    • C11D1/29Sulfates of polyoxyalkylene ethers

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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

11 Case 150-5186 2206602 IMPROVEMENTS IN OR RELATING TO ORGANIC COMPOUNDS
This invention relates to liquid laundry detergent compositions for use in domestic and industrial laundering.
Such liquid detergents mostly consist of a mixture of anionic and non-ionic surfactants, but no builders, so that their washing power for fatty stains is only moderate despite their high surfactant content (40 X). For good washing effect on protein-containing stains it is also necessary to include enzymes in the formulation.
According to the invention, there is provided a stable liquid builder-free detergent composition comprising the carboxymethylated or carboxyethylated reaction product of a fatty alcohol or an alkylphenol with ethylene oxide (hereinafter defined as component a); b) one or more fatty acid salts (hereinafter defined as component b); and one or more further anionic tensides (hereinafter defined as component c).
t Case 150-5186 A preferred composition according to the invention comprises:
is thereof; group; I.
a) 1-25 % of component a) b) 5-30 % of component b) c) 2-20 % of component c) and d) 25-80 % water together with sufficient alkali to bring the pH of the composition within the range from 6.5 to 8 (preferably 7-7.5, more preferably 7.5). A more preferred composition according to the invention comprises: a) 420 b) 10-25 c) 515 of component a) of component b) of-component c); and d) 40-80 % water together with sufficient alkali to bring the pH of the composition within the range from 6.5 to 8 (preferably 7 to 7.5, more preferably 7.5).
Normally components a) to c) are present in an amount in the range 20 to 50 % preferably 30 to 50 % inclusive of the composition Preferably component a) is a compound of formula I or a salt R1-0(CH2CH20)n-(R2-COOH), (1) in which R, is C822alkyl; CS-22alkenyl or C4-18alkylphenyl R2 is methylene or ethylene; is a number from 1 to 20; and is an average value from 0.1 to 1.
Compounds of formula I are known or can be made from known compounds by known methods.
Preferably R, is the C12-15alkyl residue of lauryl alcohol.
Preferably n is 4-5.
Preferably R2 is -CH2-.
1 1 Case 150-5186 Preferably the compound of formula I is the reaction product of a synthetic C12-15 lauryl alcohol with 4-5 moles of ethylene oxide, carboxymethylated with 0.8 moles of chloroacetic acid.
For the avoidance of doubt although compounds of formula I have been represented in their acid form, when the compositions of the invention are alkaline, they will be in salt form (preferably alkali metal salt form e.g. Na salt form). Therefore reference to the free acid includes such salt forms as well.
Preferred fatty acids of component b) are CS-22 unsaturated or saturated carboxylic acids, more preferably C12-18 saturated or unsaturated carboxylic acids.
Component b) can be added to compositions according to the invention as the free acid, which can be converted by the addition of alkali (e.g. NaOH, KOH or an organic base such as triethanolamine) to the salt form or they may be added directly in the salt form.
1 Preferred anionic surfactants of component c) may be any of the following conventional types: a) sulphates and sulphonates of fatty acids, fatty acid esters and fatty acid amides; b) linear or branched C5-18alkyl sulphates and sulphonates; c) sulphated ethoxylated compounds, particularly sulphated forms of any non-ionic surfactants; d) polycarboxylic acid ester sulphonates; and e) C5-18alkylbenzenesulphonates and Cl-4alkyl and 25 di-Cl- 4alkylnaphthalene sulphonates.
These compounds may be added to the composition in free acid form and converted to their salt forms by addition of alkali or added -Case 150-5186 directly in salt form.
Compositions according to the invention may contain one or more of the following additives: - a hydrotrope, a sequestering agent, a buffer,an enzyme and an optical brightener.
Preferred hydrotropes which may be present include for example urea, dicyandiamide and its derivatives, alcohols, water-soluble glycols, glycol ethers and glycol esters and Cl-4alkylbenzene sulphonates, provided that the compounds display no cloud point in distilled water up to 1001C. They act so as to prevent phase separation, that is to stabilise the liquid composition.
Preferred sequestering agents include citric acid, nitrilotriacetic acid and other complex formers.
"referred buffers which may be added to compositions according to the invention to stabilise the pH of the wash liquor in the neutral or alkali region, include sodium bicarbonate, sodium carbonate and sodium silicate.
Preferred enzymes which may be used include proteases and amylases.
Preferred optical brighteners that may be used include mono- or di-sulphonic acid stilbene derivatives.
By selection of any of these additional components, the washing effect of the liquid detergent can be adjusted according to the desired field of use. The liquid detergent compositions of the invention are primarily useful as domestic laundry detergents. Not only do they display good washing power, they also produce a soft handle on laundered cotton goods. Being phosphate-free, they are ecologically acceptable. Compositions according to the invention when used in conjunction with optical brighteners do not cause quenching of the brightener, so that acceptable grades of whiteness are obtained. The liquid compositions are stable and do not separate into two phases on storage.
w Case 150-5186 The following Examples, in which all percentages are percentages by weight of the entire composition, illustrate the invention.
Example 1
A composition comprising:
a) 12 % of the compound of formula la R-0-(CH2CH204-5-(CH2-COONa)0.8 (1a) where R is a C12-15alkyl group (the compound of formula la being added in the form of a 50 % aqueous paste); b) 15 % coco fatty acid; c) 15 % dodecylbenzene sulphonic acid; d) 5 % triethanolamine; e) 11.6 of a 30 % NaOH solution; f) 10 % ethanol; g) 1 % of an optical brightener of formula 1b, NH-G -CH=CH---NH N (1b) SO H SO H O"H--e 3 3 ?HN N CH 2 CH2 CONH2 H 2 CH2 OH 9-HN-- 0/ -CH 2CH2CONH2 H2CH20H and h) 30.4 % of demineralised water is made up by adding the components a) to g) to demineralised water stirring until a homogeneous solution is obtained at a pH of 7.5.
Examples 2 to 9 Compositions are made up as given in the Table below, in which Case 150-5186 the secondary alkane sulphonate is Hostaspur SAS, comprising secondary alkane sulphonates (obtained by sulphoxidation of n-paraffins) of the formula 2b R-f R-R so 3 Na being (2b) where R is a mixure of C13-17alkyl groups, the distribution C13 max 1 % C13-15 approx. 58 C16-17 approx. 39 7e; and C17 max. 3 X; and the optical brightener is a compound of the formula lb.
1 Components Of composition Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 EX, 8 Ex. 9 Compound of formula l& (as a 50 % aqueous paste) Coco fatty acid Oleic acid Dodecyl benzene sulphonic acid Secondary alkano sulphonate 20,0 (as a 60 % aqueous solution) Sodium lauryl other sulphate Triethanolamine NaOH (as a 30 % aqueous solution) Ethanol Optical Brightener Citric acid Nitrilotriacetic acid (as a 40 % aqueous solution) Sodium hydrogen carbonate Demineralised water 6,0 1 5,0 5,0 20,0 11,0 10,0 10,0 5,0 5,0 12,0 22,0 6,0 5,0 5,0 3,4 2,0 10,0 10,0 1,0 1,0 15,0 13,5 6,0 20,0 5,0 5,0 7,0 5,0 12,2 12,0 10,0 1,0 1,0 17,5 5,0 4,0 5,0 5,0 9,2 10,0 - 6,0 12,0 12,0 1,0 3,0 38,0 23,6 42,0 22,8 31,8 24,0 21,5 13,5 13,0 13,0 17,5 17,0 17,0 5,0 5,0 5,0 6,0 5,0 5,0 5,0 14,5 3,0 5,0 10,0 15,0 1,0 6,0 2,0 21,0 Total (in %) 100,0 100,0 100,0 100,0 100,0 100,0 100,0 100,0 r 1 _j 1 n P) (n (D -4 in C) k k-n boo 01% Application Example A Case 150-5186 The compositions of Examples 1 to 10 are tested on cotton samples bleached without optical brightener. The washing tests are carried out with 2 kg polyester as ballast in a Schulthess Super 45 (TM) washing machine on programme 4. The washing conditions are as follows:
cylinder volume amount of water amount of detergent temperature heating time washing time water hardness pH of the wash liquor 7.
43 1 17 1 8 gIl 600C about 11 min. about 15 min. 18OdH After washing, the effect of the detergent composition on the cotton samples is measured by means of a spectrophotometer (Datacolor Type 70-80) and expressed as the CIE whiteness degree (CIE publication No. 15.2).
1 9 - I- v Case 150-5186

Claims (11)

CLAIMS: -
1. A stable liquid detergent builder-free composition comprising:
a) the carboxymethylated or carboxyethylated reaction product of a fatty alcohol or an alkylphenol with ethylene oxide (hereinafter defined as component a); b) one or more fatty acid salts (hereinafter defined as component b); and c) one or more further anionic tensides (hereinafter defined 10 as component c).
2. A composition according to Claim 1 comprising:
a) 1-25 % of component a) b) 5-30 % of component b) c) 2-20 % of component c) and d) 25-80 % water together with sufficient alkali to bring the pH of the composition within the range from 6.5 to 8.
3. A composition according to Claim 2 comprising:
a) 4-20 % of component a) b) 10-25 % of component b) c) 5-15 % of component c) and d) 40-80 % water together with sufficient alkali to bring the pH of the composition within the range from 6.5 to 8.
4. A composition according to any one of the preceding claims in which component a) is a compound of formula I or a salt thereof; R,-0-(CH2CH2On(R2-COOH), (I) -Case 150-5186 in which R, is C8-22alkyl; C8-22alkenyl or C4-18alkylphenyl group; R2 is methylene or ethylene; n is a number from 1 to 20; and x is an average value from 0.1 to 1.
5. A composition according to Claim 4, in which R, is the C12-1salkyl residue of lauryl alcohol; n is 4-5; and R2 is -CH2-.
6. A composition according to Claim 5, in which the compound of formula I is the reaction product of a synthetic C12-15 lauryl alcohol with 4-5 moles of ethylene oxide, carboxymethylated with 0.8 moles of chloroacetic acid.
7. A composition according to any one of the preceding claims in which the fatty acids of component b) are CS-22 unsaturated or saturated carboxylic acids.
8. A composition according to any one of the preceding claims in which the anionic surfactants of component c) are selected from a) sulphates and sulphonates of fatty acids, fatty acid esters and fatty acid amides; b) linear or branched CS-18alkyl sulphates and sulphonates; c) sulphated ethoxylated compounds; d) polycarboxylic acid ester sulphonates; and e) Cs-lealkylbenzenesulphonates and Cl-4alkyl and di-Cl-4alkylnaphthalene sulphonates.
9. A composition according to any one of the preceding claims including one or more compounds selected from hydrotropes, sequestering agents, buffer solutions, enzymes and optical j 1 Case 150-5186 brighteners.
10. A composition substantially as herein described with reference to any one of Examples 1 to 10.
11. A liquid laundry detergent composition containing a 5 composition according to any one of the preceding claims.
Published 1985 at ne Pater. Offine. State I-louse. 6671 High Holborn, London WC1R 4TP. Further copies inay be obtained from The Patent Office,
GB8816023A 1987-07-09 1988-07-06 Stable liquid laundry detergent compositions Expired - Lifetime GB2206602B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE3722679 1987-07-09

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GB8816023D0 GB8816023D0 (en) 1988-08-10
GB2206602A true GB2206602A (en) 1989-01-11
GB2206602B GB2206602B (en) 1991-07-03

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GB8816023A Expired - Lifetime GB2206602B (en) 1987-07-09 1988-07-06 Stable liquid laundry detergent compositions

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JP (1) JPS6431900A (en)
CH (1) CH676604A5 (en)
FR (1) FR2617862B1 (en)
GB (1) GB2206602B (en)
IT (1) IT1226803B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0457965A1 (en) * 1990-05-25 1991-11-27 Hüls Aktiengesellschaft Low foaming washing-machine detergents
US5269960A (en) * 1988-09-25 1993-12-14 The Clorox Company Stable liquid aqueous enzyme detergent
NL9401510A (en) * 1994-09-16 1996-05-01 Chem Y Surfactant composition, surfactant concentrate in liquid form, and aqueous bleaching agent having increased viscosity and cleaning activity

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0794674B2 (en) * 1988-04-30 1995-10-11 三洋化成工業株式会社 Cleaning composition
JP4820294B2 (en) * 2004-07-23 2011-11-24 松本油脂製薬株式会社 Fiber scouring composition and fiber scouring method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1169496A (en) * 1967-04-07 1969-11-05 Unilever Ltd Detergent Compositions.
GB1284791A (en) * 1969-04-02 1972-08-09 Unilever Ltd Detergent
GB2076010A (en) * 1980-05-13 1981-11-25 Sandoz Products Ltd Bleach composition

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3819538A (en) * 1972-05-15 1974-06-25 Dow Chemical Co Environmentally compatible laundry detergent
DE2306069A1 (en) * 1973-02-08 1974-08-22 Henkel & Cie Gmbh Detergents having low phosphorus content - for washing natural and synthetic textiles and contg. carboxylate surfactant component and org. complexing salts for calcium ions

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1169496A (en) * 1967-04-07 1969-11-05 Unilever Ltd Detergent Compositions.
GB1284791A (en) * 1969-04-02 1972-08-09 Unilever Ltd Detergent
GB2076010A (en) * 1980-05-13 1981-11-25 Sandoz Products Ltd Bleach composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5269960A (en) * 1988-09-25 1993-12-14 The Clorox Company Stable liquid aqueous enzyme detergent
EP0457965A1 (en) * 1990-05-25 1991-11-27 Hüls Aktiengesellschaft Low foaming washing-machine detergents
NL9401510A (en) * 1994-09-16 1996-05-01 Chem Y Surfactant composition, surfactant concentrate in liquid form, and aqueous bleaching agent having increased viscosity and cleaning activity

Also Published As

Publication number Publication date
JPS6431900A (en) 1989-02-02
CH676604A5 (en) 1991-02-15
IT8848170A0 (en) 1988-07-11
FR2617862B1 (en) 1994-01-07
GB8816023D0 (en) 1988-08-10
GB2206602B (en) 1991-07-03
IT1226803B (en) 1991-02-19
FR2617862A1 (en) 1989-01-13

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PCNP Patent ceased through non-payment of renewal fee

Effective date: 19940706