GB2130237A

GB2130237A - Liquid detergent compositions

Info

Publication number: GB2130237A
Application number: GB08330368A
Authority: GB
Inventors: Appaya Raghunath Naik
Original assignee: Unilever PLC
Current assignee: Unilever PLC
Priority date: 1982-11-16
Filing date: 1983-11-14
Publication date: 1984-05-31
Also published as: DE3369343D1; DK523383A; EP0112045A1; AU550658B2; EP0112045B1; AU2136383A; GR81252B; NO834151L; CA1220694A; ATE25101T1; NZ206210A; BR8306255A; DK523383D0; PH18169A; JPS59126500A; GB2130237B; GB8330368D0; ZA838428B; IN158158B; JPS6050399B2

Abstract

A high-foaming liquid detergent composition, suitable inter alia for hand dishwashing, contains from 2 to 60% by weight of an active detergent system including a dialkyl sulphosuccinate (at least 2%), and also contains an added magnesium salt providing from 0.02 to 0.24% by weight of magnesium ions. The last-mentioned ingredient gives improved product stability, as demonstrated by a lower clear point, and increased viscosity at low concentrations, as well as enhanced soft water foaming performance.

Description

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GB 2 130 237 A

SPECIFICATION Detergent compositions

The present invention relates to high-foaming liquid detergent compositions suitable for use in fabric washing, shampoos, and above all, in manual dishwashing operations in both hard and soft water.

The term "dishes" as used herein means any utensils involved in food preparation or consumption which may be required to be washed to free them from food particles and other food residues, greases, proteins, starches, gums, dyes, oils and burnt organic residues.

GB 1 429 637 (Unilever) discloses hand dishwashing compositions containing as detergent-active material a water-soluble salt of a di(C7—Cg) alkyl ester of sulphosuccinic acid, in combination with an alkyl sulphate or an alkyl ether sulphate.

GB 2 108 520, GB 2 104 913, GB 2 105 325, EP 71413 and EP 71414 (Unilever) disclose high-foaming detergent compositions based on certain dialkyi sulphosuccinates, particularly those having C6 and C8 chains.

GB 1 164 854 (Shell) discloses the inclusion of 0.5 to 10% by weight of a water-soluble inorganic magnesium salt in aqueous liquid detergent compositions based on an alkyl or aryl sulphonate in conjunction with an alkyl ether sulphate or a nonionic detergent.

The present invention is based on the observation that the presence of small quantities of magnesium ions, derived from an added electrolyte, in liquid detergent compositions based on dialkyi sulphosuccinates gives both performance and formulation benefits.

The present invention accordingly provides a foaming liquid detergent composition in the form of a clear, stable aqueous solution containing from 2 to 60% by weight of active detergent comprising at least 2% by weight, preferably at least 5% by weight, based on the whole composition, of a water-soluble salt of a dialkyi sulphosuccinic acid, the composition containing at least 0.02% by weight of magnesium ions derived from an added electrolyte.

According to the invention, magnesium ions arrive in the composition as part of an added water-soluble magnesium salt, for example, magnesium sulphate, chloride, or toluene or xylene sulphonate.

The presence of magnesium ions has been found to give improved foaming performance in very soft water. This effect has already been observed with detergent-active materials other than dialkyi sulphosuccinates, for example, alkylbenzene sulphonates, but the addition of magnesium salts is generally detrimental to low-temperature product stability, causing both cloud and clear points to rise. It should be explained that the cloud point is the temperature at which clarity of the composition is lost as the external temperature is lowered; the clear point is the temperature at which a clear solution is regained as the external temperature is raised again.

Surprisingly, it has been found that the addition of low levels of magnesium salts to liquid compositions based on dialkyi sulphosuccinates actually causes a lowering of the clear point, and in relatively low-concentration formulations also increases the viscosity.

The amount of added magnesium salt is within the range of from 0.02 to 0.24% by weight of magnesium ions. The optimum level of addition within these limits for any particular formulation will depend on the total active detergent concentration, the total level and type of electrolyte present and the hydrotrope level, and can readily be determined experimentally by one skilled in the art.

The magnesium ions are added to the compositions of the invention in the form of water-soluble magnesium salts which are electrolytes. The preferred salts are magnesium sulphate and magnesium chloride. For magnesium chloride hexahydrate, the limits given above correspond to 0.17 to 2.02% by weight; for magnesium sulphate heptahydrate, the limits given above correspond to 0.21 to 2.46% by weight. Accordingly the amount of added magnesium salt present in the compositions of the invention is preferably from 0.15 to 2.50% by weight, and more preferably from 0.50 to 1.50% by weight.

The total active detergent level of the compositions of the invention can range from 2 to 60% by weight, preferably from 5 to 40% by weight. The addition of magnesium salts in accordance with the invention is especially beneficial at total active detergent levels of 30% by weight and below. At the low end of the concentration range, 20% and below, the additional benefit of viscosity increase is observed. Thus the present invention alleviates the problem of low viscosities that can arise with low-active-detergent dialkyi sulphosuccinate-based compositions.

The dialkyi sulphosuccinate, which is an essential detergent-active material in the composition of the invention, may be either symmetrical (both alkyl groups the same) or unsymmetrical. It may if desired be constituted by a mixture of materials of different chain lengths, of which the individual dialkyi sulphosuccinates themselves may be either symmetrical or unsymmetrical.

The detergent-active dialkyi sulphosuccinates are compounds of the formula I:

CH2—CH—SOgX,

I I (I)

COOR, COOR2

wherein each of R, and R2, which may be the same or different, represents a straight-chain or

GB 2 130 237 A

branched-chain alkyl group having from 3 to 12 carbon atoms, preferably from 4 to 10 carbon atoms and more preferably from 6 to 8 carbon atoms, and X, represents a solubilising cation, that is to say, any cation yielding a sait of the formula I sufficiently soluble to be detergent-active. In the context of the present invention, the solubilising cation X, will generally be monovalent, for example, alkali metal, 5 especially sodium; ammonium; or substituted ammonium, for example, ethanolamine. 5

The alkyl groups R, and R2 in the dialkyi sulphosuccinate are preferably straight-chain or (in mixtures) predominantly straight-chain.

Among dialkyi sulphosuccinates that may advantageously be used in the composition of the invention are the C6/C8 unsymmetrical materials described and claimed in GB 2 105 325 (Unilever); 10 the dioctyl sulphosuccinate/dihexyl sulphosuccinate mixtures described and claimed inGB2104 913 10 (Unilever) and the mixtures of symmetrical and unsymmetrical dialkyi sulphosuccinates described and claimed in GB 2 108 520 (Unilever).

The composition of the invention may of course with advantage contain other detergent-active agents in addition to the dialkyi sulphosuccinate, provided that the total composition contains at least 15 2% by weight, preferably at least 5%, of dialkyi sulphosuccinate(s). The composition may, for example, 15 include one or more of the sulphonate-type detergents conventionally used as the main detergent-active agent in liquid compositions, for example, alkylbenzene sulphonates (especially Cg—C15 linear alkylbenzene sulphonates), secondary alkane sulphonates, alpha-olefin sulphonates, alkyl glyceryl ether sulphonates, and fatty acid ester sulphonates. Of course dialkyi sulphosuccinates are themselves 20 sulphonate-type detergents. If such additional sulphonate-type materials are present, the total 20

sulphonate preferably predominates in the active detergent mixture of the composition of the invention. If no such additional sulphonate-type materials are present, the sulphosuccinate alone preferably predominates.

Among the additional sulphonate-type detergents that may be present, alkylbenzene sulphonates 25 and secondary alkane sulphonates are especially preferred. The ratio of dialkyi sulphosuccinate to 25

alkylbenzene sulphonate or secondary alkane sulphonate is preferably within the range of from 4:1 to 0.1:1, more preferably from 2.5:1 to 1:1.

Our copending application of even date, claiming priority from British Patent Application No.

82 32643 filed on 16 November 1982, describes and claims liquid detergent compositions containing 30 dialkyi sulphosuccinate, alkylbenzene sulphonate and/or secondary alkane sulphonate, and alkyl ether 30 sulphate.

If desired there may also be present one or more primary or secondary alkyl sulphates. If present,

these together with any sulphonate material as mentioned above, including the dialkyi sulphosuccinate, preferably predominate in the active detergent mixture of the composition of the 35 invention. 35

The composition of the invention advantageously contains one or more further detergent-active materials in addition to the dialkyi sulphosuccinate and optional additional sulphonate already mentioned. Preferably there are present one or more alkyl ether sulphates and/or one or more ethoxylated nonionic detergents having an alkyl chain length of C8 to C15 and an average degree of 40 ethoxylation of from 5 to 14. 40

Preferred alkyl ether sulphates are materials of the general formula

R3—0—(CH2CH20)n—S03X2

wherein R3 is a C10 to C18 alkyl group, X2 is a solubilising cation, and n, the average degree of ethoxylation, is from 1 to 12. R3 is preferably a C1t to C15 alkyl group and n is preferably from 1 to 8. 45 In any given alkyl ether sulphate, a range of differently ethoxylated materials, and some 45

unethoxylated material, will be present and the value of n represents an average. The unethoxylated material is, of course, alkyl sulphate. If desired, additional alkyl sulphate may be admixed with the alkyl ether sulphate, to give a mixture in which the ethoxylation distribution is more weighted towards lower values.

50 It is especially preferred to use alkyl ether sulphates containing less than 20% by weight of C14 50

and above material, as described and claimed in our copending application of even date, claiming priority from British Patent Application No. 82 32686 filed on 16 November 1982.

Examples of preferred ether sulphates for use in the present invention are Dobanol (Trade Mark) 23-3 and Dobanol (Trade Mark) 23-2 ex Shell, both based on C12 to C13 (50% of each) primary alcohol 55 (about 75% straight chain, 25% 2-methyl branched), and having average degrees of ethoxylation n of 3 55 and 2 respectively.

The ratio of dialkyi sulphosuccinate, plus any other sulphonate-type detergent present plus any alkyl sulphate present other than that intrinsically present in the ether sulphate, to ether sulphate, is preferably within the range of from 5:1 to 0.5 to 1, more preferably from 3:1 to 1:1.

60 Nonionic detergents that may be used in the composition of the invention include short-chain 60

high-foaming ethoxylated alcohols of the general formula III:

R4—0—(CH2CH20)m—H

(III)

3

GB 2 130 237 A 3

wherein R4 is an alkyl group, preferably straight-chain, having from 8 to 12 carbon atoms, and the average degree of ethoxylation m is from 5 to 12.

The weight ratio of alkyl ether sulphate to nonionic detergent is preferably at least 1:1 and more preferably within the range of from 1.5:1 to 3:1, especially about 2:1. An especially preferred nonionic 5 detergent is Dobanol (Trade Mark) 91-8 ex Shell, in which R4 is C9—C,, (predominantly straight-chain) and m is 8.

Advantageously the compositions of the invention include within their active detergent mixture a C10—C18 carboxylic acid (C2—C3 alkanol)amide, preferably a diethanolamide. The inclusion of this material, at a level not exceeding 30% by weight of the active detergent mixture, gives both 10 performance and formulation advantages. Our copending application of even date, claiming priority from British Patent Application No. 82 32688 filed on 1 6 November 1982, describes and claims liquid detergent compositions containing a dialkyi sulphosuccinate, an alkyl ether sulphate and/or a nonionic detergent, and a C10—C18 carboxylic acid di(C2—C3)alkanolamide, the last-mentioned component being present in an amount not exceeding 30% by weight of the total active detergent present. 15 As well as active detergent, magnesium ions and water, the composition of the invention will generally need to contain one or more hydrotropes. These are materials present in a formulation to control solubility, viscosity, clarity and stability, but which themselves make no active contribution to the performance of the product. Examples of hydrotropes include lower aliphatic alcohols, especially ethanol; urea; lower alkylbenzene sulphonates such as sodium toluene and xylene sulphonates; and 20 combinations of these. Hydrotropes are expensive and take up room in a formulation without contributing to its performance, and it is therefore desirable to use as small quantities of them as possible.

The compositions of the invention may also contain the usual minor ingredients such as perfume, colour, preservatives and germicides.

25 The liquid detergent compositions of the invention, containing 2 to 60% by weight of active detergent in clear, stable aqueous solution, may be used for all normal detergent purposes where foaming is advantageous, for example, fabric washing products, general purpose domestic and industrial cleaning compositions, carpet shampoos, car wash products, personal washing products, shampoos, foam bath products, and, above all, manual dishwashing.

30 The invention is further illustrated by the following non-limiting Examples.

Examples 1 and 2

The cloud points, clear points and viscosities of formulations containing dialkyi sulphosuccinate and ether sulphate, at a total active-detergent level of 24%, with 12% urea as hydrotrope, were compared at different levels of magnesium chloride hexahydrate.

35 The dialkyi sulphosuccinate used was a statistical mixture (mole ratio 1:2:1) of di-n-octyl sulphosuccinate n-hexyl n-octyl sulphosuccinate and di-n-hexyl sulphosuccinate, prepared from a 1:1 mixture of n-hexanol and n-octanol by the method described in Example 1 of GB 2 108 520 (Unilever). This material contained 2.5% of sodium sulphate in a 40% solution, so that in the formulations the sodium sulphate level was 1% by weight.

40 The ether sulphate used was Dobanol 23-2S ex Shell (50% C12, 50% C13; n=2; sodium salt).

The magnesium was added in the form of magnesium chloride hexahydrate.

The results were as follows:

A

1

2

Sulphosuccinate

16

45

Dobanol 23-2S

8

Urea

12

MgCI2. 6H20

—

0.5

1.0

Cloud point (°C)

-8

-5

3

Clear point (°C)

13.5

-1

7

50

Viscosity (cp)

153

166

162

Although the cloud point rose slightly with increasing magnesium ion level, the clear point was depressed considerably at 0.5% MgC!2. 6H20, (0.06% Mg2+) giving an advantage in terms of product stability; at 1.0% MgCI2 . 6H20 (0.12% Mg2+) this advantage was smaller, and was offset by the rise in the cloud point. There was no significant effect on viscosity.

55 Examples 3 and 4

Examples 1 and 2 were repeated using a dialkyi sulphosuccinate sample containing a lower level (1 %) of sodium sulphate, so that the overall level of that material in the composition was only 0.4% by weight. At this lower electrolyte level the urea content could be reduced to 11%.

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GB 2 130 237 A 4

The results were as follows:

B 3 4

Sulphosuccinate 16 16 16

Dobanol 23-2S 8 8 8

5 Urea 11 11 11 5

MgCI2.6H20 — 0.5 1.0

Cloud point (°C) —9 —8 —4

Clear point (°C) 15 14 2

It will be seen that at this lower electrolyte level, a higher amount of magnesium chloride 10 hexahydrate was required to effect a significant lowering of the clear point. 10

Examples 5 and 6

Examples 3 and 4 were repeated using Dobanol 23-2A (the corresponding ammonium salt)

instead of Dobanol 23-2S. The results were as follows:

15

20

Sulphosuccinate Dobanol 23-2A Urea

MgCI2. 6H20

C 16 8

10

5 16 8

10 0.5

Cloud point (°C) Clear point (°C)

-8 8

-4 0.5

6 16 8 10 1.0

15

4

6.5

20

As can be seen, the use of the ammonium salt of the ether sulphate instead of the sodium salt, at the same total electrolyte level, decreased the level of MgCI2 . 6H20 required to give a clear point lowering from 1.0 to 0.5%, the level of 1.0% now being higher than optimum.

Example 7 and 8

25 Examples 1 and 2 were repeated using a dialkyi sulpho-succinate sample free of electrolyte 25

(sodium sulphate). The urea level was 10%.

The results were as follows:

D

7

8

Sulphosuccinate

16

Dobanol 23-2S

8

Urea

10

MgCI2. 6H20

—

0.5

1.0

Cloud point (°C)

-9

-7

0

Clear point (°C)

15

16

2

35 It can be seen that a magnesium chloride level of 0.5% was insufficient to lower the clear point, 35 but the higher level of 1.0% was effective.

Example 9

This Example demonstrates the improvement in soft-water foaming performance obtained by the addition of magnesium chloride hexahydrate to a dialkyi sulphosuccinate/ether sulphate formulation. 40 The comparison was carried out by means of a plate-washing test in 1 °H (French hardness) 40

water.

In the test, plates soiled with a standard starch/fat/fatty acid mixture were washed in a standard manner with 5 litres of test solution (total concentration 1 g/iitre at 45°C) in a bowl, until only a third of the surface of the solution in the bowl was covered with foam. The number of plates washed before 45 this arbitrary end-point was reached was taken as an indicator of dishwashing and foaming 45

performance.

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GB 2 130 237 A 5

The dialkyi sulphosuccinate used was the Cg/Cg statistical mixture of Example 2, at a concentration of 16% by weight, and the ether sulphate was Dobanol 23-2S, at a concentration of 8% by weight.

This composition without added magnesium chloride hexahydrate washed 23 plates, and with 5 the addition of 1.0% by weight of magnesium chloride hexahydrate washed 27 plates. 5

Examples 10—12

This experiment shows the effect of the addition of a magnesium salt to a relatively low-concentration (16%) formulation containing a fatty acid diethanolamide in addition to a dialkyi sulphosuccinate and an alkyi ether sulphate. The dialkyi sulphosuccinate was the C6/C8 mixture used in 10 Examples 1 and 2, containing 2.5% by weight of electrolyte (sodium sulphate) in a 40% solution. The 10 alkyl ether sulphate was Dobanol 23-3A, and the fatty acid diethanolamide was Empilan (Trade Mark) CDE ex Albright & Wilson, a coconut diethanolamide.

The results are shown in the following Table. All three levels of magnesium salt were effective in lowering the clear and cloud points, and all three levels raised the viscosity, the level of 1.0% being 15 optimum in this latter respect. 15

E

10

11

12

Sulphosuccinate

8

Dobanol 23-3A

4

Empilan CDE

4

Urea

8

MgCI2. 6H20

—

0.5

1.0

1.5

Cloud point (°C)

-7

-8

Clear point (°C)

3

—

Viscosity

50

113

133

104

25 Examples 13 and 14 25

The procedure of Examples 10—12 was repeated using a formulation having the same total active detergent level (16%) but containing a higher proportion (10%) of the dialkyi sulphosuccinate. In this case a magnesium salt level of 0.5% was found to give optimum benefits.

F

13

14

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Sulphosuccinate

10

Dobanol 23-3A

3

Empilan CDE

3

Urea

8

MgCI2.6H20

—

0.5

1.0

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Cloud point (°C)

-5

-8

1

Clear point (°C)

g

—

3

Viscosity (cp)

44

90

86

Examples 15 and 16

This experiment illustrates the effect of the addition of a magnesium salt on a relatively low-40 concentration (18%) formulation containing an alkylbenzene sulphonate (Dob (Trade Mark) 102 ex 40 Shell) in addition to dialkyi sulphosuccinate and alkyl ether sulphate. The dialkyi sulphosuccinate was as used in Examples 10—14.

G

15

16

Sulphosuccinate

10

Dob 102

4

Dobanol 23-3A

4

Urea

10

MgCI2. 6H20

—

0.5

1.0

Cloud point (°C)

-7

-2

Clear point (°C)

10

2.5

Viscosity (cp)

27

60

104

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Both levels of magnesium chloride raised the viscosity, the higher lever of 1.0% being more effective. At 10% the clear point was also lowered, at the cost of a rise in the cloud point.

Examples 17 and 18

The procedure of Examples 15 and 16 was repeated at a slightly higher total active detergent 5 level (20%).

H

17

18

Sulphosuccinate

10

Dob 102

4

Dobanol 23-3A

6

Urea

10

MgCI2. 6H20

—

0.5

1.0

Cloud point (°C)

<-10

-8

Clear point (°C)

—

4.5

Viscosity (cp)

93

129

142

15 Comparative Composition H already had excellent low-temperature stability. The addition of 15

0.5% magnesium chloride increased the viscosity without detriment to the cloud point. The higher level of magnesium chloride (1.0%) improved the viscosity further to the slight, but insignificant, detriment of the low-temperature stability.

Claims

Claims

20 1 • A foaming liquid detergent composition in the form of a clear, stable aqueous solution 20

containing from
2 to 60% by weight of an active detergent mixture comprising at least 2% by weight,

based on the total composition, of a water-soluble salt of a dialkyi ester of sulphosuccinic acid, wherein the composition further comprises from 0.02 to 0.24% by weight of magnesium ions derived from an added electrolyte.

25 2. A detergent composition as claimed in claim 1, which comprises from 0.15 to 2.50% of an 25

added inorganic magnesium salt selected from magnesium sulphate, magnesium chloride and mixtures thereof.
3. A detergent composition as claimed in claim 2, which comprises from 0.50 to 1.50% by weight of the added magnesium salt.

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4. A detergent composition as claimed in any one of claims 1 to 3, wherein the total 30

concentration of active detergent is within the range of from 5 to 40% by weight.
5. A detergent composition as claimed in claim 4, wherein the total concentration of active detergent is within the range of from 5 to 30% by weight.
6. A detergent composition as claimed in claim 5, wherein the total concentration of active

35 detergent is within the range of from 5 to 20% by weight. 35
7. A detergent composition as claimed in any one of claims 1 to 6, wherein the dialkyi sulphosuccinate constitutes at least 5% by weight of the total composition.
8. A detergent composition as claimed in any one of claims 1 to 7, wherein the alkyl groups of the dialkyi sulphosuccinate each have from 4 to 10 carbon atoms.

40
9. A detergent composition as claimed in claim 8, wherein the alkyl groups of the dialkyi 40

sulphosuccinate each have from 6 to 8 carbon atoms.
10. A detergent composition as claimed in any one of claims 1 to 9, wherein the active detergent mixture further comprises an alkylbenzene sulphonate and/or a secondary alkane sulphonate.
11. A detergent composition as claimed in claim 10, wherein the weight ratio of dialkyi

45 sulphosuccinate to alkylbenzene sulphonate and/or secondary alkane sulphonate is within the range of 45 from 2.5:1 to 1:1.
12. A detergent composition as claimed in any one of claims 1 to 11, wherein the active detergent mixture further comprises a C10 to C18 alkyl polyethoxy sulphate having an average degree of ethoxylation of from 1 to 12.

50
13. A detergent composition as claimed in claim 12, wherein the alkyl polyethoxy sulphate has 50

an alkyl chain length of Cn to C15.
14. A detergent composition as claimed in claim 12 or claim 13, wherein the alkyl polyethoxy sulphate contains less than 20% by weight of material of chain length of C14 and above.
15. A detergent composition as claimed in any one of claims 12 to 14, wherein the weight ratio

55 of dialkyi sulphosuccinate, plus any alkylbenzene sulphonate and/or secondary alkane sulphonate 55

present, to alkyl polyethoxy sulphate is within the range of from 5:1 to 0.5:1.
1 6. A detergent composition as claimed in any one of claims 1 to 15, wherein the active

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GB 2 130 237 A 7

detergent mixture further comprises a C10—C18 carboxylic acid di(C2—C3 alkanol)amide, in an amount not exceeding 30% by weight of the active detergent mixture.
17. A detergent composition as claimed in claim 1, wherein the active detergent system consists essentially of:

5 a) (i) a water-soluble salt of a dialkyi sulphosuccinic acid in which the alkyl groups may be the 5 same or different, and, optionally,

(ii) an alkylbenzene sulphonate and/or a secondary alkane sulphonate,

and b) (i) a C10—C18 alkyl polyethoxy sulphate having an average degree of ethoxylation of from 1 to

10 12, and, optionally, 10

(ii) a C8—C15 ethoxylated nonionic surfactant having an average degree of ethoxylation of from 5 to 14, the weight ratio of (b)(i) to (b)(ii) being at least 1:1,

the weight ratio of (a) to (b) being within the range of from 5:1 to 0.5:1, and, optionally,

c) a C10—C18 carboxylic acid di(C2—C3 alkanol)amide, in an amount of from 0 to 30% by weight

15 of the total active detergent system. 15
18. A detergent composition as claimed in claim 1, substantially as described in any one of Examples 1 to 18 herein.

Printed for Her Majesty's Stationery Office by the Courier Press, Leamington Spa, 1984. Published by the Patent Office, 25 Southampton Buildings, London, WC2A 1 AY, from which copies maybe obtained.