GB2321253A - Liquid detergent formulation - Google Patents

Liquid detergent formulation Download PDF

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Publication number
GB2321253A
GB2321253A GB9700803A GB9700803A GB2321253A GB 2321253 A GB2321253 A GB 2321253A GB 9700803 A GB9700803 A GB 9700803A GB 9700803 A GB9700803 A GB 9700803A GB 2321253 A GB2321253 A GB 2321253A
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United Kingdom
Prior art keywords
formulation
alkyl
sulphate
weight
amount
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
GB9700803A
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GB9700803D0 (en
GB2321253B (en
Inventor
Helen Elizabeth Herd
Caroline Lorraine Ashton
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.)
Robert McBride Ltd
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Robert McBride Ltd
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Publication date
Application filed by Robert McBride Ltd filed Critical Robert McBride Ltd
Priority to GB9700803A priority Critical patent/GB2321253B/en
Publication of GB9700803D0 publication Critical patent/GB9700803D0/en
Priority to EP98300040A priority patent/EP0854182A3/en
Publication of GB2321253A publication Critical patent/GB2321253A/en
Application granted granted Critical
Publication of GB2321253B publication Critical patent/GB2321253B/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/94Mixtures with anionic, cationic or non-ionic 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
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/29Sulfates of polyoxyalkylene ethers
    • 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
    • C11D1/662Carbohydrates or derivatives
    • 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
    • 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
    • C11D1/75Amino oxides
    • 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
    • C11D1/88Ampholytes; Electroneutral compounds
    • C11D1/90Betaines

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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)

Abstract

A liquid detergent formulation comprising for use as a "washing-up" liquid comprises, by weight, 10-20% of an alkyl (C 8-22 ) sulphate, 1-10% of an alkyl (C 8-22 ) ether sulphate, 1-7% of an amine oxide containing at least one C 8-22 alkyl group, 1-7% of an amphoteric betaine surfactant containing at least one C 8-22 alkyl group, 1 to 15% of an ethoxylated alcohol (C 8-22 ), and a balance of water. An alkyl polyglycoside and a xylene sulphonated hydrotrope may also be included. Preferred surfactants indicated are sodium lauryl sulphate and sodium lauryl ether sulphate the fatty alcohol ethoxylate lufensol ON80, a Cocoamideopropyl betaine and dialkyl dimethyl amine oxide.

Description

1 DETERGENT FORMULATION 2321253 The present invention relates to a
detergent formulation intended particularly but not exclusively as a so-called "washing-up" liquid for use in washing crockery, cutlery, pans and other domestic utensils which have been used in the preparation and/or consumption of food and which have deposits of food, grease, burnt residues etc.
Purchasers of "washing-up" liquids generally regard two particular properties as being of importance. One is that a relatively small quantity of the liquid will suffice for washing a particular number of utensils. In other words, the purchasers like to feel that the liquid is economical to use. The other property is that the liquid generates a relatively large volume of suds (i.e. the liquid has a good lathering characteristics) since it is generally assumed that such suds contribute to the efficiency of the liquid.
GB-A-2 290 301 discloses "washing-up" liquid having good cleaning and lathering performance without the use of LABS (linear alkyl benzene sulphonic acid usually used as the sodium salt) or diethanolarnides (which are associated with nitrosamines). The present invention aims to provide detergent formulations demonstrating improved performance.
According to the present invention there is provided a liquid detergent formulation comprising, by weight, 10-20% of an alkyl (C8-22) sulphate, 110% of an alkyl (C8-22) ether sulphate, 1-7% of an amine oxide containing at least one C8-22 alkyl group, 1-7% of an amphoteric betaine surfactant containing at least one C8-22 alkyl group, 1 to 15% of an ethexylated alcohol (C8-22), and a balance of water.
2 One difference between the formulation of the present invention and that of GB-A-2 290 301 is the inclusion in the former of 1-10% of an alkyl ether sulphate. We have found that this inclusion serves to provide an improvement in performance.
The composition of the invention includes at least one C8-22 alkyl sulphate used in an amount of 10-20% by weight of the formulation, more preferably 12-18%, even more preferably 15-17%.
The alkyl sulphate is preferably an alkali metal alkyl sulphate with the preferred alkali metal being sodium.
For preference, the alkyl group of the alkyl sulphate has 8-16 carbon atoms. The alkyl sulphate may be a single compound (preferably C12) or may comprise a mixture of alkyl sulphates of different chain lengths, preferably with C12 predominating. For preference the alkyl groups are primary alkyl groups and preferably straight chain.
The carbon chain of the alkyl sulphate may be produced synthetically or may be derived from natural products (e.g. coconut oil) so that the chain length distribution of the alkyl group will correspond to that in the natural product from which it is derived.
The alkyl sulphate may be a"narrow cut" lauryl sulphate having carbon chains -1 1 principally Of C12 to C14 (C12 predominating), e.g. 60-70% C12, 20-30% C 4 PIUS minor amounts of Cl 0 and C 16.
A preferred alkyl sulphate is available under the name Empicol LX28 (Albright & Wilson).
3 The alkyl (C8-22) ether sulphate is preferably used in an amount of 1-5%, e.g. 2-5%. The cation present in this material may, for example, be an alkali metal (particularly sodium) or ammonium. It is particularly preferred that the alkyl ether sulphate be an alkyl (c8-22) ethoxylated (n = 1 to 5, preferably 2 or 3) sulphate.
The alkyl group of the ether sulphate may be as described for the alkyl sulphate.
The most preferred alkyl ether sulphate for use in the invention is sodium lauryl ether sulphate where n = 2 or 3.
An alkyl ether sulphate which may be used is available under the name Empicol 0251 (Albright & Wilson).
The formulation of the invention contains 1 to 7%, more preferably 1 to 3%, of an amine oxide containing at least one CS-22 alkyl group. The amine oxide preferably has one such group Of CS-22 carbon atoms and two C1-4 alkyl groups. Most preferably the latter alkyl groups are methyl groups. Preferred amine oxides are therefore (C8-22) alkyl dimethyl amine oxides. The long chain alkyl group may, for example, have 818 carbon atoms and the compound may comprise a mixture of alkyl groups, which are preferably C 10 to C 18 (with C 12 predominating).
A suitable amine oxide is available under the name Genaminox CSX (Hoechst).
The betaine surfactant is used in the formulation of the invention in an amount of 1-7%, more preferably 1-4%. Preferred betaines may be either of the formula (1) or (11).
4 R 1 R 3-N-CH2-COO- 1 (1) R- R 1 1 R 3 CONHCH2CH2CH2N±CH2C00- 1 (11) K_ In the above formula, R' and R2 may be the same or different C 1-4 alky 1 groups whereas R3 is an alkyl group having 8-22 carbon atoms, e.g. mixed C10 to C14.
The preferred betaine for use in the formulation of the invention is cocoamidopropyl betaine.
A suitable betaine is available under the name Rewoteric AMB14 (Witco).
A further component of the formulation of the invention is the ethoxylated alkanol (C8-22) which is used in an amount of 1- 15%, more preferably 6-10%.
Examples of such ettioxylated alkanols which may be used are those in which the alkanol (from which the product is derived) is a primary alcohol and is preferably linear. Preferably the alkanol has 6 to 11 carbon atoms (e.g. mixed C9-C) j) and in which the degree of ethoxylation is 5-15 (particularly 8-10).
A suitable fatty alcohol ethoxylate is available under the name Lutensol ON80 (BASF).
Formulations in accordance with the invention may additionally contain an alkyl (C8-22) polyglycoside which is an acetal of glucose with a primary alcohol (e.g. C12-CI4). If present, the preferred amount of the alkyl polyglycoside is up to 33%, e.g. 0. 1 to 1.5% by weight.
A suitable polyglycoside is available under the name Glucopan 60OCSUP (Henkel).
A further optional component which may be used in the formulation of the invention is a hydrotrope which may be used in an amount up to 4%, e.g. 0. 5-2%, of the formulation. A particular preferred hydrotrope is sodium xylene sulphonate.
The formulation may contain the usual minor addition such as preservatives, dyes and/or perfumes.
The invention will be illustrated with reference to the following nonlimiting Example.
Exampk Formulations A-D were prepared as shown below. Formulation A is generally in accordance with the teachings of GB-A-2 290 3 W 1 and is provided for the purposes of comparison. Formulations B-D are in accordance with the present invention.
6 Sodium Lauryl Sulphate (Empicol L28) Sodium Lauryl Ether Sulphate (Emplcol 025 1) Fatty Alcohol Ethoxylate (Lutensol ON80) 8.6 Cocoamidopropyl Betaine (Rewoteric AMB 14) 3.75 Dialkyl Dimethyl Amine Oxide (Genaminox CSX) 2.4 Alkyl Polyglycoside (Glucopon 60OCSUP) 0.95 Sodium Xylene Sulphonate 1.05 Preservatives, Dyes, Perfumes Water % by weight A B c D 11.8 15.96 2.0 8.5 2.1 2.1 0.05 12.6 5.0 5.0 8.0 7.0 2.1 1.95 2.1 0.8 0.5 2.0 1.6 Minor Additions to 100 toloo toloo toloo 11.2 In the above table. the percentages represent amount of active material.
The above formulations were compared for their effectiveness in washing plates and foaming (lathering) properties. The plate washing test was a standard test used to determine the number of plates which could be washed using a predetermined quantity (1.8g) of the detergent formulation. The plates had each been soiled with 2 mI of melted lard applied in the form of small drops and then allowed to harden.
Similarly the lathering performance was judged by a standard test in which 200 nil of a 1% solution of the formulation is drained into a measuring cylinder from a separating funnel positioned 75 em above the base of the cylinder. The height of the lather produced after 1 minute and after ') 0 minutes was measured.
1) Standard Platewash (Lard Soil) Total Plates Washed Hard Water 16 19 18 19 1 Soft Water 3 16 16 17 7 2) Mixed Soil Platewash Total Plates Washed 14 15.5 15 15 (Mean of 5 Soils) 3) Foam Heights Initial (ram) 112 125 126 130 minutes (cm) 101 122 121 128 ForTnulations B, C and D were also found to be significantly better at removing burnt on soil after soaking (results not shown).
It will be appreciated from the information presented above that formulations in accordance with the invention are of considerably improved performance as compared to the prior art formulation A.

Claims (30)

1. A liquid detergent formulation comprising, by weight, 10-20% of an alkyl (C822) sulphate, 1-10% of an alkyl (C8-22) ether sulphate, 1-7% of an amine oxide containing at least one C8-22 alkyl group, 1-7% of an amphoteric betaine surfactant containing at least one C8-22 alkyl group, 1 to 15% of an ethoxylated alcohol (C8-22), and a balance of water.
2. A formulation as claimed in claim 1 wherein the alkyl sulphate is present in an amount of 12-18% by weight.
3. A forTnulation as claimed in claim 2 wherein the alkyl sulphate is present in an amount of 15-17% by weight.
4. A formulation as claimed in any one of claims 1 to 3) wherein the alkyl sulphate is an alkali metal alkyl sulphate.
5. A formulation as claimed in claim 4 wherein the alkali metal is sodium.
6. A formulation as claimed in any one of claims 1 to 5 wherein the alkyl group of the alkyl sulphate has 8-16 carbon atoms.
7. A formulation as claimed in claim 6 wherein the alkyl sulphate is or is predominantly a lauryl sulphate.
8. A formulation as claimed in any one of claims 1 to 7 wherein the alkyl ether sulphate is present in an amount of 1-5% by weight.
C5 9. A formulation as claimed in claim 8 wherein the alkyl ether sulphate is present in an amount of 2-5% by weight.
9
10. A formulation as claimed in any one of claims 1 to 9 wherein the cation of the alkyl ether sulphate is an alkali metal (preferably sodium) or ammonium.
11. A formulation as claimed in any one of claims 1 to 10 wherein the alkyl ether sulphate is an alkyl ethoxylated sulphate.
12. A formulation as claimed in claim 11 wherein the alkyl ethoxylated sulphate has 1 to 5 units of ethoxylation.
13. A formulation as claimed in claim 12 wherein the alkyl ethoxylyated sulphate has 2 or 3 units of ethoxylation.
14. A formulation as claimed in claim 13) wherein the alkyl ether sulphate sodium lauryl ether sulphate.
is
15. A formulation as claimed in any one of claims 1 to 14 containing 1 to -3% of the amine oxide.
16. A formulation as claimed in any one of claims 1 to 15 wherein the amine oxide has one alkyl group Of C8-22 carbon atoms and two C] -4 alkyl groups.
17. A formulation as claimed in claim 16 wherein the amine oxide is a (C822) alkyl dimethyl amine oxide.
18. A formulation as claimed in any one of claims 1 to 17 wherein the betaine surfactant is present in an amount of 1 to 4% by weight.
19. A formulation as claimed in any one of claims 1 to 18 wherein the betaine is of the formula R 1 1 R 3_N-CH,-COO- 1 (1) R R 1 1 R'CONHCH2CH2CH2N±CH,COO- (11) in which R' and R2 may be the same or different C 1-4 alkyl groups and R 3 is an alkyl group having 8-22 carbon atoms.
20. A formulation as claimed in claim 19 wherein the betaine is cocoamidopropyl betaine.
21. A formulation as claimed in any one of claims 1 to 20 wherein the ethoxylated alcohol is present in an amount of 6-10% by weight.
22. A formulation as claimed in any one of claims 1 to 21 wherein the alkanol from which the ethoxylated alkanol is derived is linear.
23. A formulation as claimed in any one of claims 1 to 22 wherein the alkanol from which the ethoxylated alkanol is derived has 6 to 11 carbon atoms.
24. A formulation as claimed in any one of claims 1 to 23 in which the degree of ethoxylation in the ethoxylated alkanol is 5-15.
25. A formulation as claimed in claim 26 wherein said degree of ethoxylation is 810.
26. A formulation as claimed in any one of claims 1 to 25 additionally containing an alkyl WS-22) polyglycoside.
27. A formulation as claimed in claim 26 wherein the alkyl polyglycoside is present in an amount up to -3% by weight.
28. A formulation as claimed in any one of claims 1 to 27 additionally containing a hydrotrope.
29. A formulation as claimed in claim 28 wherein the hydrotrope is present in an amount up to 10% by weight.
30. A formulation as claimed in claim 28 or 29 wherein the hydrotrope is sodium xylene sulphonate.
GB9700803A 1997-01-16 1997-01-16 Liquid detergent formulation Expired - Fee Related GB2321253B (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
GB9700803A GB2321253B (en) 1997-01-16 1997-01-16 Liquid detergent formulation
EP98300040A EP0854182A3 (en) 1997-01-16 1998-01-06 Detergent formulation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9700803A GB2321253B (en) 1997-01-16 1997-01-16 Liquid detergent formulation

Publications (3)

Publication Number Publication Date
GB9700803D0 GB9700803D0 (en) 1997-03-05
GB2321253A true GB2321253A (en) 1998-07-22
GB2321253B GB2321253B (en) 2000-10-18

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1074606A2 (en) * 1999-08-03 2001-02-07 Cognis Deutschland GmbH Detergent formulation
RU2586889C1 (en) * 2015-01-12 2016-06-10 Виктор Владимирович Бочаров Liquid detergent

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2427614A (en) * 2005-06-23 2007-01-03 Reckitt Benckiser Inc Dishwashing detergent composition
CA2784780C (en) 2009-12-17 2018-01-16 Stepan Company Foaming light duty liquid detergent compositions, methods of making and uses thereof
DE102016202822A1 (en) * 2016-02-24 2017-08-24 Henkel Ag & Co. Kgaa Stabilized detergents
DE102016204062A1 (en) * 2016-03-11 2017-09-14 Henkel Ag & Co. Kgaa Amine oxide-containing cleaning agents
CN112426373B (en) * 2020-11-27 2021-07-27 佛山市南海东方澳龙制药有限公司 Pet shampoo with functions of treating ectoparasite dermatosis and resisting bacteria and preparation method thereof
EP4105304A1 (en) * 2021-06-15 2022-12-21 Henkel AG & Co. KGaA Self-thickening dilutable concentrate for hard surface & dish wash cleaning applications
EP4419639A1 (en) * 2021-10-13 2024-08-28 Unilever IP Holdings B.V. A stable liquid disinfecting composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0181212A1 (en) * 1984-11-07 1986-05-14 The Procter & Gamble Company Liquid detergent compositions
EP0232153B1 (en) * 1986-02-03 1994-08-10 Unilever Plc Detergent compositions
GB2292562A (en) * 1994-07-13 1996-02-28 Procter & Gamble Liquid Detergent Compositions
WO1996024655A1 (en) * 1995-02-09 1996-08-15 Unilever Plc Light duty cleaning compositions

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2268069B1 (en) * 1974-04-19 1977-10-14 Procter & Gamble Europ
EP0157443B1 (en) * 1984-03-19 1988-05-18 THE PROCTER & GAMBLE COMPANY Detergent composition containing semi-polar nonionic detergent, alkaline earth metal anionic detergent, and amidoalkylbetaine detergent
GB2172297B (en) * 1985-02-28 1989-06-21 Procter & Gamble Mild detergent compositions
JPH0699711B2 (en) * 1989-07-25 1994-12-07 花王株式会社 Liquid detergent composition
DE69427916T2 (en) * 1993-09-20 2002-04-04 The Procter & Gamble Company, Cincinnati THICKENED AQUEOUS DETERGENT COMPOSITION WITH IMPROVED CLEANING PERFORMANCE
GB2290301B (en) * 1994-05-31 1998-09-02 Mcbride Robert Ltd Detergent formulation

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0181212A1 (en) * 1984-11-07 1986-05-14 The Procter & Gamble Company Liquid detergent compositions
EP0232153B1 (en) * 1986-02-03 1994-08-10 Unilever Plc Detergent compositions
GB2292562A (en) * 1994-07-13 1996-02-28 Procter & Gamble Liquid Detergent Compositions
WO1996024655A1 (en) * 1995-02-09 1996-08-15 Unilever Plc Light duty cleaning compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1074606A2 (en) * 1999-08-03 2001-02-07 Cognis Deutschland GmbH Detergent formulation
EP1074606A3 (en) * 1999-08-03 2001-05-02 Cognis Deutschland GmbH Detergent formulation
RU2586889C1 (en) * 2015-01-12 2016-06-10 Виктор Владимирович Бочаров Liquid detergent

Also Published As

Publication number Publication date
EP0854182A3 (en) 1998-12-16
GB9700803D0 (en) 1997-03-05
EP0854182A2 (en) 1998-07-22
GB2321253B (en) 2000-10-18

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Effective date: 20050116